Abstract
The activity of the hypothalamus-pituitary-thyroid axis (HPT) is coordinated by hypophysiotropic thyrotropin releasing hormone (TRH) neurons present in the paraventricular nucleus of the hypothalamus. Hypophysiotropic TRH neurons act as energy sensors. TRH controls the synthesis and release of thyrotropin, which activates the synthesis and secretion of thyroid hormones; in target tissues, transporters and deiodinases control their local availability. Thyroid hormones regulate many functions, including energy homeostasis. This review discusses recent evidence that covers several aspects of TRH role in HPT axis regulation. Knowledge about the mechanisms of TRH signaling has steadily increased. New transcription factors engaged in TRH gene expression have been identified, and advances made on how they interact with signaling pathways and define the dynamics of TRH neurons response to acute and/or long-term influences. Albeit yet incomplete, the relationship of TRH neurons activity with positive energy balance has emerged. The importance of tanycytes as a central relay for the feedback control of the axis, as well as for HPT responses to alterations in energy balance, and other stimuli has been reinforced. Finally, some studies have started to shed light on the interference of prenatal and postnatal stress and nutrition on HPT axis programing, which have confirmed the axis susceptibility to early insults.
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1 Introduction
Thyrotropin releasing hormone (TRH) is synthesized in various brain areas and in several hypothalamic nuclei [1]. The hypophysiotropic TRHergic neurons are those localized in the paraventricular nucleus (PVN) of the hypothalamus that send projections into the external layer of the median eminence, from where they release TRH into the portal vessels [2]. In rat, TRH hypophysiotropic neurons are localized in the medial and caudal zones of the PVN. TRH neurons of the anterior part of the PVN send projections to other brain areas [3]; in mouse PVN hypophysiotropic TRH neurons are located in the anterior-medial zones [2]. The PVN TRH neurons receive afferents from various brain areas that transmit signals from the internal milieu or from the environment, regulating not only TRH release from the nerve terminals located in the median eminence but also, TRH synthesis. Neurons in the arcuate nucleus sense a variety of hormones related to nutritional status due in part to a relatively permeable blood-brain barrier (BBB), and receive nerve inputs from hypothalamic and brain-stem nuclei engaged in energy balance. Afferents from the arcuate contact TRHergic neurons of the PVN where they release either neuropeptide Y (NPY) and agouti related protein (AgRP), or the pro-opiomelanocortin (POMC)-derived peptide, α-melanocyte stimulating hormone (αMSH), and cocaine-amphetamine related transcript (CART) [2, 4]. Environmental signals such as temperature or light are transmitted to the PVN TRH neurons through afferents arising from the brain stem or from the suprachiasmatic nucleus, respectively [1, 5]. Albeit less characterized, the limbic system activated in response to stressful-emotional stimuli conveys information onto PVN TRH neurons [6]. In addition, the hypophysiotropic TRH neurons are one of the targets of the feedback regulation that thyroid hormones apply on the central arm of the HPT axis [2], and respond to changes in other hormonal inputs such as circulating glucocorticoids [1]. The hypophysiotropic TRHergic neurons decode thus multiple neuronal, immune and hormonal signals that regulate the synthesis and /or release of TRH [1–8].
The TRH gene is transcribed and translated in the neuronal cell body into a protein precursor that contains repeated gln-his-pro-gly sequences. The precursor is compartmentalized with convertases, carboxypeptidase E, glutaminyl cyclase and peptidyl-glycine α-amidating monooxygenase in secretory granules that are transported to nerve terminals; the time taken for protein synthesis, and granule transport (0.5–1 um/s) to nerve terminal takes at least 2 h [1, 2, 9, 10] (Fig. 1a). Nerve terminals containing TRH are concentrated at the external layer of the median eminence, in close proximity with the cytoplasmic extensions of β-2 tanycytes, and with the portal hypothalamus-pituitary capillaries [11] (Fig. 1b, c). Both α and β tanycytes are the locus of enzymes involved in HPT regulation. One of these enzymes is deiodinase 2 (D2), which converts T4 to T3 (Fig. 1c, d) [1, 2, 12]. Another is TRH degrading ectoenzyme (Trhde), also named pyroglutamyl peptidase II (PPII), according to its catalytic activity [13, 14]. The expression of PPII in β2 tanycytes, including its cytoplasmic extensions into the median eminence, suggests that the protein is localized at the cell surface, near TRH terminals and able to degrade TRH released into the intercellular space of the median eminence. Consistent with this hypothesis, the specific activity of PPII is relatively high in the median eminence, and PPII inhibition increases TRH recovery from the extracellular medium of median eminence incubated in vitro. The peripheral injection of a specific inhibitor of PPII enhances TSH levels in cold stressed rats, which supports that PPII controls the amount of TRH that reaches the anterior pituitary [13]. The narrow specificity of PPII suggests that TRH is its only substrate in vivo, and that PPII may be critical for the control of the amplitude/duration of TRH effects. PPII is also expressed in the pituitary (in lactotrophs), and the liver expresses a soluble isoform released into the circulation (termed thyroliberinase) [15, 16].
When TRH reaches the pars distalis of the pituitary, it regulates cells that express TRH receptor-1 (TRH-R1), such as the thyrotrophs (Fig. 1c), lactotrophs and a fraction of somatotrophs. These cell types are subject to a multifactorial regulation that determines the extent and specificity of their response to TRH [17–19]. In thyrotrophs, TRH causes the release of TSH and simultaneously, the synthesis of Tshb, and of TSHα, the glycoprotein subunit α (CGA) common to other hypophysiary hormones [20]. TRH also regulates the pattern of glycosylation of TSH that confers full biological activity at the TSH receptor in the thyroid gland [21]. Binding of TRH to TRH-R1 receptor, which is coupled to Gq/11 protein, activates phospholipase C, mobilizes calcium and activates protein kinase C [19]. Several cell lines or primary cultures have aided to identify the transduction pathways involved in TRH signaling: IP3 mobilizes intracellular calcium causing TSH release; TRH-stimulated Tshb synthesis involves the Ca-calmodulin pathway; for Tsha the PKC-MAPK pathway [17, 19]. Studies with cell lines, such as GH3, have also shown the relevance of intermittent occupancy of TRH receptor, which is consistent with ligand-induced down-regulation of TRH receptor [19, 22]. TRH binding to TRH-R1 promotes receptor phosphorylation, an event that favors its endocytosis; additionally, its mRNA is down regulated by TRH and TH, and upregulated by estrogens [19]. The ability of TRH to regulate the expression of Tshb may depend upon either the pituitary architecture, and/or paracrine factors, since it can be lost in cell culture [23].
TSH is also synthesized in the pars tuberalis of the pituitary (Fig. 1c, e), where it is not regulated by TRH [24]; instead, the photoperiod controls, through melatonin, the synthesis of TSH, not only in birds but also in several mammals including some mice strains [25, 26]. Tanycytes express the TSH-receptor (TSH-R1); primary ependymal cell cultures respond to TSH stimulation, via cAMP or phosphorylated ERK pathways, stimulating Dio2 expression [27], thus increasing the amount of T3 available to hypothalamic neurons. TSH released in a constitutive manner from the pars tuberalis also reaches the circulation; it differs in its N-glycosylation pattern from that derived from the pars distalis, and forms protein-complexes with immunoglobulin or albumin that impede its bioactivity in the thyroid gland [28].
2 Feedback control of TRH output from the hypophysiotropic neurons
The activity of hypophysiotropic TRHergic neurons is set by the negative feedback control exerted by thyroid hormones (TH), by neuronal and hormonal influences responding to the nutritional status, and by inputs activated upon acute immediate demands. Drastic situations as fasting or food restriction, inflammation, hypo- or hyper-thyroidism, change the activity of the TRH neurons and the expression of TRH either directly or indirectly throughout the combined action of distinct effectors. In the case of TH feedback, several factors and cellular components are involved.
Negative feedback by thyroid hormones is exerted at multiple levels [1, 7, 17, 29, 30]. Site-4 of Trh-gene promoter binds (Fig. 1a) thyroid hormone receptors (TRs) as monomer, homodimer, or heterodimer with retinoid acid receptor X (RXR) [30]. T3 inhibits Trh transcription through either TRα or TRβ in transfected cells but in vivo, TRβ2 is the principal receptor involved in T3 feedback effects at the PVN [31]. T3 promotes the binding of TR, histone deacetylases and corepressor NCoR to the Trh promoter; however, the mechanism of negative regulation by T3 remains elusive [30–34].
TR may interact with various other transcription factors extending, by this cross-talk, the action of other regulators [35–37]. Effects of the heterodimer TR:RXR depend on the proportion and subtype of RXR (a or b); in vivo, RXRb enhances T3-repressive action [38]. Retinoids cause central hypothyroidism in humans and rat, and inhibit in vitro TRH transcription [39]. As TH induce the synthesis of retinaldehyde dehydrogenase in tanycytes, retinoic acid availability to the nearby neurons may modify the effects of TH-TR in TRH neurons [40]. Besides RXRb, TR also heterodimerizes with PPAR and the endogenous concentration of each transcription factor directs the resultant inhibition [41]. Another family of transcription factors, the LXRα or β which are activated by oxysterols, bile acids and fatty acids [42], heterodimerize with RXR or with TR, and chromatin immunoprecipitation analyses detect LXR:TR binding to the Trh promoter; TR binds to either RXR or LXR but not to both simultaneously [43]. Support of LXR involvement at PVN level is provided by experiments with LXRαβ knock down with shRNA in newborn pups, or with LXR-KO mice that show activated HPT axis in spite of high TH circulating levels; Trh expression is increased in the PVN, as well as that of many TH responsive genes in target tissues [43, 44]. LXR has been proposed as an important transcription factor involved in multiple metabolic pathways, whose dysregulation might play an important role in the metabolic syndrome [36, 42, 45]. Cholesterol metabolites and fatty acids could, in principle, activate LXR and contribute to repress Trh and Tsh transcription, providing possible mechanistic answers to the link between obesity and HPT dysfunction [46, 47].
