Abstract
Aims/hypothesis
In humans, glucagon-like peptide-1 (GLP-1) is rapidly degraded by dipeptidyl peptidase-4 to a relatively stable metabolite, GLP-1(9–36)NH2, which allows measurement of GLP-1 secretion. However, little is known about the kinetics of the GLP-1 metabolite in mice. We hypothesised that the GLP-1 metabolite is rapidly degraded in this species by neutral endopeptidase(s) (NEP[s]).
Methods
We administered glucose, mixed meal or water orally to 256 mice, and took blood samples before and 2, 6, 10, 20, 30, 60 or 90 min after stimulation. To study the metabolism of the GLP-1 metabolite, i.v. GLP-1(9–36)NH2 (800 fmol) or saline (154 mmol/l NaCl) was administered to 160 mice, some of which had a prior injection of a selective NEP 24.11 ± inhibitor (candoxatril, 5 mg/kg) or saline. Blood was collected before and 1, 2, 4 and 12 min after GLP-1/saline injection. Plasma GLP-1 levels were analysed using a customised single-site C-terminal ELISA, two different two-site ELISAs and MS.
Results
GLP-1 secretion profiles after oral glucose administration differed markedly when assayed by C-terminal ELISA compared with sandwich ELISAs, with the former showing a far higher peak value and AUC. In mice injected with GLP-1(9–36)NH2, immunoreactive GLP-1 plasma levels peaked at approximately 75 pmol/l at 1 min when measured with sandwich ELISAs, returning to baseline (~20 pmol/l) after 12 min, but remained elevated using the C-terminal ELISA (~90 pmol/l at 12 min). NEP 24.11 inhibition by candoxatril significantly attenuated GLP-1(9–36)NH2 degradation in vivo and in vitro. MS identified GLP-1 fragments consistent with NEP 24.11 degradation.
Conclusions/interpretation
In mice, the GLP-1 metabolite is eliminated within a few minutes owing to endoproteolytic cleavage by NEP 24.11. Therefore, accurate measurement of GLP-1 secretion in mice requires assays for NEP 24.11 metabolites. Conventional sandwich ELISAs are inadequate because of endoproteolytic cleavage of the dipeptidyl peptidase-4-generated metabolite.
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Introduction
The incretin hormone glucagon-like peptide-1 (GLP-1) is secreted from enteroendocrine L cells of the gastrointestinal mucosa [1] in response to several nutrients [2, 3]. When intact GLP-1(7–36)NH2 (also termed active GLP-1) enters the capillaries of the small intestine, it is rapidly degraded N-terminally by the enzyme dipeptidyl peptidase-4 (DPP-4) to form the metabolite GLP-1(9–36)NH2, which is devoid of insulinotropic activity [4,5,6]. Consequently, only a minor fraction (~8%) of secreted GLP-1 reaches the target organs in its intact form [7]. Inhibition of DPP-4 causes levels of circulating intact GLP-1(7–36)NH2 to increase several fold; therefore, DPP-4 inhibitors are used as glucose-lowering agents in individuals with type 2 diabetes [8]. Because of the rapid degradation, circulating levels of the intact hormone are often below the detection limit of assays. Assays reacting with the amidated C-terminal, however, will measure both the intact hormone and the metabolite (‘total GLP-1’) and are therefore used to estimate secretion of GLP-1 in humans (Fig. 1) [9]. However, GLP-1 degradation may also involve endoproteolytic mechanism(s) (e.g. catalysis by neutral endopeptidase [NEP] 24.11) [10,11,12]. In mice, measurements of total GLP-1 secretion have given inconsistent results, with most stimuli resulting in insignificant changes [13,14,15,16,17,18,19]. The stability of the primary GLP-1 metabolite, (9–36)NH2, which forms the basis for the common ‘total GLP-1 assays’, is unknown in mice, primarily owing to a lack of adequate immuno-based quantification technologies (assays). As a result, relatively little is known about GLP-1 secretion in mice.
We investigated the secretory profile of GLP-1 and its primary metabolite in mice using an array of biochemical techniques, including a novel customised bead-based fluorescent assay and a highly sensitive MS-based platform [20].
