Corticosterone-Induced Lipogenesis Activation and Lipophagy Inhibition in Chicken Liver Are Alleviated by Maternal Betaine Supplementation
We have shown previously that in ovo betaine injection can prevent nonalcoholic fatty liver induced by glucocorticoid exposure in chickens; yet it remains unknown whether feeding betaine to laying hens may exert similar effects in their progeny. In this study, we fed laying hens a betaine-supplement...
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Published in | The Journal of nutrition Vol. 148; no. 3; pp. 316 - 325 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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United States
Elsevier Inc
01.03.2018
American Institute of Nutrition |
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Abstract | We have shown previously that in ovo betaine injection can prevent nonalcoholic fatty liver induced by glucocorticoid exposure in chickens; yet it remains unknown whether feeding betaine to laying hens may exert similar effects in their progeny.
In this study, we fed laying hens a betaine-supplemented diet, and the progeny were later exposed chronically to corticosterone (CORT) to test hepatoprotective effects and further elucidate underlying mechanisms.
Rugao yellow-feathered laying hens (n = 120) were fed a basal (control, C) diet or a 0.5% betaine-supplemented (B) diet for 28 d before their eggs were collected for incubation. At 49 d of age, male chickens selected from each group were daily injected subcutaneously with solvent (15% ethanol; vehicle, VEH) or CORT (4.0 mg/kg body mass) for 7 d to establish a fatty liver model. Chickens in the 4 groups (C-VEH, C-CORT, B-VEH, and B-CORT) were killed at day 57. Plasma and hepatic triglyceride (TG) concentrations, as well as the hepatic expression of genes involved in lipogenesis and lipophagy, were determined.
CORT induced a 1.6-fold increase in the plasma TG concentration (P < 0.05) and a 1.8-fold increment in the hepatic TG concentration (P < 0.05), associated with activation of lipogenic genes (70–780%). In contrast, lipophagy and mitochondrial β-oxidation genes were inhibited by 30–60% (P < 0.05) in CORT-treated chickens. These CORT-induced changes were completely normalized by maternal betaine supplementation or were partially normalized to intermediate values that were significantly different from those in the C-VEH and C-CORT groups. These effects were accompanied by modifications in CpG methylation and glucocorticoid receptor binding to the promoters of major lipogenic and lipophagic genes (P < 0.05).
These results indicate that maternal betaine supplementation protects male juvenile chickens from CORT-induced TG accumulation in the liver via epigenetic modulation of lipogenic and lipophagic genes. |
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AbstractList | We have shown previously that in ovo betaine injection can prevent nonalcoholic fatty liver induced by glucocorticoid exposure in chickens; yet it remains unknown whether feeding betaine to laying hens may exert similar effects in their progeny.
In this study, we fed laying hens a betaine-supplemented diet, and the progeny were later exposed chronically to corticosterone (CORT) to test hepatoprotective effects and further elucidate underlying mechanisms.
Rugao yellow-feathered laying hens (n = 120) were fed a basal (control, C) diet or a 0.5% betaine-supplemented (B) diet for 28 d before their eggs were collected for incubation. At 49 d of age, male chickens selected from each group were daily injected subcutaneously with solvent (15% ethanol; vehicle, VEH) or CORT (4.0 mg/kg body mass) for 7 d to establish a fatty liver model. Chickens in the 4 groups (C-VEH, C-CORT, B-VEH, and B-CORT) were killed at day 57. Plasma and hepatic triglyceride (TG) concentrations, as well as the hepatic expression of genes involved in lipogenesis and lipophagy, were determined.
CORT induced a 1.6-fold increase in the plasma TG concentration (P < 0.05) and a 1.8-fold increment in the hepatic TG concentration (P < 0.05), associated with activation of lipogenic genes (70–780%). In contrast, lipophagy and mitochondrial β-oxidation genes were inhibited by 30–60% (P < 0.05) in CORT-treated chickens. These CORT-induced changes were completely normalized by maternal betaine supplementation or were partially normalized to intermediate values that were significantly different from those in the C-VEH and C-CORT groups. These effects were accompanied by modifications in CpG methylation and glucocorticoid receptor binding to the promoters of major lipogenic and lipophagic genes (P < 0.05).