Entry of thyroid hormones into the brain is facilitated by transporters present at the blood-brain barrier such as the monocarboxylate transporter 8 (MCT8, exclusive for TH, and other transporters as the organic anion-transporting polypeptide 1c1 (OATP1c1); both are expressed in blood vessels and tanycytes, while neurons contain mainly MCT8 [48, 49]. Transport of T4 from brain blood vessels is facilitated by OATP1c1 in rodents [50]; T4 is taken up by tanycytes and transformed to T3 by deiodinase type 2 [48]. Although D2 activity is rapidly inhibited by T4 in several tissues, by increased degradation through the ubiquitin-proteasome pathway, this does not occur in tanycytes [51]. Increased D2 expression and activity in tanycytes leads to increased T3 available to hypophysiotropic TRH neurons and TRH synthesis down-regulation. Since D2 is not detected around the third ventricle at the level of the PVN [52], it has been hypothesized that T3 enters TRHergic neurons at the median eminence level, and is transported by retrograde flux to the soma [2]. D3, the enzyme that degrades T3, is detected in axons of neurons in the median eminence but very few of these are TRHergic [53]. TRH neurons thus sense T3 directly [2]. Dio3 mRNA has not been observed in rat or mice tanycytes in basal conditions [54], but only after T3 treatment [55]. In fact, in several organs D3 is hardly detected but induced under various conditions [56]. In organotypic cultures of medial-basal hypothalamic slices, rich in tanycytes, the stimulatory effect of T3 on Dio3 expression is inhibited by TSH; as mentioned above, TSH stimulates synthesis and activity of D2 in tanycytes [40]. Thus, the balance between D2 and D3 sets up T3 levels, depending on the particular loci where T3 acts [57].
Hypothyroidism increases the expression of Trh in the PVN, and of Dio2 in tanycytes, TSH synthesis and release from the pituitary, and decreases the expression of Mct8 in the median eminence [2, 29, 48, 55], whereas changes in the expression of arcuate peptides are controversial [55, 58]. PVN Trh mRNA values increased by hypothyroidism are normalized by peripheral administration of T4, also of T3 since when T4 levels are low T3 may enter into the brain from the circulation [55, 59–61]; a microarray analysis revealed 110 genes up or down regulated by T3 treatment in the hypothalamus [55].
T4 administration inhibits not only Trh transcription but also the expression of convertases involved in processing TRH-precursor to TRH [30, 62]. In addition, the thyroid status modulates tanycyte Trhde expression, and PPII activity in the median eminence, which are rapidly increased in response to thyroid hormone administration [13, 63]. In mice, the enhancement of PPII expression in tanycytes by T4 injection precedes the reduction of Trh mRNA levels in the PVN and is dependent on D2 [64]. Thyroliberinase, the soluble form of PPII synthesized in the liver and released to the circulation from where it likely reaches the portal vessels, is also upregulated by thyroid hormones [65, 66]. These results indicate that β2-tanycyte PPII and thyroliberinase are regulated accordingly for feedback, and may contribute to adjust the HPT axis, although a formal demonstration is missing.
At the anterior pituitary level, T3 inhibits the expression of Tshb, Tsha and Trh-r1; in contrast, it upregulates PPII activity [67, 68]. The feedback effects of thyroid hormones at the pituitary level are further complicated due to the differential effects of other players that modulate TSH synthesis and are themselves targets of TH, as TRH or TRH-R1 [7, 69, 70]. Although it was originally thought that pituitary PPII contributes to the negative feedback that TH exert on the thyroid axis, failure to detect PPII expression or activity in thyrotrophs, or to modify the effect of TRH on TSH secretion with either a PPII antisense oligonucleotide or a PPII inhibitor in cell culture, casts doubt on its role in feedback control at pituitary level [15, 71].
3 Negative energy balance and the central regulation of the HPT axis
Two situations that inhibit the thyroid axis have deserved considerable attention, fasting and the non-thyroidal illness syndrome (NTIS); these are characterized by low Trh expression in the PVN, and low TSH and T3 serum concentrations [2, 8, 72]. Injections of lipopolysacharide (LPS) produce an acute inflammation and, as NTIS, induce cytokines and NFkB, which upregulate D2 in α and β tanycytes [73–75]. The effects of inflammation extend to the TH transporters; an LPS injection decreases significantly the mRNA levels of Mct8 and Oatp1c1 in brain blood vessels but not in astrocytes or neurons, which may lead to a reduction of TH passage through the blood-brain barrier [76]. Quantification of TH levels at the cellular level is not yet possible and therefore, many of these assumptions remain untested.
In conditions of negative energy balance, the activity of the HPT axis is inhibited. Fasting or food restriction leads to profound decreases of the serum concentration of leptin, which upregulates the activity of NPY/AgRP neurons in the arcuate nucleus, peptides that inhibit the expression of Trh in the PVN [2, 77]. In addition, negative energy balance inhibits POMC neurons and the release of αMSH in the PVN, a peptide that stimulates the synthesis and release of TRH from hypophysiotropic neurons [2, 78]. A leptin injection, or the icv injection of αMSH, counteracts the decrease in PVN Trh mRNA levels induced by fasting [2, 79]. Thus, the leptin drop, relayed through these arcuate nucleus neurons, contributes to a reduction of PVN TRH neurons activity, and of Trh mRNA expression in the PVN. Furthermore, in addition to this indirect pathway, leptin can activate directly Trh expression [77]. Fasting also targets tanycytes, where it increases Dio2 expression and activity, presumably through the combined effect of increased corticosterone and decreased leptin serum concentrations [2, 80]. Parallel to fasting-induced increase in Dio2 expression, in male rats PPII expression in tanycytes and activity in the median eminence, and thyroliberinase activity are also increased, whereas that of anterior pituitary PPII is not [63]. Thus, tanycyte PPII and/or thyroliberinase may engage in the adjustment of the thyroid axis in response to fasting, and/or maintain its long-term inhibition.
4 Positive energy balance and the central regulation of the HPT axis
Many circumstances, albeit not all, that affect the activity of POMC or NPY neurons coincide with altered Trh expression; conditions that stimulate energy expenditure increase αMSH and TRH content in the PVN [1, 17] (Supplementary Table 1). An interesting dichotomy stems from studies related to obesity, since obesity is correlated with reduced expression of Pomc and with increased expression of Npy although in diet induced obesity, resistance to gain weight in different mice strains correlates with POMC [81]. Feeding rats with a high fat diet (HFD) increases body weight and the activity of the HPT axis: Trh mRNA levels, processed peptide content in the PVN as well as concentrations of circulating TH are increased in response to the HFD; these changes have been attributed to a direct effect of increased leptin on TRHergic neurons [82]. However, the same group has recently reported that inhibition of the activity of the nutrient-sensing enzyme Sirtuin 1 (silent mating type information regulation 2 homolog 1 [Sirt1]), which is increased in the hypothalamus of obese subjects and correlates with inhibited energy expenditure, causes in HFD-fed rats increases in mRNA levels of Pomc and of carboxypeptidase E in the arcuate nucleus, and peptide levels of αMSH and TRH in the PVN, parallel to reduced body weight gain and increased oxygen consumption (in high-fat fed but not in lean rats) [83].
Differences in the propensity to gain weight under a HFD led to classify rats as obesity resistant (OR) or obesity prone (OP); OR rats express higher levels of Pomc, and lower of Npy, than OP rats [84]. A similar study performed in mice shows that obesity resistance to HFD correlates with a normal activity of the HPT axis during 7 weeks. In contrast, OP mice have increased Trh and Tsh expression, normal hypothalamic Dio2 expression and activity or TH circulating levels, but altered expression of several T3-target genes in liver; both OR and OP mice have similar alterations by 27 weeks [85]. The increase in Trh and Tsh expression in the obesity prone mice seems to contradict their involvement in energy expenditure, a conclusion supported by several reports indicating that hypothalamic expression of Trh and Bdnf is higher in lean than in obese animals [86, 87]. Furthermore, a recent search of the genetic background of young adults with extreme obesity found, in the exome data, a set of genes with novel mutations (indels, nonsense and missense) which are predicted as deleterious for protein function. The TRH gene was among the genes identified by this criterion [88]. These results exemplify that basal levels of TRH or TSH measured at a given time point might not correlate with either leptin, hypothalamic D2, or arcuate peptides, nor with metabolism in TH target tissues.
The information presented so far partially supports the conclusion that hypophysiotropic TRHergic neurons are energy sensors that are inhibited in conditions of energy deficit as starvation or food restriction. In conditions of positive energy balance as in diet induced obesity, variations in experimental protocols, and the complex etiology of the disease in humans, complicate the possibility to reach a definitive conclusion. It is now evident that plastic changes are induced by metabolic cues causing synaptic rearrangements in the circuits that sense and control energy balance; for example, the melanocortin system is highly susceptible of adaptation to extreme metabolic conditions [89]. Either fasting or obesity are dynamic physiological states that alter the function of various organs, they promote the release of corticosterone, cause inflammation, revealing many more players yet to be identified. In summary, these numerous actors may affect the activity of TRHergic neurons in a multifactorial fashion [90] representing a challenge for future investigations.
5 Responses of hypophysiotropic TRH neurons to acute stimuli
Energy demanding situations as cold exposure increase very rapidly (15–60 min) PVN Trh-mRNA levels [1, 2, 91–94]. They also enhance convertase expression in the PVN [95]. Simultaneously, within minutes, the pre-existing TRH stored in median eminence terminals is released. An increase of TSH concentration in serum is detected at 30–60 min, followed by an enhancement of serum T4 concentration. T4 is converted to T3 by D2 at target tissues: in brown adipose tissue (BAT) for example, D2 activity is stimulated by sympathetic afferents; in turn, T3 increases uncoupling protein 1 (UCP-1) transcription and maintains thermogenesis [1, 96]. Increased TH levels exert feedback inhibition to normalize the activity of the axis and achieve homeostatic equilibrium. Regulation of deiodinase activities and TH effects are target specific [97]. Even if cold-exposure is maintained, PVN Trh mRNA levels normalize by the second hour [91, 98]. The rapid transcriptional response of TRHergic neurons to neuronal stimuli is elicited by the almost immediate increase in CREB phosphorylation. Stimuli that enhance CREB phosphorylation, for example by PKA or ERK activators in hypothalamic or neuroblastoma cells, increase pCREB binding to CRE-2 and stimulate TRH synthesis (Fig. 1b); [99–101]. The relevance of pCREB for Trh expression has been demonstrated in vitro [102], or in vivo in response to αMSH and other arcuate-derived peptides [103]. The transient cold-induced increased Trh expression may relate to the transiency of the kinetics of CREB activation, and to non-cell autonomous effects such as the counter-regulatory effects of corticosterone.