Methods
Animal studies
Mice
All animal experiments were approved by the Danish National Committee for Animal Studies, Ministry of Justice (2013-15-2934-00833), and were performed in accordance with EU Directive 2010/63/EU, Danish legislation governing animal experimentation (1987) and guidelines from the National Institutes of Health (publication number 85-23). Female and male C57BL/6JRj mice, aged 10–12 weeks, were obtained from Janvier Labs (Saint-Berthevin, France). Mice were housed in groups of six to eight in individually ventilated cages, with a 12 h light cycle (lights on 06:00–18:00) and ad libitum access to standard chow (Altromin Spezialfutter, Lage, Germany) and water. To minimise stress on the day of the experiment, the mice were weighed and tail-marked the day before.
Orally stimulated GLP-1 secretion in conscious mice
Female mice (n = 256) were fasted for 6 h (8:00–14:00) with free access to water. At time 0, the animals were orally gavaged with 0.004 ml/g body weight of: (1) d-glucose, 2 g/kg body weight, 50% wt/vol. (Sigma-Aldrich, St Louis, MO, USA); (2) mixed meal NAN2 Pro mixture (Nestlé, Vevey, France); or (3) tap water. A maximal single blood sample (~400 μl) was obtained via a facial vein at 0, 2, 6, 10, 20, 30, 60 or 90 min after oral gavage (n = 6–10 per time point per group), after which the animals were euthanised. Animals designated for sampling at time 0 min did not receive any oral gavage. Blood glucose was measured directly after collection using a handheld glucometer (Accu-Chek Compact Plus; F. Hoffmann–La Roche, Basel, Switzerland). Blood was transferred into pre-chilled EDTA-coated tubes (Microvette 500 K3E; Sarstedt, Nümbrecht, Germany) and centrifuged (1650 g, 4°C, 15 min). Plasma was transferred to Eppendorf tubes and immediately frozen on dry ice according to optimised sample handling procedures [21]. Data for mixed meal are shown in electronic supplementary material (ESM) Fig. 1.
Gastrointestinal biopsies
Female mice (n = 6) were anaesthetised by i.p. injection with a mixture of ketamine (90 mg/kg; Ketaminol Vet.; MSD Animal Health, Madison, NJ, USA) and xylazine (10 mg/kg; Rompun Vet.; Bayer Animal Health, Leverkusen, Germany). The small intestine and stomach were harvested and thoroughly rinsed in cold PBS, and 1 cm samples were snap frozen on dry ice and stored at −80°C until protein extraction, as described previously [22]. Extracts were purified using pH-resistant tC18 cartridges (Waters, Hedehusene, Denmark), dried under a gentle stream of compressed air overnight and reconstituted in 1 ml of TRIS buffer (100 mmol/l TRIS buffer [Sigma-Aldrich] supplemented with 0.1% [wt/vol.] human serum albumin [Merck, Darmstadt, Germany], 20 mmol/l EDTA and 0.6 mmol/l thimerosal [Sigma Chemical Co., St Louis, MO, USA]; pH 8.5), and further diluted in assay buffer to ensure that the measured concentrations were within the sensitive ranges of the respective assays.
Perfused upper small intestine
Male mice (n = 6) were anaesthetised as described above, and the upper small intestine was isolated and perfused as previously described [23].
Injection of GLP-1(9–36)NH2
Female mice (n = 160) were anaesthetised with isoflurane (Baxter, Lillerod, Denmark; flow concentration: 1.5% [vol./vol.]). Candoxatril (a selective NEP 24.11 inhibitor [24, 25]; 5 mg/kg, dissolved in 0.9% NaCl, provided by J. Lundbeck, Novo Nordisk, Måløv, Denmark) or saline (154 mmol/l NaCl) was administered as an i.v. bolus injection into the vena cava through an insulin needle 2 min before injection of GLP-1. At time 0, either 800 fmol GLP-1(9–36)NH2 (see below) or saline was administered through the inferior vena cava (injection volume 100 μl). A maximal blood sample (~400 μl) was drawn from the inferior vena cava at 0, 1, 2, 4, 8 or 12 min after injection (n = 4–8 per time point), after which the animals were euthanised. Blood was immediately transferred into pre-chilled EDTA-coated microtest tubes (VWR, Søborg, Denmark). Animals designated for sampling at time 0 min did not receive any i.v. injection. Blood glucose was measured immediately, as described above. Blood was centrifuged and handled as described above.
