TY - JOUR
T1 - Conjugated linoleic acid differentially modulates growth, tissue lipid deposition, and gene expression involved in the lipid metabolism of grass carp
AU - Dong, Gui Fang
AU - Zou, Qi
AU - Wang, Huan
AU - Huang, Feng
AU - Liu, Xiao Chun
AU - Chen, Lu
AU - Yang, Chao Yu
AU - Yang, Yan ou
N1 - Funding Information:
The current study was supported by the National Natural Science Foundation of China (grant no. 31302195 ), the Natural Science Foundation of Hubei Province of China (grant no. 2011CDB225 ), and Hubei Collaborative Innovation Center for Animal Nutrition and Feed Safety, and International Science & Technology Cooperation Program of China (grant no. 2011DFG33280 ), and Major Science and Technology Program for Water Pollution Control and Treatment of Lake Chaohu (grant no. 2012ZX07103003-02-02 ). All authors also thank the anonymous reviewers for their helpful suggestions.
PY - 2014/8/20
Y1 - 2014/8/20
N2 - Conjugated linoleic acid (CLA) has been shown to decrease body fat and increase lean tissue in mammals. However, limited data is available about the effect of CLA on the lipid content in fish tissue, and the mechanisms underlying the beneficial effects of CLA in fish are unknown. We hypothesized that dietary CLA may induce lipid-lowering effects in grass carp (Ctenopharyngodon idella) tissue, and the fat reduction effect was modulated by the expression of genes involved in the lipid metabolism. A 65-day growth trial was conducted to investigate the effect of CLA on the growth, tissue lipid deposition, and gene expression involved in the lipid metabolism of grass carp. Seven isonitrogenous and isolipidic diets were formulated: 0% CLA (control); 0.5% CLA (CLA0.5); 1% CLA (CLA1); 1.5% CLA (CLA1.5); 2% CLA (CLA2); 2.5% CLA (CLA2.5); and 3% CLA (CLA3).Results showed that only fish fed the CLA3 diet exhibited a significant reduction in feeding rate and specific growth rate than those of fish fed the control diet (P<. 0.05). Significant decreases in the lipid content in the liver, intraperitoneal fat, and muscle were observed in fish fed with 2.5% to 3% CLA, 1.5% to 3% CLA, and 2% to 3% CLA diets, respectively (P<. 0.05), compared to those fed with the control diet. Dose- and tissue-dependent changes were found in the mRNA expressions of fatty acid synthetase (FAS), acetyl-CoA carboxylase (ACC), lipoprotein lipase (LPL), hormone-sensitive lipase (HSL), peroxisome proliferator-activated receptor α (PPARα), peroxisome proliferator-activated receptor γ (PPARγ), and sterol regulatory element binding protein-1c (SREBP-1c). The mRNA expressions in most of the genes examined in the liver, foregut, intraperitoneal fat and muscle were highly sensitive to dietary CLA. Our results suggested that a dose-dependent effect on the reduction of fish growth induced by CLA supplementation should be carefully considered in intensive aquaculture, although lipid reduction is nutritionally important for fatty liver control in grass carp. Furthermore, our results raise the possibility that the lipid-lowering effects of dietary CLA were modulated by the gene expressions in lipogenesis (such as FAS and ACC), lipoprotein transport (such as LPL), and lipolysis (such as HSL) primarily in the liver, foregut, intraperitoneal fat, and muscle. The activation of transcription factors (such as PPARα, PPARγ, and SREBP-1c) may also be responsible for the lipid-lowering effects of dietary CLA.
AB - Conjugated linoleic acid (CLA) has been shown to decrease body fat and increase lean tissue in mammals. However, limited data is available about the effect of CLA on the lipid content in fish tissue, and the mechanisms underlying the beneficial effects of CLA in fish are unknown. We hypothesized that dietary CLA may induce lipid-lowering effects in grass carp (Ctenopharyngodon idella) tissue, and the fat reduction effect was modulated by the expression of genes involved in the lipid metabolism. A 65-day growth trial was conducted to investigate the effect of CLA on the growth, tissue lipid deposition, and gene expression involved in the lipid metabolism of grass carp. Seven isonitrogenous and isolipidic diets were formulated: 0% CLA (control); 0.5% CLA (CLA0.5); 1% CLA (CLA1); 1.5% CLA (CLA1.5); 2% CLA (CLA2); 2.5% CLA (CLA2.5); and 3% CLA (CLA3).Results showed that only fish fed the CLA3 diet exhibited a significant reduction in feeding rate and specific growth rate than those of fish fed the control diet (P<. 0.05). Significant decreases in the lipid content in the liver, intraperitoneal fat, and muscle were observed in fish fed with 2.5% to 3% CLA, 1.5% to 3% CLA, and 2% to 3% CLA diets, respectively (P<. 0.05), compared to those fed with the control diet. Dose- and tissue-dependent changes were found in the mRNA expressions of fatty acid synthetase (FAS), acetyl-CoA carboxylase (ACC), lipoprotein lipase (LPL), hormone-sensitive lipase (HSL), peroxisome proliferator-activated receptor α (PPARα), peroxisome proliferator-activated receptor γ (PPARγ), and sterol regulatory element binding protein-1c (SREBP-1c). The mRNA expressions in most of the genes examined in the liver, foregut, intraperitoneal fat and muscle were highly sensitive to dietary CLA. Our results suggested that a dose-dependent effect on the reduction of fish growth induced by CLA supplementation should be carefully considered in intensive aquaculture, although lipid reduction is nutritionally important for fatty liver control in grass carp. Furthermore, our results raise the possibility that the lipid-lowering effects of dietary CLA were modulated by the gene expressions in lipogenesis (such as FAS and ACC), lipoprotein transport (such as LPL), and lipolysis (such as HSL) primarily in the liver, foregut, intraperitoneal fat, and muscle. The activation of transcription factors (such as PPARα, PPARγ, and SREBP-1c) may also be responsible for the lipid-lowering effects of dietary CLA.
KW - Conjugated linoleic acid
KW - Ctenopharyngodon idella
KW - Fatty liver
KW - Gene expression
KW - Lipid deposition
UR - http://www.scopus.com/inward/record.url?scp=84901503238&partnerID=8YFLogxK
U2 - 10.1016/j.aquaculture.2014.05.008
DO - 10.1016/j.aquaculture.2014.05.008
M3 - Article
AN - SCOPUS:84901503238
SN - 0044-8486
VL - 432
SP - 181
EP - 191
JO - Aquaculture
JF - Aquaculture
ER -