As reported for chronic stress, acute stress inhibits Trh synthesis and the activity of the HPT axis [1]. An acute stress previous to a cold exposure blunts the cold-induced stimulation of the HPT axis, effect reproduced by a corticosterone injection 1 h before cold stimulation which interferes with the increase in Trh mRNA levels; likewise, corticosterone blunts the enhancement of Trh mRNA levels by cAMP analogs in hypothalamic cells [96]. These results underscore the importance of timing in intracellular activation, transport and inactivation of transcription factors for the transcriptional control of Trh expression, as previously shown for CRH neurons [104]. The interfering effects of glucocorticoids on PKA signaling occur before transcription; neither pCREB nor GR bind to their response elements in the TRH gene proximal promoter when hypothalamic cells are co-incubated with dexamethasone (or corticosterone) and forskolin (or cAMP analogs) [96, 101]. Recent experiments have revealed that this interference is not due to the recruitment of deacetylases to the TRH promoter, but occurs by a protein:protein interaction between activated GR and catalytic PKA that diminishes their translocation into the nucleus in cultured cells, and decreases the phosphorylation of CREB. In vivo, the number of PVN TRHergic cells expressing pCREB increases after 1 h of cold exposure, but not if animals were previously injected with corticosterone (Sotelo et al., 2016 unpublished). These recent findings contribute to untangle the early interactions between transcription factors that regulate Trh gene expression. However, many more remain to be elucidated since for example, the CRE site is flanked by GC sites and SP1/Krüppel response elements [101] which may be activated by insulin and, depending on the type of Krüppel factor activated, it could have stimulatory or inhibitory actions on CREB binding or on Trh transcription [105].
6 Integrated responses of the HPT axis
As consequence of a meal or temporal food deprivation, leptin, insulin, ghrelin and other hormones activate or inhibit the POMC or AgRP/NPY neurons that control the HPT axis activity. These stimuli are likely transient, but necessary for maintaining homeostatic metabolic environment. Given the nocturnal nature of laboratory rodents, and that most experiments are performed during light hours, results may vary depending on the time frame [92]. Furthermore, not all effectors have been characterized and therefore, consideration of the different variables involved provides a framework to analyze and interpret the functioning of the HPT axis. How an acute response is modified by the situation of the animal at a particular time deserves attention. For example, several reports suggest that exercise inhibits the HPT axis activity; conditions of forced or exhaustive exercise decrease the levels of circulating TH levels, and it has been proposed that it is due to the increase in circulating glucocorticoids or interleukin 6 [106]. The effect of increased physical activity on the thyroid axis probably depends on the extent of the energy demand and individual reserves; 20–30 min of intense treadmill exercise causes a rapid increase in serum T4 concentration with later decreases in T3 serum concentration [107], while growth hormone (GH) is gradually increased, dependent on the increases in TH as a treatment with propyl-thiouracil avoids GH increase together with its lipolytic effects [108]. We have shown that intermittent exercise provided by voluntary wheel running increases Trh expression and activates the HPT axis proportionally to the amount of exercise performed during the last period or the 2 weeks the experiment lasted, and to the loss of white adipose tissue; lipolysis provides the required fuel that balances the diminished food intake [109]. The HPT axis appears stimulated in spite of lower serum leptin concentrations than those of the pair-fed group [109]. These assumptions are valid when data are compared to a pair fed group that was given the amount of food consumed by the exercised group and not, to naive rats fed ad libitum [109]. Since exercise is intermittent its impact on central pathways is probably so, which differs from longer-term forced situations like training exercise. Voluntary wheel running might resemble an active-mode of life, whose effects are in contrast to the sedentary style that animals encounter in an un-enriched cage [110].
In conclusion, we have provided examples of steady state conditions in hypophysiotropic PVN TRH neurons activity that reflect a balance between thyroid hormone feedback, nutrition status, and the stimulatory or inhibitory influences of the circadian cycle. These studies indicate that at a given time TRHergic neurons respond to an incoming stimulus depending on the state of the circuit engaged, which is modulated by previous influences.
7 Genetic alterations in TRH signaling
Central hypothyroidism arises from dysfunction at hypothalamic or pituitary levels. Congenital causes are being traced to mutations in the genes coding for elements involved in TRH signaling. Although adult TRH knockout mice have central hypothyroidism and a decrease in the bioactivity of TSH [111], in humans congenital causes have not been attributed to hypothalamic gene mutations [112, 113]. Only one Trh mutation has been characterized in obese young adults [88]. However, several mutations related to central hypothyroidism correspond to TRH-receptor or to other elements down the chain of participants in the activity of the HPT axis [113–115], aside from those that involve combined pituitary pathologies. Thus, rare biallelic TRH-R mutations, including a nonsense mutation and an in-frame deletion, have been associated to isolated congenital hypothyroidism with reduced circulating T4 and absent TSH response to exogenous TRH [116, 117]. Recently, a deleterious missense TRH-R mutation associated with congenital hypothyroidism mapped to the second transmembrane helix drastically reduces the ability of the receptor to signal through the Gq/11dependent pathway [115]. These results are consistent with data showing that the ablation of TRH-R1 expression in mice produces a profound central hypothyroidism [118].
A genome wide association study indicates a significant association between polymorphisms (rs16892496 and rs7832552) of the TRH-R1 gene and lean body mass in humans. Subjects carrying the theoretically highest expressing (TT) genotype in the rs7832552 single nucleotide polymorphism [according to [119]; see below] had higher lean body mass compared to the other subjects [120]. An additional study in older women is consistent with an association of the rs16892496 polymorphism with fat-free mass, and suggests additionally an association with muscle strength [121]. Recently, the functionality of some of these mutations was assessed with luciferase gene reporter assays in cell culture; these mutations show diminished activity compared to the other alleles [115, 119]. Thus, a functional link may exist between TRH-R1 gene polymorphism and lean body mass.
8 Altering the programming of the HPT axis
Many more problems than those found by genetic alterations are being detected, which are due to interference on developmental programming of the HPT axis, which set its function at adulthood. The transcriptional regulatory networks that at different stages of development define cellular and circuit phenotypes are being identified [122–124]. Some are relevant for hypothalamic TRHergic neurons [123], but whether they relate to hypophysiotropic PVN neurons is not always known [125, 126]. The development of the components of the HPT axis follows different patterns for which their susceptibility for perturbations extends to various periods. The thyroid gland matures until the second half of pregnancy in humans, and by embryonic (E) day 17.5 in rodents. The fetus depends on mother’s TH delivered through the placenta and the function of the offspring thyroid at birth correlates with that of their mother [127, 128]. Small variations may affect the HPT axis set point [128]. The maturation of neuroendocrine hypothalamus differs between altricial and precocial animals; in rodents it occurs mainly during the postnatal period, whereas in sheep or primates it essentially takes place before birth [129]. However, both pre- and postnatal periods share a sensibility to metabolic and nutritional alterations [129, 130]. Direct effects on the programming of the HPT axis likely depend on time of insult, given the existence of critical periods in the development of the various elements involved.
In rodents, hypothalamic neurogenesis peaks at E12 [PVN: 12–14; ARC: 12–16]; in the rat PVN, TRHergic neuroendocrine neurons are born during the embryonic day 12 [131] and E12.5 in mice [123]. Expression of PVN-Trh increases during lactation as do that of other elements of the HPT axis, such as hypothalamic PPII activity, pituitary TRH receptors, serum concentrations of TSH, TH, and thyroid hormone receptor (Trb1) in the PVN [132–134]. TRH-induced TSH release appears at postnatal day (PND) 5–7 [135, 136]. At birth, D1 is present in liver and pituitary, but T4 to T3 conversion is low in hypothalamus and increases during lactation [137]. In the rat, Dio2 expression is intense at PND 15 in the lateral parts of the median eminence and the lining of the lower portion of the third ventricle [138]. TH feedback effects on Trh mRNA levels in the PVN, TRH-induced TSH release, and pituitary-TSH biosynthesis, are not detected until the 2nd postnatal week, in parallel to increased serum T4 concentrations [139–141]. The mechanisms of the delayed appearance of the feedback control of the HPT axis have been clarified in the chicken, that mature near birth (hatching) as humans do. In this species, the limiting step that explains the time gap between the onset of HPT function and TH-mediated negative feedback is the increase of D2 activity in the hypothalamus (including in the MBH tanycytes). This increase allows a T3 gradient sufficient to establish the set point of the HPT axis, T3 acting on Trb2 whose expression is instituted earlier [142]. Rodent tanycytes appear to differentiate from a subpopulation of radial glia [143, 144]. In the rat, tanycytes are first detected at E18 [145], but most are generated during the first postnatal week. This contrasts with the pattern observed in human hypothalami that express Dio2 since mid-term with almost disappearance around birth and raising again by day 2 [146]. The description of the developmental pattern of D2 activity in rodent tanycytes is lacking but it could permit to test the hypothesis put forward in the chicken.
Another important aspect of the physiology of the hypophysiotropic TRH neurons is the maturation of the connections between ARC and PVN that are formed at PND8–10 [147]. The fetus and newborn have a positive energy balance and leptin is a strong participant in the adequate axonal growth and wiring of these nuclei [129, 147]. Besides leptin, glucocorticoids, insulin and ghrelin control the activity of POMC and NPY/AgRP neurons [129]. Perturbations in the perinatal environment modify the programming of these arcuate neurons, with long-term effects that potentially will affect the activity of PVN-TRH neurons. Some mechanisms involved in the long-lasting effects of early metabolic dysregulations are being elucidated; for example, the reduced adult Pomc gene expression in prenatally over-nourished rats is due to the epigenetic changes (hypermethylation) in the promoter; other epigenetic changes have been identified in the leptin or glucocorticoid receptor genes [130, 147, 148].