In vitro degradation of GLP-1(9–36)NH2
Heparinised mouse plasma was obtained from Equitech-Bio (Kerrville, TX, USA). In addition, EDTA plasma was obtained as follows: female mice (n = 38) were anaesthetised with isoflurane, and blood was drawn from the inferior vena cava, pooled into 6 ml EDTA-coated tubes (VWR) and centrifuged (1650 g, 4°C, 15 min). Plasma was separated immediately and kept chilled. Synthetic GLP-1(9–36)NH2 (see below) was added to each plasma pool (final concentration 200 pmol). Each pool was then divided into four equal portions, to which was added 10 μl of: (1) saline; (2) DPP-4 inhibitor (valine pyrrolidide, a gift from Novo Nordisk, Denmark; final concentration 0.01 mmol/l); (3) NEP 24.11 inhibitor (phosphoramidon; Sigma-Aldrich, Brøndby, Denmark; final concentration 3.5 μmol/l); or (4) an inhibitor cocktail (Pefabloc; Sigma-Aldrich; final concentration 1 mg/ml). Four aliquots (each 250 μl) from each portion were removed immediately after the respective additions and transferred to low-adsorption Nunc tubes (VWR). The remaining plasma was kept cold (on ice) until analysis and served as ‘time 0’, while the aliquoted samples were kept at room temperature (27.1°C). Samples (100 μl) were then taken from each of the aliquots after 1 and 3 h, chilled immediately and kept cold until analysis on the same day. This procedure was repeated with a second set of tubes run in parallel, but using assay buffer (provided in the total GLP-1 sandwich ELISA [EZGLP1T-36K, see later description]) instead of plasma.
Biochemical analysis
Peptide
Synthetic GLP-1(9–36)NH2 was obtained from Bachem (Bubendorf, Switzerland). Prior to use, its structure and composition was verified by MS and quantitative amino acid analysis (duplicate determination) at the Department of Systems Biology, Enzyme and Protein Chemistry of the Danish Technical University (Kongens Lyngby, Denmark) and dissolved in phosphate buffer containing 1% (wt/vol.) human serum albumin (Calbiochem [San Diego, CA, USA], an affiliate of Merck) and stored at −20°C. Peptide concentrations in aliquots of the stock solution were verified using an in-house RIA employing a ‘side-viewing’ GLP-1 antiserum [26]. A fragment of GLP-1(9–36)NH2, FIAWLVKGR-NH2 [corresponding to GLP-1(28–36)NH2] was custom-synthesised by CASLO (Lyngby, Denmark).
Assays
Plasma levels of ‘total GLP-1’ [which includes both the (7–36)NH2 and (9–36)NH2 moieties and any N-terminally extended forms, including GLP-1(1–36)NH2 from the pancreas, if present] were quantified before and 15 min after oral glucose administration using two sandwich (two-site) ELISAs and one single-site C-terminal ELISA. One of the sandwich ELISAs employed a ‘side-viewing’ antibody as capture and a C-terminal HRP-conjugated antibody for detection (catalogue no. EZGLP1T-36K, Merck-Millipore, Billerica, MA, USA), while the antibody epitopes are not described for the other sandwich ELISA (total GLP-1 sandwich ELISA; Meso Scale Discovery, catalogue no. K150JVC-1, Rockville, MD, USA). For the single-site ELISA, also designed to measure ‘total GLP-1’, we used a newly developed customised xMAP-based assay (catalogue no. MMHMAG-84K, Merck-Millipore), which employed the same C-terminal antibody as used for detection in the Merck-Millipore sandwich ELISA, but without enzyme conjugation. Instead, the antibodies were coupled to fluorescent-coded magnetic beads (MagPlex-C Microspheres; Millipore). After the analyte was bound to the antibody-coupled bead, a biotinylated detection antibody was added, followed by incubation with streptavidin–phycoerythrin conjugate. Subsequently, the beads were subjected to flow cytometry-based detection using a Luminex laser-based analyser (Luminex 200; Luminex, Austin, TX, USA). The median fluorescent intensities from eight calibrators were used to interpolate concentrations in plasma samples using five-variable logistic regression.
