Abstract
Many fish species undergo natural starvation periods. Adaptation to starvation is possible through the activation of behavioral, biochemical and physiological mechanisms. Knowledge of the effect of dietary nutrients on the intermediary metabolism during starvation and refeeding can be useful to improve fish health and optimize aquaculture production. To analyze the effect of dietary nutrients on liver metabolism of Siberian sturgeon (Acipenser baerii) submitted to starvation and refeeding, four isoenergetic diets differing in nutrient composition were designed: LP-St (38 % protein, 12 % lipid, 36 % carbohydrate), HP-St (44 % protein, 10 % lipid, 30 % carbohydrate), LP-L (38 % protein, 18 % lipid, 25 % carbohydrate) and HP-L (44 % protein, 16 % lipid, 22 % carbohydrate). Four groups of fish were fed 3 weeks to satiety with the corresponding diet, starved for 2 weeks and then refeed 5 weeks to satiety on the same diet. Starvation mobilized the hepatic lipid store to a greater extent than glycogen. Starvation increased superoxide dismutase activity irrespective of the diet, while low protein diets (LP-St and LP-L) increased catalase activity. The oxidative damage decreased after 5 weeks of refeeding. Refeeding the starved fish on the HP-St diet promoted the greatest growth performance. In addition to reporting for the first time the effect of diet composition on growth, liver composition and antioxidant activities in Siberian sturgeon submitted to starvation and refeeding, our findings suggest that refeeding on HP-St diet stimulated the use of dietary carbohydrates and allowed a protein sparing effect in Siberian sturgeon.
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Introduction
Starvation periods are common in fish species (Morales et al. 2004). Starvation refers to the biological condition wherein an animal, otherwise willing or able to eat, is unable to do so as a result of some extrinsic limitation on food resources (McCue 2010). It can be induced artificially in commercial fish farms for decreasing water pollution, disease management and optimizing the feeding strategy to reduce the production cost (Caruso et al. 2012).
Under fed conditions, fish grow and increase the store of energy reserves. On the contrary, fasting leads to the mobilization of fuel from the body store and mass loss (Power et al. 2000; Morales et al. 2004). The reduction rate of muscle mass is extremely variable due to different energy requirements depending on body weight and phylogenetic affiliation (Garland et al. 2005). Some organs, such as the liver, can tolerate large reductions in mass during the starvation period by controlling fuel storage and nutrient mobilization (Metón et al. 2003; Pérez-Jiménez et al. 2007).
During fasting, most species use liver glycogen as the first substrate to obtain energy (Viegas et al. 2012). In parallel with liver glycogen exhaustion, lipid reserves are also used as a fuel. When both glycogen and lipid supplies are nearly depleted, protein is mobilized (Navarro and Gutierrez 1995; Metón et al. 2003). However, some fish species, such as Salmo gairdneri and Notopterus notopterus, use lipids and protein as energy substrates during starvation, without affecting significantly the hepatic glycogen store (Narasimhan and Sundararaj 1971; Leatherland and Nuti 1981; Pérez-Jiménez et al. 2007). In fish, the use of body glycogen, lipid and protein to obtain energy during starvation varies according to the species, period of food deprivation and the diet composition prior to fasting (Hilton 1982).
It was reported that caloric restriction can induce oxidative stress in fish (Chatzifotis et al. 2011). Oxidative stress occurs when reactive oxygen species (ROS) generation exceeds its removal and may lead to cell death (Sies 1986). By catalyzing the conversion of superoxide anion into molecular oxygen and water, superoxide dismutase (SOD; EC 1.15.1.1) and catalase (CAT; EC 1.11.1.16) are key antioxidant enzymes that were previously shown to be present in the fish liver (Aras et al. 2009). Some studies addressed the effect of food deprivation on oxidative stress and antioxidant defenses (Feng et al. 2011; Bayir et al. 2011). However, the impact of diet composition on antioxidant activities in fish submitted to starvation–refeeding remains largely unknown.
Although diet composition and feeding regimes may have a major impact on fish health and production, little is known regarding to optimization of feeding strategies in cultured fish species with a marked commercial interest, such as sturgeon, exposed to starvation and refeeding. To increase the current knowledge about the effect of diet composition and feeding regime on somatic and metabolic parameters of Siberian sturgeon (Acipenser baerii), in the present work we evaluated growth performance, liver composition and activity of liver antioxidant enzymes in Siberian sturgeon submitted to starvation and refeeding on various diets differing in nutrient composition.