These results indicate that maternal betaine supplementation protects male juvenile chickens from CORT-induced TG accumulation in the liver via epigenetic modulation of lipogenic and lipophagic genes. We have shown previously that in ovo betaine injection can prevent nonalcoholic fatty liver induced by glucocorticoid exposure in chickens; yet it remains unknown whether feeding betaine to laying hens may exert similar effects in their progeny. In this study, we fed laying hens a betaine-supplemented diet, and the progeny were later exposed chronically to corticosterone (CORT) to test hepatoprotective effects and further elucidate underlying mechanisms. Rugao yellow-feathered laying hens (n = 120) were fed a basal (control, C) diet or a 0.5% betaine-supplemented (B) diet for 28 d before their eggs were collected for incubation. At 49 d of age, male chickens selected from each group were daily injected subcutaneously with solvent (15% ethanol; vehicle, VEH) or CORT (4.0 mg/kg body mass) for 7 d to establish a fatty liver model. Chickens in the 4 groups (C-VEH, C-CORT, B-VEH, and B-CORT) were killed at day 57. Plasma and hepatic triglyceride (TG) concentrations, as well as the hepatic expression of genes involved in lipogenesis and lipophagy, were determined. CORT induced a 1.6-fold increase in the plasma TG concentration (P < 0.05) and a 1.8-fold increment in the hepatic TG concentration (P < 0.05), associated with activation of lipogenic genes (70-780%). In contrast, lipophagy and mitochondrial β-oxidation genes were inhibited by 30-60% (P < 0.05) in CORT-treated chickens. These CORT-induced changes were completely normalized by maternal betaine supplementation or were partially normalized to intermediate values that were significantly different from those in the C-VEH and C-CORT groups. These effects were accompanied by modifications in CpG methylation and glucocorticoid receptor binding to the promoters of major lipogenic and lipophagic genes (P < 0.05). These results indicate that maternal betaine supplementation protects male juvenile chickens from CORT-induced TG accumulation in the liver via epigenetic modulation of lipogenic and lipophagic genes. |
Author | Hu, Yun Zhao, Ruqian Hou, Zhen Hu, Yan Sun, Qinwei Omer, Nagmeldin A Zong, Yibo Abobaker, Halima |
Author_xml | – sequence: 1 givenname: Yun surname: Hu fullname: Hu, Yun organization: MOE Joint International Research Laboratory of Animal Health & Food Safety – sequence: 2 givenname: Qinwei surname: Sun fullname: Sun, Qinwei organization: MOE Joint International Research Laboratory of Animal Health & Food Safety – sequence: 3 givenname: Yan surname: Hu fullname: Hu, Yan organization: Poultry Institute, Chinese Academy of Agriculture Science, Yangzhou, Jiangsu, China – sequence: 4 givenname: Zhen surname: Hou fullname: Hou, Zhen organization: MOE Joint International Research Laboratory of Animal Health & Food Safety – sequence: 5 givenname: Yibo surname: Zong fullname: Zong, Yibo organization: MOE Joint International Research Laboratory of Animal Health & Food Safety – sequence: 6 givenname: Nagmeldin A surname: Omer fullname: Omer, Nagmeldin A organization: MOE Joint International Research Laboratory of Animal Health & Food Safety – sequence: 7 givenname: Halima surname: Abobaker fullname: Abobaker, Halima organization: MOE Joint International Research Laboratory of Animal Health & Food Safety – sequence: 8 givenname: Ruqian surname: Zhao fullname: Zhao, Ruqian email: zhao.ruqian@gmail.com organization: MOE Joint International Research Laboratory of Animal Health & Food Safety |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29546310$$D View this record in MEDLINE/PubMed |
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Keywords | B NAFLD C mtDNA fatty liver lipogenesis ChIP epigenetic regulation ACACA HSD11B2 LAMP1 ATG7 MeDIP SREBF1 CPT1A lipophagy GR MAP1LC3 CORT HSD11B1a SCD FASN VEH TFAM GRE betaine corticosterone |
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Snippet | We have shown previously that in ovo betaine injection can prevent nonalcoholic fatty liver induced by glucocorticoid exposure in chickens; yet it remains... |
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SubjectTerms | Animals Betaine Betaine - pharmacology Betaine - therapeutic use Body mass Chickens Corticosterone Corticosterone - adverse effects Corticosterone - metabolism Diet Dietary Supplements Disease Models, Animal DNA methylation DNA Methylation - drug effects Eggs Epigenesis, Genetic epigenetic regulation Ethanol Fatty liver Fatty Liver - etiology Fatty Liver - metabolism Fatty Liver - prevention & control Female Gene expression Genes Incubation Lipid Metabolism - drug effects Lipid Metabolism - genetics Lipogenesis Lipogenesis - drug effects Lipogenesis - genetics lipophagy Liver Liver - drug effects Liver - metabolism Male Mitochondria Mitochondrial Proteins - genetics Offspring Oxidation Poultry Pregnancy Prenatal Nutritional Physiological Phenomena Progeny Promoter Regions, Genetic Receptors, Glucocorticoid - metabolism Transcription activation Triglycerides - metabolism |
Title | Corticosterone-Induced Lipogenesis Activation and Lipophagy Inhibition in Chicken Liver Are Alleviated by Maternal Betaine Supplementation |
URI | https://dx.doi.org/10.1093/jn/nxx073 https://www.ncbi.nlm.nih.gov/pubmed/29546310 https://www.proquest.com/docview/2035253231 |
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