Plasma levels of GLP-1(9–36)NH2 were assessed using a specific two-site sandwich ELISA (prototype, not yet commercially available; code name JP27788) from IBL (Hamburg, Germany). Total GLP-1 in the venous effluent from the perfused small intestine and in tissue biopsies from the gastrointestinal tract was measured using the EZGLP1T-36K (see above) and by a validated in-house C-terminally-directed RIA (code name 89,390 [27]). Plasma samples from oral gavages were also subjected to two-site ELISAs for measurement of insulin (Crystal Chem, Downers Grove, IL, USA), glucagon (Mercodia, Uppsala, Sweden) and glucose-dependent insulinotropic peptide (GIP; catalogue no. EZRMGIP-55K, Merck-Millipore). All provided quality controls were within the expected ranges, and all commercial analyses were performed according to manufacturers’ protocols.
MS-based proteomics
Pooled plasma (500 μl) from the in vivo degradation study [injection of 800 fmol GLP-1(9–36)NH2] was purified and analysed in technical triplicates using a validated platform for the detection of low-abundant peptides, as previously described [20]. We employed the ‘unspecific search’ option (assuming no enzymatic specificity for peptides between six and 29 amino acids) and searched the purified plasma fraction against the GLP-1 sequence as well as a list of common contaminants provided with MaxQuant (www.coxdocs.org/doku.php?id=maxquant:common:download_and_installation; version 1.5.4.3) [28]. To assess the presence of potential GLP-1 in vivo, cleavage products removed peptides that could have been derived from chymotrypsin (assuming N-terminal cleavage of L, M, F, W and Y). Identified peptides (at least two valid values in technical triplicates) were mapped to GCG, and the confidence of identification is provided via the Andromeda score [29].
Statistics
The experimenters were blind to outcome assessment but not to group assignment. To assess distribution and homoscedasticity in datasets, we applied the Shapiro–Wilk test (swilk command) and drafted residual plots. AUCs were calculated using the trapezoidal rule, and for net AUC we used ‘baseline subtracted data’ that included both increments and decrements. One-way ANOVA, corrected by a post hoc analysis (Sidak) for multiple testing, was used for testing differences between more than two groups of data. Unpaired two-sided t tests were used to assess differences between two groups. Data are expressed as mean ± SEM. A p value of <0.05 was considered significant. Calculations were made using GraphPad Prism (version 6.04 for Windows; GraphPad Software, La Jolla, CA, USA). The Adobe CS6 software suite (Adobe, San Jose, CA, USA) was used for illustrations.
Results
Secretory profiles of gastrointestinal and pancreatic hormones during oral administration of glucose or water in conscious mice
Oral glucose gavage resulted in robust (p < 0.001) increases in blood glucose that peaked 10 min after administration (baseline 8 ± 1 vs 24 ± 1 mmol/l) (Fig. 2a). Blood glucose levels were significantly (p < 0.001) lower during oral administration of water (peak level 9 ± 3 mmol/l) compared with glucose, but baseline values did not differ.
Oral glucose resulted in a twofold increase in plasma levels of total immunoreactive GLP-1 [(1−/7−/9–36)NH2] (p < 0.01) (Fig. 2b) compared with baseline, but only at 2 min, when analysed using the sandwich ELISAs. A similar pattern was observed in mice receiving water (Fig. 2b; the data depicted were obtained using the EZGLP1T-36K, but results were similar with K150JVC-1 sandwich ELISA [data not shown]). Using the customised C-terminally directed single-antibody assay (MMHMAG-84K), the secretory profile of GLP-1 (Fig. 2c), with a peak after 10 min (60 pg/ml, ~20 pmol/l; reported in pg/ml rather than pmol/l, as the exact molarity of the peptide picked up by this assay is unknown), was in sharp contrast to the results obtained using the sandwich ELISA (EZGLP1T-36K) for GLP-1 measurement (Fig. 2b). Biopsies from mouse stomachs contained low but detectable concentrations of GLP-1 (10 ± 2 pmol/g; well above the lower limit of detection of ~0.1 pmol/g) compared with the duodenum (31 ± 11 pmol/g) and distal ileum (74 ± 21 pmol/g).