Materials and methods
Rearing procedures
A group of 180 Siberian sturgeon juveniles (initial body weight 30 ± 5 g) were obtained from International Sturgeon Research Institute (Gilan, Iran) and randomly supplied in 12, 500-L circular fiberglass tanks (n = 15 per tank) in a flow-through system containing treated river water with continuous aeration. Fish were fed on commercial pellets (BIOMAR, France, 1.9 mm) for 1 week while they acclimated to the experimental conditions (Bagherzadeh Lakani et al. 2013). Tanks were located outdoors and subjected to natural photoperiod of approximately 12:12 h (light: dark) cycle. Every day, all tanks were cleaned and siphoned to remove debris. Temperature, dissolved O2, pH value and flow rate were maintained at 22 ± 4 °C, 7.1 ± 1.5 mg L−1, 7–8 and 4.5 ± 0.5 L min−1, respectively. Four groups of fish were fed manually to satiety with the corresponding experimental diet three times a day (8:30, 15:00 and 21:30 h) for 3 weeks, starved for 2 weeks and then refed for 5 weeks on the same diet and conditions. Three tanks were used for each condition.
Feeding trial
Ingredients and chemical composition of experimental diets used in the present study are given in Table 1. Four isoenergetic diets (gross energy 19.9 ± 0.4 kJ g−1 dm) were formulated with different levels of protein, lipids and carbohydrates. Fishmeal was used as protein source. Diets were named LP-St (low protein, 38 %—high carbohydrate, 36 %), HP-St (high protein, 44 %—high carbohydrate, 30 %), LP-L (low protein, 38 %—high lipid, 18 %) and HP-L (high protein, 44 %—high lipid, 16 %). Dry ingredients were weighed, ground and mixed thoroughly. Fish oil, sunflower oil, lecithin and water were added to the dry ingredients and mixed again, until dough was formed. Dough was pelleted in 2 mm and dried in a hot air oven (Hootakhsh, Tehran, Iran) at 60 °C for 5–6 h. The diets were broken up and sieved into proper pellet size, packed and stored at −20 °C until used.
Sample preparation
Sampling was performed at week 3 (end of feeding period), 5 (after 2 weeks of starvation) and 10 (after 5 weeks of refeeding). Two animals of each tank (six per dietary treatment) were anaesthetized with clove powder (500 mg L−1) (Yarmohammadi et al. 2012) and then killed by a sharp blow in the head (Pérez-Jiménez et al. 2009). Liver tissue was dissected using clean equipment on ice (0 °C), weighted, washed, immediately frozen in liquid nitrogen and kept at −80 °C until further analysis. Fish hepatosomatic index (HSI) was measured by the following equation (Higgs et al. 2009):
Treatment of the samples
Liver tissues were homogenized (1:10, w/v) in homogenization buffer containing 100 mM potassium phosphate buffer (pH 7.4), 100 mM KCl and 1 mM EDTA at 0–4 °C using an electric homogenizer (WIGGEN, D500, Germany) for 1.5 min. Homogenates were centrifuged at 10,000 g using a Hermle Z36HK centrifuge (Hermle Labortechnik, Germany) for 35 min at 4 °C. Supernatants were used to determine glycogen and measure enzyme activity (Atli and Canli 2010). All chemicals used in this study were obtained from Sigma-Aldrich (USA) and Merck (Germany).
Chemical analysis
Chemical composition (crude protein, lipid and moisture) of the experimental diets and fish livers was determined using the following (AOAC 2005) procedures: total protein content (N × 6.25) using an automatic Kjeldahl system (230-Hjeltec Analyzer; Foss Tecator, Hoganas, Sweden) and total lipid with an automatic Soxtec system (2050-FOSS; Sweden). Moisture was determined by drying at 105 °C for 24 h in an oven (D-63450; Heraeus, Hanau, Germany), and ash by burning in a muffle furnace (Isuzu, Tokyo, Japan) at 550 °C for 6 h. Glycogen was assayed using the BDU-GLY96 ELISA kit (Zellbio, Germany). In brief, the assay is based on glycogen hydrolyzation into glucose. Glucose oxidation forms an intermediate that reduces a colorless robe to a colored product with strong absorbance at 620 nm. The glycogen content is expressed as milligrams of glucose equivalents per gram of fresh liver tissue.