The mother’s nutritional status can alter fetal programming and lead to metabolic disturbances in the adult. The hypothalamic cyto-architecture is affected in offspring from malnourished mothers, their offspring showing propensity for obesity and leptin resistance [129]. Small babies at birth, or offspring from malnourished mothers have dysfunctional HPT axis. Protein malnutrition during pregnancy diminishes T3 serum levels and TSH response to cold exposure, possibly because TRH release is inhibited [149, 150]. The opposite situation also has strong deleterious effects on the development of the offspring, as maternal obesity programs it for obesity. In humans, maternal obesity alters the serum concentrations of thyroid hormones and her fT3 serum levels associate with those in the fetus and with the degree of obesity [151]. Multiple models have been studied in an attempt to understand the mechanisms that lead to metabolic programming of obesity [129, 130]. In rodents, offspring from obese mothers have increased number of neurons expressing orexigenic peptides (NPY/AgRP), as well as leptin resistance and altered intra-hypothalamic connectivity [147], changes that may influence development of the HPT axis or its postnatal or adult responses. In post-weaning offspring of HFD-fed rats, the amount of TRH precursor protein is increased in the PVN, together with serum TT3 and fT4 concentrations; white adipose tissue mass and leptin serum concentration are increased together with decreased expression of nuclear factors responsible for transducing leptin signaling in the arcuate (pSTAT3 and SOCS3), suggesting leptin resistance [152]. Overfeeding pups during lactation, from obese mothers, amplifies the hypothalamic changes observed in offspring from obese mothers [153]. In non-human primates under HFD during pregnancy fT4 levels are normal, but their 130 day old fetus do show differences; they have low expression of hypothalamic TRH as well as of genes responsible of thyroid hormone production [154]. In contrast, obese women and their neonate child have altered TH levels [151, 155].
Stress is another very important threat against optimum development. Endogenous glucocorticoids fluctuate during pregnancy; well-timed surges promote the development and maturation of multiple organs including brain, pituitary and thyroid; administration of high concentrations at wrong stages of development may have life-long physiological consequences, such as altered HPA functioning [156]. Stress can also induce hypothyroidism in the mother and in consequence the deficient hormone availability affects brain development of the offspring [127]. Injection of corticosterone to a pregnant rat from E18-E21 decreases core body temperature and Trh mRNA levels in the PVN of female offspring but not males. Although this suggests a gender specific effect, decreased TRH precursor protein amount is detected in PVN fibers of both genders; furthermore, serum T3 concentration diminishes only in males but that of TT4 in both sexes at PND14 while levels are normal by PND60 [157]. The apparent difference in gender response remains to be analyzed under a situation of energy demand, since estrogens have multiple effects on the HPT axis including its response to cold exposure [158], and gender differences in stress response are observed early in life [159].
Since other components of the HPT axis present postnatal maturation, long-lasting alterations may also be provoked by postnatal factors. Postnatal effects are produced by changing the nutritional status. Overfeeding only during lactation by limiting the size of litter, or feeding the mother with HFD, induces obesity in the offspring at adulthood that present several symptoms of hypothyroidism and leptin resistance including low Trh expression in the PVN, and of TSH in the pituitary [153, 160]. Early life stress produces long life changes in metabolism and the stress response of the offspring [161–163]. Based on the initial observations that maternal behaviour predisposes the offspring to these alterations, a model of maternal separation (MS) has been implemented leading to the characterization of the degree of methylation of several stress-responsive genes [162]. Varying degrees of grooming and leaking lead to early changes in circulating T3 and altered hippocampal GR expression which plays a central role in the negative feedback control of the HPA axis [164, 165]. Since the activity of the HPT axis is modulated by acute or chronic stress [1], and because we have shown that stress or corticosterone injections blunt the response of the axis to cold exposure [96], we recently studied the effects of MS on basal and fasting-induced expression of HPT axis activity markers. mRNA levels of PVN-Trh and of PPII in tanycytes were modified by MS in a sex-specific manner. Furthermore, the response to 48 h fasting was partially blunted in MS-males, which could alter their adaptability to energy demanding situations [166].
9 Environmental insults and the HPT axis
It has been recognized for long time that cigarette smoke alters the activity of the HPT axis of the offspring, whether exposed in uterus or afterwards [167]. Recent work contributes to the understanding of the mechanisms involved; nicotine administered to lactating mothers since the 2nd postpartum day causes in the adult offspring increased fat mass and circulating leptin concentration, with symptoms of leptin resistance. In addition, it provokes tertiary hypothyroidism evidenced by low Trh expression in PVN, TSH concentration in pituitary, and altered deiodinase activity in liver and BAT [168].
The multiple dangers imposed by chemicals in the environment have become now evident. Many of them cause endocrine alterations for which they are now recognized as endocrine disruptors. Their degree of toxicity varies depending on whether they coincide with a critical period of development, as they can bind to hormone receptors and thus affect hormone signaling [169, 170]. Recent reviews cover the variety of compounds ranging from cosmetics, insecticides, plastic derivatives, and flame retardants that affect the thyroid axis at different levels including the expression of Trh receptor [171–175], although to our knowledge, data on Trh expression are still lacking.
10 Conclusions
In the last years, there has been a steady increase in the knowledge of the mechanisms involved in TRH signaling and its central role in modulating the HPT axis. Among the new data, we can pin-point the mechanisms that control the transcription of the Trh gene, with the identification of new transcription factors engaged in Trh gene expression, as well as how signaling pathways define the dynamics of TRH-neurons response to acute and/or long-term influences. A better, albeit yet incomplete, description of the response and relationship of TRH neurons activity with positive energy balance has also emerged, as well as putative intermediary mechanisms. The importance of tanycytes as a central relay for the feedback control of the axis, as well as for HPT responses to alterations in energy balance, and other stimuli has been reinforced. Tanycytes seem critical for hypophysiotropic TRH neurons activity, but also to control the extracellular fate of released TRH through the activity of the TRH degrading enzyme. A relationship between polymorphism in the TRH-R gene and lean body mass underlines the critical role of TRH signaling in health. In addition, some studies have started to shed light on the interference of maternal and postnatal stress and nutrition on HPT axis programming, and confirmed the axis susceptibility to early insults, including the devastating effects of endocrine disruptors.
References
Joseph-Bravo P, Jaimes-Hoy L, Charli JL. Regulation of TRH neurons and energy homeostasis-related signals under stress. J Endocrinol. 2015;224(3):R139–59.
Fekete C, Lechan RM. Central regulation of hypothalamic-pituitary-thyroid axis under physiological and pathophysiological conditions. Endocr Rev. 2014;35(2):159–94.
Wittmann G, Füzesi T, Singru PS, Liposits Z, Lechan RM, Fekete C. Efferent projections of thyrotropin-releasing hormone-synthesizing neurons residing in the anterior parvocellular subdivision of the hypothalamic paraventricular nucleus. J Comp Neurol. 2009;515(3):313–30.
Sutton AK, Myers Jr MG, Olson DP. The role of PVH circuits in leptin action and energy balance. Annu Rev Physiol. 2016;78:207–21.
Kalsbeek A, Bruinstroop E, Yi CX, Klieverik LP, La Fleur SE, Fliers E. Hypothalamic control of energy metabolism via the autonomic nervous system. Ann N Y Acad Sci. 2010;1212:114–29.
Shi ZX, Levy A, Lightman SL. Hippocampal input to the hypothalamus inhibits thyrotrophin and thyrotrophin-releasing hormone gene expression. Neuroendocrinology. 1993;57(4):576–80.
Fliers E, Kalsbeek A, Boelen A. Beyond the fixed setpoint of the hypothalamus-pituitary-thyroid axis. Eur J Endocrinol. 2014;171(5):R197–208.
Fliers E, Bianco AC, Langouche L, Boelen A. Thyroid function in critically ill patients. Lancet Diabetes Endocrinol. 2015;3(10):816–25.
Mulcahy LR, Vaslet CA, Nillni EA. Prohormone-convertase 1 processing enhances post-Golgi sorting of prothyrotropin-releasing hormone-derived peptides. J Biol Chem. 2005;280(48):39818–26.
Lochner JE, Kingma M, Kuhn S, Meliza CD, Cutler B, Scalettar BA. Real-time imaging of the axonal transport of granules containing a tissue plasminogen activator/green fluorescent protein hybrid. Mol Biol Cell. 1998;9(9):2463–76.
Goodman T, Hajihosseini MK. Hypothalamic tanycytes-masters and servants of metabolic, neuroendocrine, and neurogenic functions. Front Neurosci. 2015;9:387.
Diano S, Leonard JL, Meli R, Esposito E, Schiavo L. Hypothalamic type II iodothyronine deiodinase: a light and electron microscopic study. Brain Res. 2003;976(1):130–4.
Sánchez E, Vargas MA, Singru PS, Pascual I, Romero F, Fekete C, Charli JL, Lechan RM. Tanycyte pyroglutamyl peptidase II contributes to regulation of the hypothalamic-pituitary-thyroid axis through glial-axonal associations in the median eminence. Endocrinology. 2009;150(5):2283–91.
Charli JL, Cruz C, Vargas MA, Joseph-Bravo P. The narrow specificity pyroglutamate amino peptidase degrading TRH in rat brain is an ectoenzyme. Neurochem Int. 1988;13(2):237–42.
Bauer K, Carmeliet P, Schulz M, Baes M, Denef C. Regulation and cellular localization of the membrane-bound thyrotropin-releasing hormone-degrading enzyme in primary cultures of neuronal, glial and adenohypophyseal cells. Endocrinology. 1990;127(3):1224–33.
Sánchez E, Charli JL, Lechan RM. Pyroglutamyl-peptidase II In: Rawlings, N.D. Handbook of Proteolytic Enzymes. Academic Press. 2013:414–9.
Joseph-Bravo P, Jaimes-Hoy L, Uribe RM, Charli JL. 60 years of neuroendocrinology: TRH, the first hypophysiotropic releasing hormone isolated: control of the pituitary-thyroid axis. J Endocrinol. 2015;226(2):T85–T100.
Galas L, Raoult E, Tonon MC, Okada R, Jenks BG, Castaño JP, Kikuyama S, Malagon M, Roubos EW, Vaudry H. TRH acts as a multifunctional hypophysiotropic factor in vertebrates. Gen Comp Endocrinol. 2009;164(1):40–50.
Hinkle PM, Gehret AU, Jones BW. Desensitization, trafficking, and resensitization of the pituitary thyrotropin-releasing hormone receptor. Front Neurosci. 2012;6:180.
Shupnik MA, Chin WW, Habener JF, Ridgway EC. Transcriptional regulation of the thyrotropin subunit genes by thyroid hormone. J Biol Chem. 1985;260(5):2900–3.