Plasma GIP levels also peaked 10 min after glucose administration. There were no marked GIP changes after the administration of water (Fig. 2d). Plasma glucagon concentrations peaked at 2 min after stimulation in both groups, followed by a decrease (Fig. 2e). Glucose resulted in robust increases in plasma insulin levels, peaking at 10 min, whereas minimal changes were seen after water (Fig. 2f).
GLP-1 is secreted from the perfused small intestine in mice in response to an intraluminal glucose load
Luminal glucose (20%) stimulation resulted in long-lasting threefold increases in GLP-1 secretion (p < 0.001; Fig. 3a and ESM Fig. 2) independently (p = 0.76) of how GLP-1 was measured (C-terminal RIA: 89,390, vs sandwich ELISA: EZGLP1T-36K).
GLP-1(9–36)NH2 is rapidly degraded in vivo
Injection (i.v.) of GLP-1(9–36)NH2 in mice did not (p = 0.67) affect blood glucose compared with injection of isotonic saline (Fig. 3b, ESM Fig. 3a). Immunoreactive GLP-1 concentrations measured with the GLP-1 sandwich ELISA (EZGLP1T-36K) and the (9–36)NH2 specific ELISA increased within the first minute after injection of GLP-1(9–36)NH2, falling quickly thereafter to reach baseline 12 min after injection (ESM Fig. 3b). However, when the same samples were analysed using the C-terminally directed single-antibody ELISA, concentrations remained higher than at baseline (p < 0.001) for the duration of the experiment. Incremental AUCs mirrored these differences, being approximately threefold higher (p < 0.001) for the C-terminal assay compared with the sandwich ELISAs (ESM Fig. 3c). Immunoreactive GLP-1 levels were unchanged in mice receiving saline (ESM Fig. 3c). In mice with prior administration of candoxatril (a selective NEP 24.11 inhibitor, 5 mg/kg) immunoreactive GLP-1 concentrations were significantly higher (p < 0.001) compared with mice with prior administration of saline (Fig. 3c,d).
In vitro incubations with GLP-1(9–36)NH2
In control (buffer) experiments, GLP-1(9–36)NH2 was stable over 3 h (measured with the GLP-1 sandwich ELISA, EZGLP1T-36K) and concentrations were not significantly affected by the inclusion of protease inhibitors (Fig. 3e). In contrast, in mouse plasma (heparin), GLP-1(9–36)NH2 concentrations measured with the same assay were significantly (p < 0.01) lower after 1 h of incubation at room temperature and decreased even further after 3 h (Fig. 3f). Addition of a DPP-4 inhibitor (valine pyrrolidide) had no effect, whereas both an NEP 24.11 inhibitor (phosphoramidon) and an inhibitor cocktail (Pefabloc, a small molecule non-selective serine protease inhibitor) inhibited GLP-1(9–36)NH2 degradation and stabilised concentrations (Fig. 3f). Similar patterns were observed in pooled mouse plasma collected with EDTA (data not shown).
An MS-based platform identifies fragments consistent with NEP 24.11 cleavage of GLP-1
Multiple peptide fragments were identified in vivo, whereas none were identified in the parallel buffer experiment (Fig. 4). One fragment (FIAWLVKGR) corresponding to the C-terminus of GLP-1 [GLP-1(28–36)NH2] was synthesised and subsequently measured using the C-terminal ELISA (MMHMAG-84K) and the sandwich GLP-1 ELISA (EZGLP1T-36K) used in the previous experiments. This fragment showed cross-reactivity of 45 ± 12% in the C-terminal ELISA, but only 3 ± 2% in the sandwich ELISA (both in assay buffer).
Discussion
Here, we demonstrate that, in addition to degradation by DPP-4, GLP-1 in mice undergoes extremely fast endoproteolytic metabolism (probably mediated by NEP 24.11). Accordingly, the dynamics of GLP-1 secretion in vivo in mice can be estimated accurately only by C-terminal assays, whereas sandwich ELISAs provide only weak reflections of the actual secretion (Fig. 1).