Determination of enzyme activities
SOD and CAT activities were determined using spectrophotometric methods. SOD was assayed with the ZB-SOD96 kit (ZellBio GmbH, Germany). SOD activity unit was considered as the amount of the sample that catalyzed decomposition of 1 μmol of O2− into H2O2 and O2 per minute. Absorbance was recorded at 550 nm.
CAT was assayed using the ZB-CAT96 kit (ZellBio GmbH, Germany). CAT activity unit was considered as the amount of the sample that catalyzed decomposition of 1 μmol of H2O2 into H2O and O2 per minute. Absorbance was recorded at 405 nm.
Total soluble protein was measured by the Bradford method (1976) using bovine serum albumin as a standard. Enzyme activities were expressed as specific activity (U mg−1 protein). All the enzymatic assays were run in triplicate.
Statistical analysis
Data were checked for normality (Kolmogorov–Smirnov test) and homogeneity of variances prior to their comparison. Data were analyzed by one-way and two-way (diet and condition as the main factors) ANOVA using a computer program (IBM SPSS Statistics version 22, Armonk, NY, USA). Statistical differences among mean values with one independent variable were analyzed by one-way ANOVA performing mean comparisons with Duncan’s test at a reliability level of 0.05. To determine homogeneous subsets of values with two independent variables, two-way ANOVA was performed using the Scheffé post hoc test (P < 0.05).
Results
Growth performance and HSI
The growth performance of Siberian sturgeon juveniles was affected by diet composition in fish submitted to starvation and refeeding (Table 2). Feeding on HP-St and LP-St resulted in the highest (182 ± 7.9 g) and lowest (158 ± 10 g) final body weight, respectively. Accordingly, feeding on HP-St promoted significantly higher weight gain values than in the group of fish fed diet LP-St during 5 weeks of refeeding. The highest and lowest FCR values were presented by fish fed diets LP-St and HP-St, respectively. Albeit not significant, it was observed a tendency to present higher specific growth rate (SGR) values in the fish supplied with high protein diets during refeeding.
Two weeks of starvation significantly decreased HSI irrespective of the diet. After 3 weeks of feeding and 5 weeks of refeeding, fish fed with high carbohydrate diets (HP-St and LP-St) presented the highest HSI values. In all treatments, the lowest HSI value was found in the group of fish fed diet HP-L (Fig. 1).
Liver composition
Liver composition of Siberian sturgeon was significantly affected by diet composition and nutritional status (Fig. 2). After 3 weeks of feeding, a trend to present higher hepatic glycogen levels was found in the fish fed high carbohydrate diets (LP-St and HP-St). Starvation for 2 weeks significantly decreased liver glycogen reserves, reaching similar values irrespective of the diet, about 13–14 mg g−1 liver. Five weeks of refeeding were not enough to recover hepatic glycogen levels similar to those observed previous to starvation, and no significant differences in liver glycogen content were found among the groups of fish fed different diets.
Two weeks of starvation significantly fell down hepatic lipid reserves except in the group LP-L. Five weeks of refeeding led to recover liver lipid reserves in all treatments to levels higher than in 3 week fed fish. After both 3 weeks of feeding and 5 weeks of refeeding, the supply of low protein diets (LP-St and LP-L) significantly increased liver fat compared to fish fed high protein diets (HP-St and HP-L).
Concerning the hepatic protein content, no significant effect was observed between 3 week fed fish and 2 week starved animals. However, refeeding significantly increased liver protein irrespective of the diet. In all conditions, the fish fed diet LP-L exhibited the higher hepatic protein content.
CAT and SOD specific activities in liver
The nutritional status and diet composition significantly affected liver CAT and SOD activities (Fig. 3a, b). A trend to increase the specific activity of CAT in juveniles fed with LP-L and LP-St diets was observed after 2 weeks of starvation, while almost no change was observed in the fish fed high protein diets (HP-St and HP-L) (Fig. 3a). Compared to starved fish, 5 weeks of refeeding with low protein diets (LP-St and LP-L) significantly decreased CAT activity. The lower CAT activity levels after refeeding were found in the fish fed diet HP-L.
Starvation significantly increased SOD activity in the liver of fish fed the four experimental diets. After 5 weeks of refeeding, a trend to recover the values found in 3 week fed fish was observed in all treatments with the exception of fish fed diet HP-St (Fig. 3b).