Weintraub BD, Gesundheit N, Taylor T, Gyves PW. Effect of TRH on TSH glycosylation and biological action. Ann N Y Acad Sci. 1989;553:205–13.
Kanasaki H, Oride A, Mijiddorj T, Kyo S. Role of thyrotropin-releasing hormone in prolactin-producing cell models. Neuropeptides. 2015;54:73–7.
Bargi-Souza P, Kucka M, Bjelobaba I, Tomić M, Janjic MM, Nunes MT, Stojilkovic SS. Loss of basal and TRH-stimulated Tshb expression in dispersed pituitary cells. Endocrinology. 2015;156(1):242–54.
Bockmann J, Böckers TM, Winter C, Wittkowski W, Winterhoff H, Deufel T, Kreutz MR. Thyrotropin expression in hypophyseal pars tuberalis-specific cells is 3, 5,3'-triiodothyronine, thyrotropin-releasing hormone, and pit-1 independent. Endocrinology. 1997;138(3):1019–28.
Watanabe T, Yamamura T, Watanabe M, Yasuo S, Nakao N, Dawson A, Ebihara S, Yoshimura T. Hypothalamic expression of thyroid hormone-activating and-inactivating enzyme genes in relation to photorefractoriness in birds and mammals. Am J Physiol Regul Integr Comp Physiol. 2007;292(1):R568–72.
Ono H, Hoshino Y, Yasuo S, Watanabe M, Nakane Y, Murai A, Ebihara S, Korf HW, Yoshimura T. Involvement of thyrotropin in photoperiodic signal transduction in mice. Proc Natl Acad Sci U S A. 2008;105(47):18238–42.
Bolborea M, Helfer G, Ebling FJ, Barrett P. Dual signal transduction pathways activated by TSH receptors in rat primary tanycyte cultures. J Mol Endocrinol. 2015;54(3):241–50.
Ikegami K, Liao XH, Hoshino Y, Ono H, Ota W, Ito Y, Nishiwaki-Ohkawa T, Sato C, Kitajima K, Iigo M, Shigeyoshi Y, Yamada M, Murata Y, Refetoff S, Yoshimura T. Tissue-specific posttranslational modification allows functional targeting of thyrotropin. Cell Rep. 2014;9(3):801–10.
Sugrue ML, Vella KR, Morales C, Lopez ME, Hollenberg AN. The thyrotropin-releasing hormone gene is regulated by thyroid hormone at the level of transcription in vivo. Endocrinology. 2010;151(2):793–801.
Hollenberg AN. The role of the thyrotropin-releasing hormone (TRH) neuron as a metabolic sensor. Thyroid. 2008;18(2):131–9.
Abel ED, Ahima RS, Boers ME, Elmquist JK, Wondisford FE. Critical role for thyroid hormone receptor beta2 in the regulation of paraventricular thyrotropin-releasing hormone neurons. J Clin Invest. 2001;107(8):1017–23.
Ishii S, Yamada M, Satoh T, Monden T, Hashimoto K, Shibusawa N, Onigata K, Morikawa A, Mori M. Aberrant dynamics of histone deacetylation at the thyrotropin-releasing hormone gene in resistance to thyroid hormone. Mol Endocrinol. 2004;18(7):1708–20.
Díaz-Gallardo MY, Cote-Vélez A, Carreón-Rodríguez A, Charli JL, Joseph-Bravo P. Phosphorylated cyclic-AMP-response element-binding protein and thyroid hormone receptor have independent response elements in the rat thyrotropin-releasing hormone promoter: an analysis in hypothalamic cells. Neuroendocrinology. 2010;91(1):64–76.
Vella KR, Ramadoss P, Costa-E-Sousa RH, Astapova I, Ye FD, Holtz KA, Harris JC, Hollenberg AN. Thyroid hormone signaling in vivo requires a balance between coactivators and corepressors. Mol Cell Biol. 2014;34(9):1564–75.
Matsunaga H, Sasaki S, Suzuki S, Matsushita A, Nakamura H, Nakamura HM, Hirahara N, Kuroda G, Iwaki H, Ohba K, Morita H, Oki Y, Suda T. Essential role of GATA2 in the negative regulation of type 2 deiodinase Gene by Liganded thyroid hormone receptor β2 in thyrotroph. PLoS One. 2015;10(11):e0142400.
Mullur R, Liu YY, Brent GA. Thyroid hormone regulation of metabolism. Physiol Rev. 2014;94(2):355–82.
Zhang R, Wang Y, Li R, Chen G. Transcriptional factors mediating retinoic acid signals in the control of energy metabolism. Int J Mol Sci. 2015;16(6):14210–44.
Decherf S, Seugnet I, Becker N, Demeneix BA, Clerget-Froidevaux MS. Retinoic X receptor subtypes exert differential effects on the regulation of Trh transcription. Mol Cell Endocrinol. 2013;381(1–2):115–23.
Sharma V, Hays WR, Wood WM, Pugazhenthi U, St Germain DL, Bianco AC, Krezel W, Chambon P, Haugen BR. Effects of rexinoids on thyrotrope function and the hypothalamic-pituitary-thyroid axis. Endocrinology. 2006;147(3):1438–51.
Stoney PN, Helfer G, Rodrigues D, Morgan PJ, McCaffery P. Thyroid hormone activation of retinoic acid synthesis in hypothalamic tanycytes. Glia. 2016;64(3):425–39.
Kouidhi S, Seugnet I, Decherf S, Guissouma H, Elgaaied AB, Demeneix B, Clerget-Froidevaux MS. Peroxisome proliferator-activated receptor-gamma (PPARgamma) modulates hypothalamic Trh regulation in vivo. Mol Cell Endocrinol. 2010;317(1–2):44–52.
Korach-André M, Gustafsson JÅ. Liver X receptors as regulators of metabolism. Biomol Concepts. 2015;6(3):177–90.
Ghaddab-Zroud R, Seugnet I, Steffensen KR, Demeneix BA, Clerget-Froidevaux MS. Liver X receptor regulation of thyrotropin-releasing hormone transcription in mouse hypothalamus is dependent on thyroid status. PLoS One. 2014;9(9):e106983.
Miao Y, Wu W, Dai Y, Maneix L, Huang B, Warner M, Gustafsson JÅ. Liver X receptor β controls thyroid hormone feedback in the brain and regulates browning of subcutaneous white adipose tissue. Proc Natl Acad Sci U S A. 2015;112(45):14006–11.
Cermenati G, Brioschi E, Abbiati F, Melcangi RC, Caruso D, Mitro N. Liver X receptors, nervous system, and lipid metabolism. J Endocrinol Investig. 2013;36(6):435–43.
Iwen KA, Schröder E, Brabant G. Thyroid hormones and the metabolic syndrome. Eur Thyroid J. 2013;2(2):83–92.
Santini F, Marzullo P, Rotondi M, Ceccarini G, Pagano L, Ippolito S, Chiovato L, Biondi B. Mechanisms in endocrinology: the crosstalk between thyroid gland and adipose tissue: signal integration in health and disease. Eur J Endocrinol. 2014;171(4):R137–52.
Bernal J, Guadaño-Ferraz A, Morte B. Thyroid hormone transporters--functions and clinical implications. Nat Rev Endocrinol. 2015;11(7):406–17.
Schweizer U, Köhrle J. Function of thyroid hormone transporters in the central nervous system. Biochim Biophys Acta. 2013;1830(7):3965–73.
Heuer H, Visser TJ. The pathophysiological consequences of thyroid hormone transporter deficiencies: insights from mouse models. Biochim Biophys Acta. 2013;1830(7):3974–8.
Werneck de Castro JP, Fonseca TL, Ueta CB, McAninch EA, Abdalla S, Wittmann G, Lechan RM, Gereben B, Bianco AC. Differences in hypothalamic type 2 deiodinase ubiquitination explain localized sensitivity to thyroxine. J Clin Invest. 2015;125(2):769–81.
Tu HM, Kim SW, Salvatore D, Bartha T, Legradi G, Larsen PR, Lechan RM. Regional distribution of type 2 thyroxine deiodinase messenger ribonucleic acid in rat hypothalamus and pituitary and its regulation by thyroid hormone. Endocrinology. 1997;138(8):3359–68.
Kalló I, Mohácsik P, Vida B, Zeöld A, Bardóczi Z, Zavacki AM, Farkas E, Kádár A, Hrabovszky E, Arrojo E, Drigo R, Dong L, Barna L, Palkovits M, Borsay BA, Herczeg L, Lechan RM, Bianco AC, Liposits Z, Fekete C, Gereben B. A novel pathway regulates thyroid hormone availability in rat and human hypothalamic neurosecretory neurons. PLoS One. 2012;7(6):e37860.
Tu HM, Legradi G, Bartha T, Salvatore D, Lechan RM, Larsen PR. Regional expression of the type 3 iodothyronine deiodinase messenger ribonucleic acid in the rat central nervous system and its regulation by thyroid hormone. Endocrinology. 1999;140(2):784–90.
Herwig A, Campbell G, Mayer CD, Boelen A, Anderson RA, Ross AW, Mercer JG, Barrett P. A thyroid hormone challenge in hypothyroid rats identifies T3 regulated genes in the hypothalamus and in models with altered energy balance and glucose homeostasis. Thyroid. 2014;24(11):1575–93.
Huang SA, Bianco AC. Reawakened interest in type III iodothyronine deiodinase in critical illness and injury. Nat Clin Pract Endocrinol Metab. 2008;4(3):148–55.
Gereben B, McAninch EA, Ribeiro MO, Bianco AC. Scope and limitations of iodothyronine deiodinases in hypothyroidism. Nat Rev Endocrinol. 2015;11(11):642–52.
Calvino C, Império GE, Wilieman M, Costa-E-Sousa RH, Souza LL, Trevenzoli IH, Pazos-Moura CC. Hypothyroidism induces Hypophagia associated with alterations in protein expression of neuropeptide Y and proopiomelanocortin in the arcuate nucleus, independently of hypothalamic nuclei-specific changes in leptin signaling. Thyroid. 2016;26(1):134–43.
Koller KJ, Wolff RS, Warden MK, Zoeller RT. Thyroid hormones regulate levels of thyrotropin-releasing-hormone mRNA in the paraventricular nucleus. Proc Natl Acad Sci U S A. 1987;84(20):7329–33.