Accurate estimation of GLP-1 secretion is a delicate matter and is further complicated by the fact that several commercially available assays are relatively unspecific and/or insensitive [30]. In addition, they often require high sample volumes (100–700 μl), rendering meaningful estimation of GLP-1 secretion at high time resolution impossible in mice (because of the low blood volume that can be obtained). Previous studies in mice [13,14,15,16,17,18,19] have estimated GLP-1 secretion in vivo by measuring ‘before vs post stimulation concentrations’ (typically at 0 and 15 min after the administration of a test substance). In one study, intact GLP-1 [(7–36)NH2] (measured using the sandwich ELISA from Linco Research, St Charles, MO, USA) concentrations of approximately 30 pmol/l peaked around 15 min after oral stimulation [31], strongly contrasting to the levels obtained by others [32,33,34,35] using sandwich ELISA techniques (which usually measure concentrations around 0 pmol/l), raising doubts as to the validity of this measurement. Others have used sandwich ELISAs (similar to those described here) and have also reported a rapid increase in immunoreactive GLP-1 within the first few minutes [36, 37]—similar to the glucagon profile described here. Such rapid increases may be due to cross-reactivity in the sandwich assays [30] with the (inactive) pancreatic isoform GLP-1(1–36)NH2, which is co-secreted with glucagon (probably in response to acute stress elicited by the gavage procedure). However, as demonstrated here, GLP-1 is also produced in the gastric mucosa of mice, although at much lower levels than in the small intestine, but nevertheless raising the possibility that the rapid (1–2 min) GLP-1 response could derive from the stomach rather than, or in addition to, pancreatic GLP-1(1–36)NH2 secretion. The development of a specific and sensitive low-volume assay for GLP-1(1–36)NH2 will be required to clarify this possibility, but the similar profiles of glucagon, measured using a validated assay for pancreatic (as opposed to gut) glucagon, support the hypothesis that the early immunoreactive GLP-1 peak may be due to GLP-1(1–36)NH2 from the pancreas.
Given that glucose is a GLP-1 secretagogue, the observation that the early immunoreactive GLP-1 peak actually preceded the peak in blood glucose levels made us question the suitability of the sandwich ELISAs for measuring GLP-1 in mice. Previously validated sandwich total GLP-1 ELISAs [30] have been shown to be reliable for measuring total GLP-1 in humans, presumably because GLP-1(9–36)NH2 is degraded relatively slowly in humans [6], and this also seems to be the case in rats [38]. We therefore hypothesised that, in mice, GLP-1(9–36)NH2 might undergo further rapid endoproteolytic cleavage, thereby precluding assessment of GLP-1 secretion in vivo by methods based on the measurement of full-length GLP-1(9–36)NH2 (e.g. sandwich ELISAs). Although it has been established that NEPs can degrade GLP-1(7–36)NH2 and (9–36)NH2 in vitro [11, 39, 40], we can now show that this occurs (in vivo) in mice with extreme rapidity and independent of DPP-4, consistent with the recent finding that NEP 24.11 knockout mice have higher plasma levels of GLP-1 [41] and that NEP 24.11 is ubiquitously expressed in endothelial cells [42]. Using a library of immunoassays and a sensitive MS-based platform [20], we have identified fragment(s) identical to the anticipated sequences that would be produced by endoproteolytic cleavage of GLP-1(9–36)NH2 by the NEP 24.11 enzyme [11], including ‘DVSSYLEGQAAKE’ [GLP-1(15–27)NH2] and ‘FIAWLVKGR-NH2’ [GLP-1(28–36)NH2], consistent with cleavage of GLP-1 in the mid region of the peptide (EGTFTSDVSSYLEGQAAKE-FIAWLVKGR); in support of this, inhibition of NEP 24.11 (by phosphoramidon and candoxatril) significantly attenuated degradation of GLP-1(9–36)NH2 in mouse plasma (when measured by a two-site sandwich ELISA). Notably, GLP-1(9–36)NH2 was stable when incubated in assay buffer, suggesting that the observed degradation in plasma was dependent on proteases present in plasma, rather than representing non-specific instability or analytical inadequacies. Theoretically, the C-terminal fragment, GLP-1(28–36) amide, should be measurable by C-terminal analysis but not with the sandwich ELISAs; this was demonstrated to be the case, using a synthetic replica of the fragment. Accordingly, the new customised C-terminal ELISA revealed preserved GLP-1 immunoreactivity in the in vitro experiments and secretory profiles of GLP-1 in vivo, which, unlike those obtained with the sandwich ELISAs, correlated to those of glucose absorption (blood glucose), GIP and insulin in a physiologically meaningful manner.