Discussion
In recent years, some wild populations of Caspian Sea sturgeons are among critical endangered fish species (IUCN Red Data List, 2015), because of overfishing for meat and caviar production, destruction of their spawning grounds and water pollution (Babaei et al. 2011). Therefore, research efforts have focused on Siberian sturgeon for developing aquaculture programs and reducing overfishing of native sturgeons. The aim of this study was to determine the appropriate feeding schedule when using starvation periods in order to improve production, maximize growth and produce less oxidative damage to Siberian sturgeon in culture.
Previous studies reported influence of diet composition on growth performance in Siberian sturgeon (Rónyai et al. 2002; Guo et al. 2012) and other sturgeons (Abedian Kenari et al. 2009; Hosseini et al. 2010). However, it remains largely unknown the effect of the nutrient composition of the diet on physiological responses during starvation and refeeding in this species. In the present study, the higher WG after refeeding was found in the group of fish fed on the high protein/high carbohydrate diet (HP-St). This finding suggests that dietary carbohydrate may promote a faster recovery of BW than dietary lipids after a food deprivation period in Siberian sturgeon. Concerning the protein content of the diet, our findings are consistent with the optimal dietary protein level reported for maximal growth for Acipenser sinensis (about 40–45 %; Xiao et al. 1999) and A. persicus (40 %; Mohseni et al. 2007). In hybrid sturgeon (Acipenser baerii ♀ × A. gueldenstaedtii ♂) optimal dietary protein was estimated at 37 % (Guo et al. 2012). However, refed fish show a fast weight recovery, mainly supported by the rapid restoration of their metabolic profile (Furne et al. 2012).
In Siberian sturgeon, the higher HSI and hepatic glycogen values were found in fish fed high carbohydrate diets (HP-St and LP-St). Positive correlation between HSI and liver glycogen content with dietary carbohydrate levels has been well documented in Acipenser baerii (fed on gelatinized starch) (Médale et al. 1991), white sturgeon (Acipenser transmontanus) (fed on high d-glucose diet) (Fynn-Aikins et al. 1992) and other fish species, such as Sparus aurata (Metón et al. 1999). Similarly as in the present study, a significant reduction in HSI of Siberian sturgeon during starvation was observed previously when feeding on commercial pellets before fasting (Ashouri et al. 2013). Decreased HSI was also observed in starved white sturgeon (Hung et al. 1997b), brown trout, Salmo trutta (Bayir et al. 2011) and gilthead sea bream (Metón et al. 1999). Refeeding increased HSI in all groups of fish. However, the higher HSI values were observed in Siberian sturgeon fed high carbohydrate diets, while feeding a high protein/high lipid diet (HP-L) resulted in the lowest HSI levels. During refeeding, hyperphagia can prompted some metabolic pathways to recover the metabolic profile and reestablish the tissue reserves (Furne et al. 2012), probably resulting in increased HSI and body weight.
In many fish species, glycaemia maintenance during food deprivation is directly related to the ability to mobilize liver glycogen, at least during the initial stages of starvation (Pérez-Jiménez et al. 2007). Hepatic glycogen, when required, is enzymatically broken down to glucose and transported to peripheral tissues. Our findings indicate that after starvation, hepatic glycogen modestly decreased in all treatments (notably in the fish fed low carbohydrate diets). In contrast, liver glycogen is mobilized as early as after 5–20 days of fasting in A. naccarii (Furne et al. 2012) and white sturgeon (Hung et al. 1997b).