Segerson TP, Kauer J, Wolfe HC, Mobtaker H, Wu P, Jackson IM, Lechan RM. Thyroid hormone regulates TRH biosynthesis in the paraventricular nucleus of the rat hypothalamus. Science. 1987;238(4823):78–80.
Kakucska I, Rand W, Lechan RM. Thyrotropin-releasing hormone gene expression in the hypothalamic paraventricular nucleus is dependent upon feedback regulation by both triiodothyronine and thyroxine. Endocrinology. 1992;130(5):2845–50.
Perello M, Friedman T, Paez-Espinosa V, Shen X, Stuart RC, Nillni EA. Thyroid hormones selectively regulate the posttranslational processing of prothyrotropin-releasing hormone in the paraventricular nucleus of the hypothalamus. Endocrinology. 2006;147(6):2705–16.
Lazcano I, Cabral A, Uribe RM, Jaimes-Hoy L, Perello M, Joseph-Bravo P, Sánchez-Jaramillo E, Charli JL. Fasting enhances pyroglutamyl peptidase II activity in tanycytes of the mediobasal hypothalamus of male adult rats. Endocrinology. 2015;156(7):2713–23.
Marsili A, Sanchez E, Singru P, Harney JW, Zavacki AM, Lechan RM, Larsen PR. Thyroxine-induced expression of pyroglutamyl peptidase II and inhibition of TSH release precedes suppression of TRH mRNA and requires type 2 deiodinase. J Endocrinol. 2011;211(1):73–8.
Bauer K. Regulation of degradation of thyrotropin releasing hormone by thyroid hormones. Nature. 1976;259(5544):591–3.
Schmitmeier S, Thole H, Bader A, Bauer K. Purification and characterization of the thyrotropin-releasing hormone (TRH)-degrading serum enzyme and its identification as a product of liver origin. Eur J Biochem. 2002;269(4):1278–86.
Chiamolera MI, Sidhaye AR, Matsumoto S, He Q, Hashimoto K, Ortiga-Carvalho TM, Wondisford FE. Fundamentally distinct roles of thyroid hormone receptor isoforms in a thyrotroph cell line are due to differential DNA binding. Mol Endocrinol. 2012;26(6):926–39.
Schomburg L, Bauer K. Thyroid hormones rapidly and stringently regulate the messenger RNA levels of the thyrotropin-releasing hormone (TRH) receptor and the TRH-degrading ectoenzyme. Endocrinology. 1995;136(8):3480–5.
Hoermann R, Midgley JE, Larisch R, Dietrich JW. Homeostatic Control of the Thyroid-Pituitary Axis: Perspectives for Diagnosis and Treatment. Front Endocrinol (Lausanne). 2015;6:–177.
Ehrenkranz J, Bach PR, Snow GL, Schneider A, Lee JL, Ilstrup S, Bennett ST, Benvenga S. Circadian and circannual rhythms in thyroid hormones: determining the TSH and free T4 reference intervals based upon time of day, age, and sex. Thyroid. 2015;25(8):954–61.
Cruz R, Chávez-Gutiérrez L, Joseph-Bravo P, Charli JL. 3,3',5'-triiodo-L-thyronine reduces efficiency of mRNA knockdown by antisense oligodeoxynucleotides: a study with pyroglutamyl aminopeptidase II in adenohypophysis. Oligonucleotides. 2004;14(3):176–90.
de Vries EM, Fliers E, Boelen A. The molecular basis of the non-thyroidal illness syndrome. J Endocrinol. 2015;225(3):R67–81.
Sánchez E, Singru PS, Wittmann G, Nouriel SS, Barrett P, Fekete C, Lechan RM. Contribution of TNF-alpha and nuclear factor-kappaB signaling to type 2 iodothyronine deiodinase activation in the mediobasal hypothalamus after lipopolysaccharide administration. Endocrinology. 2010;151(8):3827–35.
Wittmann G, Harney JW, Singru PS, Nouriel SS, Reed Larsen P, Lechan RM. Inflammation-inducible type 2 deiodinase expression in the leptomeninges, choroid plexus, and at brain blood vessels in male rodents. Endocrinology. 2014;155(5):2009–19.
de Vries EM, Kwakkel J, Eggels L, Kalsbeek A, Barrett P, Fliers E, Boelen A. NFκB signaling is essential for the lipopolysaccharide-induced increase of type 2 deiodinase in tanycytes. Endocrinology. 2014;155(5):2000–8.
Wittmann G, Szabon J, Mohácsik P, Nouriel SS, Gereben B, Fekete C, Lechan RM. Parallel regulation of thyroid hormone transporters OATP1c1 and MCT8 during and after endotoxemia at the blood-brain barrier of male rodents. Endocrinology. 2015;156(4):1552–64.
Guo F, Bakal K, Minokoshi Y, Hollenberg AN. Leptin signaling targets the thyrotropin-releasing hormone gene promoter in vivo. Endocrinology. 2004;145(5):2221–7.
Ghamari-Langroudi M, Srisai D, Cone RD. Multinodal regulation of the arcuate/paraventricular nucleus circuit by leptin. Proc Natl Acad Sci U S A. 2011;108(1):355–60.
Légrádi G, Emerson CH, Ahima RS, Flier JS, Lechan RM. Leptin prevents fasting-induced suppression of prothyrotropin-releasing hormone messenger ribonucleic acid in neurons of the hypothalamic paraventricular nucleus. Endocrinology. 1997;138(6):2569–76.
Coppola A, Meli R, Diano S. Inverse shift in circulating corticosterone and leptin levels elevates hypothalamic deiodinase type 2 in fasted rats. Endocrinology. 2005;146(6):2827–33.
Bergen HT, Mizuno T, Taylor J, Mobbs CV. Resistance to diet-induced obesity is associated with increased proopiomelanocortin mRNA and decreased neuropeptide Y mRNA in the hypothalamus. Brain Res. 1999;851(1–2):198–203.
Perello M, Cakir I, Cyr NE, Romero A, Stuart RC, Chiappini F, Hollenberg AN, Nillni EA. Maintenance of the thyroid axis during diet-induced obesity in rodents is controlled at the central level. Am J Physiol Endocrinol Metab. 2010;299(6):E976–89.
Cyr NE, Steger JS, Toorie AM, Yang JZ, Stuart R, Nillni EA. Central Sirt1 regulates body weight and energy expenditure along with the POMC-derived peptide α-MSH and the processing enzyme CPE production in diet-induced obese male rats. Endocrinology. 2015;156(3):961–74.
Cifani C, Micioni Di Bonaventura MV, Pucci M, Giusepponi ME, Romano A, Di Francesco A, Maccarrone M, D'Addario C. Regulation of hypothalamic neuropeptides gene expression in diet induced obesity resistant rats: possible targets for obesity prediction? Front Neurosci. 2015;9:187.
Xia SF, Duan XM, Hao LY, Li LT, Cheng XR, Xie ZX, Qiao Y, Li LR, Tang X, Shi YH, Le GW. Role of thyroid hormone homeostasis in obesity-prone and obesity-resistant mice fed a high-fat diet. Metabolism. 2015;64(5):566–79.
Byerly MS, Simon J, Lebihan-Duval E, Duclos MJ, Cogburn LA, Porter TE. Effects of BDNF, T3, and corticosterone on expression of the hypothalamic obesity gene network in vivo and in vitro. Am J Physiol Regul Integr Comp Physiol. 2009;296(4):R1180–9.
Cao L, Choi EY, Liu X, Martin A, Wang C, Xu X, During MJ. White to brown fat phenotypic switch induced by genetic and environmental activation of a hypothalamic-adipocyte axis. Cell Metab. 2011;14(3):324–38.
Mariman EC, Bouwman FG, Aller EE, van Baak MA, Wang P. Extreme obesity is associated with variation in genes related to the circadian rhythm of food intake and hypothalamic signaling. Physiol Genomics. 2015;47(6):225–31.
Nuzzaci D, Laderrière A, Lemoine A, Nédélec E, Pénicaud L, Rigault C, Benani A. Plasticity of the Melanocortin System: Determinants and Possible Consequences on Food Intake. Front Endocrinol (Lausanne). 2015;6:–143.
Waterson MJ, Horvath TL. Neuronal regulation of energy homeostasis: beyond the hypothalamus and feeding. Cell Metab. 2015;22(6):962–70.
Uribe RM, Redondo JL, Charli JL, Joseph-Bravo P. Suckling and cold stress rapidly and transiently increase TRH mRNA in the paraventricular nucleus. Neuroendocrinology. 1993;58(1):140–5.
Gutiérrez-Mariscal M, Sánchez E, García-Vázquez A, Rebolledo-Solleiro D, Charli JL, Joseph-Bravo P. Acute response of hypophysiotropic thyrotropin releasing hormone neurons and thyrotropin release to behavioral paradigms producing varying intensities of stress and physical activity. Regul Pept. 2012;179(1–3):61–70.
Sánchez E, Uribe RM, Corkidi G, Zoeller RT, Cisneros M, Zacarias M, Morales-Chapa C, Charli JL, Joseph-Bravo P. Differential responses of thyrotropin-releasing hormone (TRH) neurons to cold exposure or suckling indicate functional heterogeneity of the TRH system in the paraventricular nucleus of the rat hypothalamus. Neuroendocrinology. 2001;74(6):407–22.
Aguilar-Valles A, Sánchez E, de Gortari P, García-Vazquez AI, Ramírez-Amaya V, Bermúdez-Rattoni F, Joseph-Bravo P. The expression of TRH, its receptors and degrading enzyme is differentially modulated in the rat limbic system during training in the Morris water maze. Neurochem Int. 2007;50(2):404–17.
Perello M, Stuart RC, Vaslet CA, Nillni EA. Cold exposure increases the biosynthesis and proteolytic processing of prothyrotropin-releasing hormone in the hypothalamic paraventricular nucleus via beta-adrenoreceptors. Endocrinology. 2007;148(10):4952–64.
Sotelo-Rivera I, Jaimes-Hoy L, Cote-Vélez A, Espinoza-Ayala C, Charli JL, Joseph-Bravo P. An acute injection of corticosterone increases thyrotrophin-releasing hormone expression in the paraventricular nucleus of the hypothalamus but interferes with the rapid hypothalamus pituitary thyroid axis response to cold in male rats. J Neuroendocrinol. 2014;26(12):861–9.