It has been suggested that GLP-1(9–36)NH2 may have effects on glucose homeostasis [43] and on the cardiovascular system [44,45,46]. In rodents, fragments of the GLP-1 metabolite may also have glucoregulatory effects, possibly mediated through hepatocytes [39], in line with previous observations of degradation of the GLP-1 metabolite [10, 40]. In humans, using the same specific sandwich ELISA as applied in this study, GLP-1(9–36)NH2 does not seem to be subject to the same rapid degradation, since the GLP-1 secretory profiles obtained with this assay (in response to oral glucose administration) are comparable with those obtained using a single-site C-terminal specific RIA [30]. Consequently, the current study indicates that the degradation rate of GLP-1 differs across species, and that accurate estimation of GLP-1 secretion in rodents (particularly in mice) requires assays that can cope with this. C-terminal assays may be sensitive to species-dependent differences in amidation ratios and, as such, may underestimate the secretion of GLP-1 if targeting glycine-extended GLP-1 forms, which could be true for rats but not mice [22]. The most versatile assay would not discriminate between amidated and glycine-extended forms.
In conclusion, GLP-1(9–36)NH2 undergoes further rapid degradation in mice, most likely by NEP 24.11. This contrasts to its relative stability in some other species, including humans. Therefore, estimation of GLP-1 secretion in mice cannot be made by measuring intact GLP-1(9–36)NH2 levels, but should instead be assessed using C-terminally directed methods capable of measuring the fragment FIAWLVKGR [GLP-1(28–36)NH2], which was identified in plasma in vivo.
Abbreviations
- DPP-4:
-
Dipeptidyl peptidase-4
- GIP:
-
Glucose dependent insulinotropic peptide
- GLP-1:
-
Glucagon-like peptide-1
- NEP:
-
Neutral endopeptidase
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Acknowledgements
We wish to thank G. Olesen and H. Berg Rasmussen (Department of Psychiatry, Sankt Hans Hospital, Roskilde, Denmark) for assistance with the Luminex instrument.
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The datasets generated during and/or analysed during the current study are available from the corresponding author on reasonable request.
Funding
Funding for this research was provided by the NNF Center for Basic Metabolic Research, University of Copenhagen (NNF application number: 13,563; Novo Nordisk Foundation, Denmark), EliteForsk Rejsestipendiat (2016), The Danish Council for Independent Research (DFF – 1333-00206A), the Danish Diabetes Academy (PhD funding), the Augustinus Foundation 14–0962, Aase og Ejnar Danielsens Fond, Mærsk Fonden, Holger Rabitz fond, Læge Johannes Nicolaj Krogsgaard og hustru Else Krogsgaards minde-legat for medicinsk forskning og medicinske studenter ved Københavns Universitet, the European Molecular Biology Organization and the European Foundation for the Study of Diabetes.
Duality of interest
The authors declare that there is no duality of interest associated with this manuscript. The authors’ (JJH and NJWA) collaboration with Mercodia, regarding measurement of glucagon in humans and in mice, has no relation to the current study. The kits from Mercodia and other companies used in the current study were not complimentary or given at reduced rates, but were obtained at the given market price.
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JAW, NJWA, JP and JJH contributed substantially to the concept and design of the study. All authors contributed substantially to the analysis and interpretation of the data. JAW, NJWA and REK drafted the manuscript. SLJ, DH, JP, EPJ, KDG, MW-S, AØ, CFD, MM, HK, BH and JJH critically revised the manuscript for important intellectual content. All authors have provided approval of the final version to be published. JJH is responsible for the integrity of the work as a whole.
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Windeløv, J.A., Wewer Albrechtsen, N.J., Kuhre, R.E. et al. Why is it so difficult to measure glucagon-like peptide-1 in a mouse?. Diabetologia 60, 2066–2075 (2017). https://doi.org/10.1007/s00125-017-4347-7
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DOI: https://doi.org/10.1007/s00125-017-4347-7