More than 60 % of liver dry mass (230–330 mg g−1 liver) of Siberian sturgeon liver are lipids. Similar liver fat content is found in white sturgeon (300–370 mg g−1 liver) (Fynn-Aikins et al. 1992). After 3-week feeding, the lowest lipid content was present in the liver of Siberian sturgeon fed the high protein/high carbohydrate diet (HP-St). Consistently, there is convincing evidence that high protein diets increase fat loss compared to diets with lower protein content (Halton and Hu 2004), as it is the case in hybrid sturgeon (Guo et al. 2012). Lipids have a major role in fish that do not mobilize significant levels of liver glycogen during starvation (Sheridan and Mommsen 1991). Most animals are able to tolerate a 20–70 % loss of total body lipid content during starvation (McCue 2010). The use of the lipid store during food deprivation depends on the species, the lipid-reserve tissue and mobilization of other energy supplies such as glycogen (Furne et al. 2012). Starvation significantly decreased liver fat in Siberian sturgeon. Besides, our findings argue for the mobilization of lipid store and to a lesser extend glycogen in the liver of 2 week starved Siberian sturgeon. These results suggest that the Siberian sturgeon liver may preferentially utilize lipids as an energy resource. Similar results were reported for channel catfish (Kim and Lovell 1995) and Adriatic sturgeon A. naccarii, where liver lipid also decreased more importantly than hepatic glycogen and protein (Furne et al. 2012). Furthermore, a greater utilization of sturgeon hepatic lipids for energy purposes during fasting may result from the high hepatic lipid content in this species (Furne et al. 2012). The time course of recovery in the liver differed for glycogen and fat after refeeding: liver lipid was significantly higher after 5 weeks of refeeding compared to the values observed before food deprivation, while the refeeding period was not enough to recover liver glycogen.
The hepatic protein content was less affected than liver fat by the nutritional condition and diet composition in Siberian sturgeon. Similarly, white sturgeon (Hung et al. 1997a) and Persian sturgeon (Mohseni et al. 2007) fed with diets differing in nutrient composition were reported to keep body protein relatively constant. Indeed, reduction in carcass protein content of white sturgeon after 10 weeks of fasting was much lower (9 %) than that of the lipid content (84 %) (Hung et al. 1997b), suggesting that sturgeon preferentially conserve muscle protein over lipids during food deprivation (Falahatkar et al. 2013).
Over the past few decades, the stress response of fish has been extensively investigated. However, the relationship between diet composition, fish stress and immune response as well as between feeding regime and immune response have received little attention (Caruso et al. 2011; Li et al. 2012). High lipid storage in sturgeon is rich in unsaturated fatty acids (García-Gallego et al. 1999), which exhibit a very strong tendency toward oxidation (Fang et al. 2003). The specific activities of antioxidant enzymes in Siberian sturgeon were low compared with other species. The lower oxygen consumption by sturgeon and its phylogenetic position (ancestral species exhibit less antioxidant activity) (Tappel et al. 1982) may explain these findings.
As with Siberian sturgeon, increased SOD activity has been described during starvation in Pseudo sciaenacrocea (Zhang et al. 2008) and brown trout (Bayir et al. 2011). These results suggest that the rate of O2·− generation increases during starvation.
CAT activity is associated with elevated concentrations of H2O2, which in turn is produced by SOD reaction. In the present study, starvation increased SOD activity irrespective of the diet, while low protein diets (LP-St and LP-L) resulted in high CAT activity values. Compared with starvation, our results indicate that the oxidative damage decreased after 5 weeks of refeeding. In contrast, Furne et al. (2009) reported that oxidative stress remained after 60 days of refeeding in liver and red blood cells of rainbow trout and sturgeon. The low antioxidant activities in the fish fed diet HP-L after refeeding may be related to the low HSI and low hepatic lipid content (as a free radical production inducer) observed in this group of fish.
In conclusion, our findings show for the first time that Siberian sturgeon juveniles experience metabolic adjustments to both starvation and refeeding, and that diet composition has a major impact on the metabolic responses to nutritional status. Growth performance and liver composition suggest that refeeding with a high protein/high carbohydrate diet stimulates the use of dietary carbohydrates, while allows sparing protein in Siberian sturgeon. Given that supply of diets with a significant amount of carbohydrates to sturgeon can diminish feeding costs and allow sparing protein without decreasing the growth performance after food deprivation periods, the results of the present study may be useful to improve feed management to achieve better nutrition efficiency and fish health.