McAninch EA, Bianco AC. Thyroid hormone signaling in energy homeostasis and energy metabolism. Ann N Y Acad Sci. 2014;1311:77–87.
Zoeller RT, Kabeer N, Albers HE. Cold exposure elevates cellular levels of messenger ribonucleic acid encoding thyrotropin-releasing hormone in paraventricular nucleus despite elevated levels of thyroid hormones. Endocrinology. 1990;127(6):2955–62.
Cote-Vélez A, Pérez-Martínez L, Díaz-Gallardo MY, Pérez-Monter C, Carreón-Rodríguez A, Charli JL, Joseph-Bravo P. Dexamethasone represses cAMP rapid upregulation of TRH gene transcription: identification of a composite glucocorticoid response element and a cAMP response element in TRH promoter. J Mol Endocrinol. 2005;34(1):177–97.
Cote-Vélez A, Pérez-Martínez L, Charli JL, Joseph-Bravo P. The PKC and ERK/MAPK pathways regulate glucocorticoid action on TRH transcription. Neurochem Res. 2008;33(8):1582–91.
Díaz-Gallardo MY, Cote-Vélez A, Charli JL, Joseph-Bravo P. A rapid interference between glucocorticoids and cAMP-activated signalling in hypothalamic neurons prevents binding of phosphorylated cAMP response element binding protein and glucocorticoid receptor at the CRE-like and composite GRE sites of thyrotrophin-releasing hormone gene promoter. J Neuroendocrinol. 2010;22(4):282–93.
Cote-Vélez A, Pérez-Maldonado A, Osuna J, Barrera B, Charli JL, Joseph-Bravo P. Creb and Sp/Krüppel response elements cooperate to control rat TRH gene transcription in response to cAMP. Biochim Biophys Acta. 2011;1809(3):191–9.
Sarkar S, Légrádi G, Lechan RM. Intracerebroventricular administration of alpha-melanocyte stimulating hormone increases phosphorylation of CREB in TRH- and CRH-producing neurons of the hypothalamic paraventricular nucleus. Brain Res. 2002;945(1):50–9.
Osterlund C, Spencer RL. Corticosterone pretreatment suppresses stress-induced hypothalamic-pituitary-adrenal axis activity via multiple actions that vary with time, site of action, and de novo protein synthesis. J Endocrinol. 2011;208(3):311–22.
Knoedler JR, Denver RJ. Krüppel-like factors are effectors of nuclear receptor signaling. Gen Comp Endocrinol. 2014;203:49–59.
Mastorakos G, Pavlatou M. Exercise as a stress model and the interplay between the hypothalamus-pituitary-adrenal and the hypothalamus-pituitary-thyroid axes. Horm Metab Res. 2005;37(9):577–84.
Fortunato RS, Ignácio DL, Padron AS, Peçanha R, Marassi MP, Rosenthal D, Werneck-de-Castro JP, Carvalho DP. The effect of acute exercise session on thyroid hormone economy in rats. J Endocrinol. 2008;198(2):347–53.
Ignacio DL, da S Silvestre DH, Cavalcanti-de-Albuquerque JP, Louzada RA, Carvalho DP, Werneck-de-Castro JP. Thyroid hormone and estrogen regulate exercise-induced growth hormone release. PLoS One. 2015;10(4):e0122556.
Uribe RM, Jaimes-Hoy L, Ramírez-Martínez C, García-Vázquez A, Romero F, Cisneros M, Cote-Vélez A, Charli JL, Joseph-Bravo P. Voluntary exercise adapts the hypothalamus-pituitary-thyroid axis in male rats. Endocrinology. 2014;155(5):2020–30.
Martin B, Ji S, Maudsley S, Mattson MP. “control” laboratory rodents are metabolically morbid: why it matters. Proc Natl Acad Sci U S A. 2010;107(14):6127–33.
Yamada M, Satoh T, Mori M. Mice lacking the thyrotropin-releasing hormone gene: what do they tell us? Thyroid. 2003;13(12):1111–21.
García M, Fernández A, Moreno JC. Central hypothyroidism in children. Endocr Dev. 2014;26:79–107.
Medici M, Visser WE, Visser TJ, Peeters RP. Genetic determination of the hypothalamic-pituitary-thyroid axis: where do we stand? Endocr Rev. 2015;36(2):214–44.
Schoenmakers N, Alatzoglou KS, Chatterjee VK, Dattani MT. Recent advances in central congenital hypothyroidism. J Endocrinol. 2015;227(3):R51–71.
Koulouri O, Nicholas AK, Schoenmakers E, Mokrosinski J, Lane F, Cole T, Kirk J, Farooqi IS, Chatterjee VK, Gurnell M, Schoenmakers N. A novel thyrotropin-releasing hormone receptor missense mutation (P81R) in central congenital hypothyroidism. J Clin Endocrinol Metab. 2016;101(3):847–51.
Collu R, Tang J, Castagné J, Lagacé G, Masson N, Huot C, Deal C, Delvin E, Faccenda E, Eidne KA, Van Vliet G. A novel mechanism for isolated central hypothyroidism: inactivating mutations in the thyrotropin-releasing hormone receptor gene. J Clin Endocrinol Metab. 1997;82(5):1561–5.
Bonomi M, Busnelli M, Beck-Peccoz P, Costanzo D, Antonica F, Dolci C, Pilotta A, Buzi F, Persani L. A family with complete resistance to thyrotropin-releasing hormone. N Engl J Med. 2009;360(7):731–4.
Rabeler R, Mittag J, Geffers L, Rüther U, Leitges M, Parlow AF, Visser TJ, Bauer K. Generation of thyrotropin-releasing hormone receptor 1-deficient mice as an animal model of central hypothyroidism. Mol Endocrinol. 2004;18(6):1450–60.
Fuku N, He ZH, Sanchis-Gomar F, Pareja-Galeano H, Tian Y, Arai Y, Abe Y, Murakami H, Miyachi M, Zempo H, Naito H, Yvert T, Verde Z, Venturini L, Fiuza-Luces C, Santos-Lozano A, Rodriguez-Romo G, Ricevuti G, Hirose N, Emanuele E, Garatachea N, Lucia A. Exceptional longevity and muscle and fitness related genotypes: a functional in vitro analysis and case-control association replication study with SNPs THRH rs7832552, IL6 rs1800795, and ACSL1 rs6552828. Front Aging Neurosci. 2015;7:59.
Liu XG, Tan LJ, Lei SF, Liu YJ, Shen H, Wang L, Yan H, Guo YF, Xiong DH, Chen XD, Pan F, Yang TL, Zhang YP, Guo Y, Tang NL, Zhu XZ, Deng HY, Levy S, Recker RR, Papasian CJ, Deng HW. Genome-wide association and replication studies identified TRHR as an important gene for lean body mass. Am J Hum Genet. 2009;84(3):418–23.
Lunardi CC, Lima RM, Pereira RW, Leite TK, Siqueira AB, Oliveira RJ. Association between polymorphisms in the TRHR gene, fat-free mass, and muscle strength in older women. Age (Dordr). 2013;35(6):2477–83.
Shimogori T, Lee DA, Miranda-Angulo A, Yang Y, Wang H, Jiang L, Yoshida AC, Kataoka A, Mashiko H, Avetisyan M, Qi L, Qian J, Blackshaw S. A genomic atlas of mouse hypothalamic development. Nat Neurosci. 2010;13(6):767–75.
Díaz C, Morales-Delgado N, Puelles L. Ontogenesis of peptidergic neurons within the genoarchitectonic map of the mouse hypothalamus. Front Neuroanat. 2014;8:162.
Pearson CA, Placzek M. Development of the medial hypothalamus: forming a functional hypothalamic-neurohypophyseal interface. Curr Top Dev Biol. 2013;106:49–88.
Guerra-Crespo M, Pérez-Monter C, Janga SC, Castillo-Ramírez S, Gutiérrez-Rios RM, Joseph-Bravo P, Pérez-Martínez L, Charli JL. Transcriptional profiling of fetal hypothalamic TRH neurons. BMC Genomics. 2011;12:222.
Martínez-Armenta M. Díaz de León-Guerrero S, Catalán a, Alvarez-Arellano L, Uribe RM, Subramaniam M, Charli JL, Pérez-Martínez L. TGFβ2 regulates hypothalamic Trh expression through the TGFβ inducible early gene-1 (TIEG1) during fetal development. Mol Cell Endocrinol. 2015;400:129–39.
Moog NK, Entringer S, Heim C, Wadhwa PD, Kathmann N, Buss C. Influence of maternal thyroid hormones during gestation on fetal brain development. Neuroscience (2015). doi:10.1016/j.neuroscience.2015.09.070.
Korevaar TI, Chaker L, Jaddoe VW, Visser TJ, Medici M, Peeters RP. Maternal and birth characteristics are determinants of offspring thyroid function. J Clin Endocrinol Metab. 2016;101(1):206–13.
Gali Ramamoorthy T, Begum G, Harno E, White A. Developmental programming of hypothalamic neuronal circuits: impact on energy balance control. Front Neurosci. 2015;9:126.
Lecoutre S, Breton C. Maternal nutritional manipulations program adipose tissue dysfunction in offspring. Front Physiol. 2015;6:158.
Markakis EA, Swanson LW. Spatiotemporal patterns of secretomotor neuron generation in the parvicellular neuroendocrine system. Brain Res Brain Res Rev. 1997;24(2–3):255–91.
Bradley DJ, Towle HC, Young WS, 3rd Spatial and temporal expression of alpha- and beta-thyroid hormone receptor mRNAs, including the beta 2-subtype, in the developing mammalian nervous system. J Neurosci 1992; 12(6):2288–2302.
Burgunder JM, Taylor T. Ontogeny of thyrotropin-releasing hormone gene expression in the rat diencephalon. Neuroendocrinology. 1989;49(6):631–40.
Vargas MA, Herrera J, Uribe RM, Charli JL, Joseph-Bravo P. Ontogenesis of pyroglutamyl peptidase II activity in rat brain, adenohypophysis and pancreas. Brain Res Dev Brain Res. 1992;66(2):251–6.
