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 inThe Journal of nutrition Vol. 148; no. 3; pp. 316 - 325
Main Authors Hu, Yun, Sun, Qinwei, Hu, Yan, Hou, Zhen, Zong, Yibo, Omer, Nagmeldin A, Abobaker, Halima, Zhao, Ruqian
Format Journal Article
LanguageEnglish
Published 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.
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
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Issue 3
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
Volume 148
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