References
Abedian Kenari A, Regenstein JM, Hosseini SV, Rezaei M, Tahergorabi R, Nazari RM, Kaboli SA (2009) Amino acid and fatty acid composition of cultured Beluga (Huso huso) of different ages. J Aquat Food Prod Technol 18:245–265
AOAC (2005) Official methods of analysis of the AOAC International, 18th edn. AOAC International, Gaithersburg
Aras NM, Bayir A, Sirkecioğlu AN, Bayir M, Aksakal E, Haliloğlu HI (2009) Seasonal changes in antioxidant defense system of liver and gills of Salmo trutta caspius, Salmo trutta labrax and Salmo trutta macrostigma. J Fish Biol 74:842–856
Ashouri G, Yavari V, Bahmani M, Yazdani MA, Kazemi R, Morshedi V, Fatollahi M (2013) The effect of short-term starvation on some physiological and morphological parameters in juvenile Siberian sturgeon Acipenser baerii (ActinopterygII: Acipenseriformes: Acipenseridae). Acta Ichtyol Piscat 43(2):145–150
Atli G, Canli M (2010) Response of antioxidant system of freshwater fish Oreochromis niloticus to acute and chronic metal (Cd, Cu, Cr, Zn, Fe) exposures. Ecotoxicol Environ Saf 73:1884–1889
Azarm HM, Kenari AA, Hedayati M (2013) Effect of dietary phospholipid sources and levels on growth performance, enzymes activity, cholecystokinin and lipoprotein fractions of rainbow trout (Oncorhynchus mykiss) fry. Aquac Res 44:634–644
Babaei SS, Abedian-Kenari A, Nazari R, Gisbert E (2011) Developmental changes of digestive enzymes in Persian sturgeon (Acipenser persicus) during larval ontogeny. Aquaculture 318:138–144
Bagherzadeh Lakani F, Sattari M, Sharifpour I, Kazemi R (2013) Effect of hypoxia, normoxia and hyperoxia conditions on gill histopathology in two weight groups of beluga (Huso huso). Casp J Environ Sci 11:78–84
Bayir A, Sirkecioglu N, Bayir M, Haliloglu HI, Kocaman EM, Aras NM (2011) Metabolic responses to prolonged starvation, food restriction, and refeeding in the brown trout, Salmo trutta: oxidative stress and antioxidant defenses. Comp Biochem Physiol Part B 159:191–196
Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72:248–254
Caruso G, Denaro MG, Caruso R, Genovese L, Mancari F, Maricchiolo G (2011) Response to short term starvation of growth, haematological, biochemical and non-specific immune parameters in European sea bass (Dicentrarchus labrax) and blackspot sea bream (Pagellus bogaraveo). Mar Environ Res 72:46–52
Caruso G, Denaro MG, Caruso R, Genovese L, Mancari F, Maricchiolo G (2012) Short fasting and refeeding in red porgy (Pagrus pagrus, Linnaeus 1758): response of some haematological, biochemical and non-specific immune parameters. Mar Environ Res 81:18–25
Chatzifotis S, Papadaki M, Despoti S, Roufidou C, Antonopoulou E (2011) Effect of starvation and re-feeding on reproductive indices, body weight, plasma metabolites and oxidative enzymes of sea bass (Dicentrarchus labrax). Aquaculture 316:53–59
Falahatkar B, Akhavan SR, Efatpanah I, Meknatkhah B (2013) Effect of winter feeding and starvation on the growth performance of young-of-year (YOY) great sturgeon, Huso huso. J Appl Ichthyol 29:26–30
Fang X, Watanabe Y, Adachi S, Matsumura Y, Mori T, Maeda H, Nakamura A, Matsuno R (2003) Microencapsulation of linoleic acid with low- and high-molecular-weight components of soluble soybean polysaccharide and its oxidation process. Biosci Biotechnol Biochem 67:1864–1869
Feng G, Shi X, Huang X, Zhuang P (2011) Oxidative stress and antioxidant defenses after long-term fasting in blood of Chinese sturgeon (Acipenser sinensis). Proc Environ Sci 8:469–475
Furne M, GarcÍa-Gallego M, Hidalgo MC, Morales AE, Domezain A, Domezain J, Sanz A (2009) Oxidative stress parameters during starvation and refeeding periods in Adriatic sturgeon (Acipenser naccarii) and rainbow trout (Oncorhynchus mykiss). Aquac Nutr 15:587–595
Furne M, Morales AE, Trenzado CE, Garcıa-Gallego M, Hidalgo MC, Domezain A, Rus AS (2012) The metabolic effects of prolonged starvation and refeeding in sturgeon and rainbow trout. Comp Biochem Physiol 182:63–76