Oliver C, Giraud P, Lissitzky JC, Contye-Devolx B, Gillioz P. Influence of thyrotropin-releasing hormone on the secretion of thyrotropin in neonatal rats. Endocrinology. 1981;108(1):179–82.
Strbak V, Greer MA. Thyrotropin secretory response to thyrotropin-releasing hormone in the hypothyroid perinatal rat: further evidence of thyrotrophs independence of the hypothalamus during early ontogenesis. Endocrinology. 1981;108(4):1403–6.
Kaplan MM, Yaskoski KA. Maturational patterns of iodothyronine phenolic and tyrosyl ring deiodinase activities in rat cerebrum, cerebellum, and hypothalamus. J Clin Invest. 1981;67(4):1208–14.
Guadaño-Ferraz A, Obregón MJ, St Germain DL, Bernal J. The type 2 iodothyronine deiodinase is expressed primarily in glial cells in the neonatal rat brain. Proc Natl Acad Sci U S A. 1997;94(19):10391–6.
Rodríguez-García M, Jolín T, Santos A, Pérez-Castillo A. Effect of perinatal hypothyroidism on the developmental regulation of rat pituitary growth hormone and thyrotropin genes. Endocrinology. 1995;136(10):4339–50.
Taylor T, Gyves P, Burgunder JM. Thyroid hormone regulation of TRH mRNA levels in rat paraventricular nucleus of the hypothalamus changes during ontogeny. Neuroendocrinology. 1990;52(3):262–7.
Walker P, Coulombe P, Dussault JH. Effects of triiodothyronine on thyrotropin-releasing hormone-induced thyrotropin release in the neonatal rat. Endocrinology. 1980;107(6):1731–7.
Mohácsik P, Füzesi T, Doleschall M, Szilvásy-Szabó A, Vancamp P, Hadadi É, Darras VM, Fekete C, Gereben B. Increased thyroid hormone activation accompanies the formation of thyroid hormone-dependent negative feedback in developing chicken hypothalamus. Endocrinology. 2016;157(3):1211–21.
Maggi R, Zasso J, Conti L. Neurodevelopmental origin and adult neurogenesis of the neuroendocrine hypothalamus. Front Cell Neurosci. 2015;8:440.
Rützel H, Schiebler TH. Prenatal and early postnatal development of the glial cells in the median eminence of the rat. Cell Tissue Res. 1980;211(1):117–37.
Altman J, Bayer SA. Development of the diencephalon in the rat. III. Ontogeny of the specialized ventricular linings of the hypothalamic third ventricle. J Comp Neurol. 1978;182(4 Pt 2):995–1015.
Alkemade A. Thyroid hormone and the developing hypothalamus. Front Neuroanat. 2015;9:15.
Dearden L, Ozanne SE. Early life origins of metabolic disease: developmental programming of hypothalamic pathways controlling energy homeostasis. Front Neuroendocrinol. 2015;39:3–16.
Ralevski A, Horvath TL. Developmental programming of hypothalamic neuroendocrine systems. Front Neuroendocrinol. 2015;39:52–8.
Aláez C, Calvo R, Obregón MJ, Pascual-Leone AM. Thyroid hormones and 5'-deiodinase activity in neonatal undernourished rats. Endocrinology. 1992;130(2):773–9.
Ayala-Moreno R, Racotta R, Anguiano B, Aceves C, Quevedo L. Perinatal undernutrition programmes thyroid function in the adult rat offspring. Br J Nutr. 2013;110(12):2207–15.
Kahr MK, Antony KM, DelBeccaro M, Hu M, Aagaard KM, Suter MA. Increasing maternal obesity is associated with alterations in both maternal and neonatal thyroid hormone levels. Clin Endocrinol. 2016;84(4):551–7.
Franco JG, Fernandes TP, Rocha CP, Calviño C, Pazos-Moura CC, Lisboa PC, Moura EG, Trevenzoli IH. Maternal high-fat diet induces obesity and adrenal and thyroid dysfunction in male rat offspring at weaning. J Physiol. 2012;590(21):5503–18.
Lisboa PC, Conceição EP, de Oliveira E, Moura EG. Postnatal overnutrition programs the thyroid hormone metabolism and function in adulthood. J Endocrinol. 2015;226(3):219–26.
Suter MA, Sangi-Haghpeykar H, Showalter L, Shope C, Hu M, Brown K, Williams S, Harris RA, Grove KL, Lane RH, Aagaard KM. Maternal high-fat diet modulates the fetal thyroid axis and thyroid gene expression in a nonhuman primate model. Mol Endocrinol. 2012;26(12):2071–80.
Saben J, Kang P, Zhong Y, Thakali KM, Gomez-Acevedo H, Borengasser SJ, Andres A, Badger TM, Shankar K. RNA-seq analysis of the rat placentation site reveals maternal obesity-associated changes in placental and offspring thyroid hormone signaling. Placenta. 2014;35(12):1013–20.
Moisiadis VG, Matthews SG. Glucocorticoids and fetal programming part 1: outcomes. Nat Rev Endocrinol. 2014;10(7):391–402.
Carbone DL, Zuloaga DG, Lacagnina AF, McGivern RF, Handa RJ. Exposure to dexamethasone during late gestation causes female-specific decreases in core body temperature and prepro-thyrotropin-releasing hormone expression in the paraventricular nucleus of the hypothalamus in rats. Physiol Behav. 2012;108:6–12.
Uribe RM, Zacarias M, Corkidi G, Cisneros M, Charli JL, Joseph-Bravo P. 17β-Oestradiol indirectly inhibits thyrotrophin-releasing hormone expression in the hypothalamic paraventricular nucleus of female rats and blunts thyroid axis response to cold exposure. J Neuroendocrinol. 2009;21(5):439–48.
Panagiotakopoulos L, Neigh GN. Development of the HPA axis: where and when do sex differences manifest? Front Neuroendocrinol. 2014;35(3):285–302.
Aréchiga-Ceballos F, Alvarez-Salas E, Matamoros-Trejo G, Amaya MI, García-Luna C, de Gortari P. Pro-TRH and pro-CRF expression in paraventricular nucleus of small litter-reared fasted adult rats. J Endocrinol. 2014;221(1):77–88.
Maccari S, Krugers HJ, Morley-Fletcher S, Szyf M, Brunton PJ. The consequences of early-life adversity: neurobiological, behavioural and epigenetic adaptations. J Neuroendocrinol. 2014;26(10):707–23.
Turecki G, Meaney MJ. Effects of the social environment and stress on glucocorticoid receptor Gene methylation: a systematic review. Biol Psychiatry. 2016;79(2):87–96.
Maniam J, Antoniadis C, Morris MJ. Early-Life Stress, HPA Axis Adaptation, and Mechanisms Contributing to Later Health Outcomes. Front Endocrinol (Lausanne). 2014;5:–73.
Meaney MJ, Diorio J, Francis D, Weaver S, Yau J, Chapman K, Seckl JR. Postnatal handling increases the expression of cAMP-inducible transcription factors in the rat hippocampus: the effects of thyroid hormones and serotonin. J Neurosci. 2000;20(10):3926–35.
Hellstrom IC, Dhir SK, Diorio JC, Meaney MJ. Maternal licking regulates hippocampal glucocorticoid receptor transcription through a thyroid hormone-serotonin-NGFI-A signalling cascade. Philos Trans R Soc Lond Ser B Biol Sci. 2012;367(1601):2495–510.
Jaimes-Hoy L, Gutiérrez-Mariscal M, Vargas Y, Pérez-Maldonado A, Romero F, Sánchez-Jaramillo E, Charli J-L, Joseph-Bravo P. Neonatal maternal separation alters, in a sex specific manner, the expression of TRH, of TRH-degrading ectoenzyme in the rat hypothalamus, and the response of the thyroid axis to starvation. Endocrinology. 2016;157:32–53.
Leach PT, Gould TJ. Thyroid hormone signaling: contribution to neural function, cognition, and relationship to nicotine. Neurosci Biobehav Rev. 2015;57:252–63.
Lisboa PC, de Oliveira E, Manhães AC, Santos-Silva AP, Pinheiro CR, Younes-Rapozo V, Faustino LC, Ortiga-Carvalho TM, Moura EG. Effects of maternal nicotine exposure on thyroid hormone metabolism and function in adult rat progeny. J Endocrinol. 2015;224(3):315–25.
Kabir ER, Rahman MS, Rahman I. A review on endocrine disruptors and their possible impacts on human health. Environ Toxicol Pharmacol. 2015;40(1):241–58.
Dishaw LV, Macaulay LJ, Roberts SC, Stapleton HM. Exposures, mechanisms, and impacts of endocrine-active flame retardants. Curr Opin Pharmacol. 2014;19:125–33.
Préau L, Fini JB, Morvan-Dubois G, Demeneix B. Thyroid hormone signaling during early neurogenesis and its significance as a vulnerable window for endocrine disruption. Biochim Biophys Acta. 2015;1849(2):112–21.
Duntas LH. Chemical contamination and the thyroid. Endocrine. 2015;48(1):53–64.
Duntas LH, Stathatos N. Toxic chemicals and thyroid function: hard facts and lateral thinking. Rev Endocr Metab Disord 2016 Jan 23. [Epub ahead of print] PubMed
Zoeller TR. Environmental chemicals targeting thyroid. Hormones (Athens). 2010;9(1):28–40.
Vuong AM, Webster GM, Romano ME, Braun JM, Zoeller RT, Hoofnagle AN, Sjödin A, Yolton K, Lanphear BP, Chen A. Maternal Polybrominated diphenyl ether (PBDE) exposure and thyroid hormones in maternal and cord sera: the HOME study, Cincinnati. USA Environ Health Perspect. 2015;123(10):1079–85.
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-Dirección General de Asuntos del Personal Académico-Universidad Nacional Autónoma de México, # IA201515 (LJH), # IN204316 (PJB), # IN208515 (JLC).
-Consejo Nacional de Ciencia y Tecnología, Mexico, #CB-180009 (PJB), # CB-154931 (JLC), # CB-254960 (JLC).
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Joseph-Bravo, P., Jaimes-Hoy, L. & Charli, JL. Advances in TRH signaling. Rev Endocr Metab Disord 17, 545–558 (2016). https://doi.org/10.1007/s11154-016-9375-y
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DOI: https://doi.org/10.1007/s11154-016-9375-y