Fynn-Aikins K, Hung SSO, Liu W, Li H (1992) Growth, lipogenesis and liver composition of juvenile white sturgeon fed different levels of D-glucose. Aquaculture 105:61–72
García-Gallego M, Sanz A, Domezain A, Higuera M (1999) Age-size influences on tissue-lipid quality of the sturgeon Acipenser naccarii from intensive culture. J Appl Ichthyol 15:261–264
Garland T, Bennett AF, Rezende EL (2005) Phylogenetic approaches in comparative physiology. J Exp Biol 208:3015–3035
Guo Z, Zhu X, Liu J, Han D, Yang Y, Lan Z, Xie S (2012) Effects of dietary protein level on growth performance, nitrogen and energy budget of juvenile hybrid sturgeon, Acipenser baerii♀ × A. gueldenstaedtii♂. Aquaculture 338–341:89–95
Halton TL, Hu FB (2004) The effects of high protein diets on thermogenesis, satiety and weight loss: a critical review. JACN 23:373–385
Hamza N, Mhetli M, Khemis IB, Cahu C, Kestemont P (2008) Effect of dietary phospholipids levels on performance, enzyme activities and fatty acid composition of pikeperch (Sander lucioperca) larvae. Aquaculture 275:274–282
Higgs DA, Sutton JN, Kim H, Oakes JD, Smith J, Biagi C, Devlin RH (2009) Influence of dietary concentrations of protein, lipid and carbohydrate on growth, protein and energy utilization, body composition, and plasma titres of growth hormone and insulin-like growth factor-1 in non-transgenic and growth hormone transgenic coho salmon. Aquaculture 286:127–137
Hilton JW (1982) The effect of pre-fasting diet and water temperature on liver glycogen and liver weight in rainbow trout, Salmo gairdneri Richardson, during fasting. J Fish Biol 20:69–78
Hosseini SV, Abedian-Kenari A, Regenstein JM, Rezaei M, Nazari RM, Moghaddasi M, Grant AAM (2010) Effects of alternative dietary lipid sources on growth performance and fatty acid composition of beluga sturgeon, Huso huso, juveniles. J World Aquac Soc 41:471–489
Hung SSO, Storebakken T, Cui Y, Tian L, Einen O (1997a) High-energy diets for white sturgeon (Acipenser transmontanus Richardson). Aquac Nutr 3:281–286
Hung SSO, Liu W, Li H, Storebakken T, Cui Y (1997b) Effect of starvation on some morphological and biochemical parameters in white sturgeon, Acipenser transmontanus. Aquaculture 151:357–363
Kim MK, Lovell RT (1995) Effect of restricted feeding regimens on compensatory weight gain and body tissue changes in channel catfish Ictalurus punctatus in ponds. Aquaculture 135:285–293
Leatherland JF, Nuti RN (1981) Effects of bovine growth hormone on plasma FFA concentrations and liver, muscle and carcass lipid content in rainbow trout, Salmo gairdneri Richardson. J Fish Biol 19:487–498
Li XF, Liu WB, Lu KL, Xu WN, Wang Y (2012) Dietary carbohydrate/lipid ratios affect stress, oxidative status and non-specific immune responses of fingerling blunt snout bream, Megalobrama amblycephala. Fish Shellfish Immunol 33:316–323
McCue MD (2010) Starvation physiology: reviewing the different strategies animals use to survive a common challenge. Comp Biochem Physiol Part A 156:1–18
Médale F, Blanc D, Kaushik SJ (1991) Studies on the nutrition of Siberian sturgeon, Acipenser baerii. II. Utilization of dietary non-protein energy by sturgeon. Aquaculture 93:143–154
Metón I, Mediavilla D, Caseras A, Cantó E, Fernández F, Baanante IV (1999) Effect of diet composition and ration size on key enzyme activities of glycolysis–gluconeogenesis, the pentose phosphate pathway and amino acid metabolism in liver of gilthead sea bream (Sparus aurata). Br J Nutr 82:223–232
Metón I, Fernández F, Baanante IV (2003) Short- and long-term effects of refeeding on key enzyme activities in glycolysis-gluconeogenesis in the liver of gilthead sea bream (Sparus aurata). Aquaculture 225:99–107
Mohanta KN, Mohanty SN, Jena JK, Sahu NP (2008) Optimal dietary lipid level of silver barb, Puntius gonionotus fingerlings in relation to growth, nutrient retention and digestibility, muscle nucleic acid content and digestive enzyme activity. Aquac Nutr 14:350–359
Mohseni M, Sajjadi M, Pourkazemi M (2007) Growth performance and body composition of sub-yearling Persian sturgeon, (Acipenser persicus, Borodin, 1897), fed different dietary protein and lipid levels. J Appl Ichthyol 23:204–208
Morales AE, Pérez-Jiménez A, Carmen Hidalgo M, Abellán E, Cardenete G (2004) Oxidative stress and antioxidant defenses after prolonged starvation in Dentex dentex liver. Comp Biochem Physiol Part C 139:153–161
Narasimhan PV, Sundararaj BI (1971) Effects of stress on carbohydrate metabolism in the teleost Notopterus notopterus (Pallas). J Fish Biol 3:441–451
Navarro I, Gutierrez J (1995) Fasting and starvation. In: Hochachka PW, Mommsen TP (eds) Biochemistry molecular biology fishes, vol 4. Elsevier Science, Amsterdam, pp 393–434
NRC (National Research Council) (1993) Nutrient requirements of warm water fishes and shellfishes (Revised edn). National Academy Press, Washington, p 225
Pérez-Jiménez A, Guedes MJ, Morales AE, Oliva-Teles A (2007) Metabolic responses to short starvation and refeeding in Dicentrarchus labrax. Effect of dietary composition. Aquaculture 265:325–335
Pérez-Jiménez A, Hidalgo MC, Morales AE, Arizcun M, Abellán E, Cardenete G (2009) Growth performance, feed utilization and body composition of Dentex dentex fed on different macronutrient combinations. Aquac Res 41:111–119
Power DM, Melo J, Santos CR (2000) The effect of food deprivation and re-feeding on the liver, thyroid hormones and transthyretin in sea bream. J Fish Biol 56:374–384
Rónyai A, Csengeri I, Váradi L (2002) Partial substitution of animal protein with full-fat soybean meal and amino acid supplementation in the diet of Siberian sturgeon (Acipenser baerii). J Appl Ichthyol 18:682–684
Sheridan MA, Mommsen TP (1991) Effects of nutritional state on in vivo lipid and carbohydrate metabolism of coho salmon, Oncorhynchus kisutch. Gen Comp Endocrinol 81:473–483
Sies H (1986) Biochemistry of oxidative stress. Angew Chem Int Ed Engl 25:1058–1071
Tappel ME, Chaudiere J, Tappel AL (1982) Glutathione peroxidase activities of animal tissues. Comp Biochem Physiol Part B 73:945–949
Viegas I, Carvahlo RA, Pardal MA, Jones JG (2012) Advances and application of tracer measurements of carbohydrates metabolism in fish. In: Türker H (ed) New advances and contributions to fish biology. Intech, pp 247–270. http://www.intechopen.com/books/new-advances-and-contributions-to-fish-biology/advances-and-applications-of-tracer-measurements-of-carbohydrate-metabolism-in-fish. Accessed 28 June 2015
Xiao H, Wang JS, Wen ZH, Lu XB, Liu H (1999) Studies on suitable nutrient content in formulated diet for juvenile Acipenser sinensis. J Fish Sci China 6:33–38 (with English abstract)
Yarmohammadi M, Shabani A, Pourkazemi M, Soltanloo H, Imanpour MR (2012) Effects of starvation and re-feeding on growth performance and content of plasma lipids, glucose and insulin in cultured juvenile Persian sturgeon (Acipenser persicus, Borodin 1897). J Appl Ichthyol 28:692–696
Zhang XD, Zhu YF, Cai LS, Wu TX (2008) Effects of fasting on the meat quality and antioxidant defenses of market-size farmed large yellow croaker (Pseudo sciaenacrocea). Aquaculture 280:136–139
Acknowledgments
The research was financially supported by Tarbiat Modares University (TMU, Iran). The authors would like to thank the International Sturgeon Research Institute of Caspian Sea (Gilan, Iran) for fish husbandry, the Cellular and Molecular Research Center of Shahid Beheshti University of Medical Sciences (Tehran, Iran) for technical support and Mazandaran Animal and Aquatic feed (Manaqua) Co. (Sari, Iran). We would like to thank Morteza Kamali for his kind technical help.
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Babaei, S., Abedian Kenari, A., Hedayati, M. et al. Effect of diet composition on growth performance, hepatic metabolism and antioxidant activities in Siberian sturgeon (Acipenser baerii, Brandt, 1869) submitted to starvation and refeeding. Fish Physiol Biochem 42, 1509–1520 (2016). https://doi.org/10.1007/s10695-016-0236-0
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DOI: https://doi.org/10.1007/s10695-016-0236-0