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In ovo injection of betaine alleviates corticosterone-induced fatty liver in chickens through epigenetic modifications
Betaine alleviates high-fat diet-induced fatty liver and prenatal betaine programs offspring hepatic lipid metabolism. Excessive corticosterone (CORT) exposure causes fatty liver in chickens, yet it remains unknown whether and how prenatal betaine modulates the susceptibility of CORT-induced fatty l...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5216338/ https://www.ncbi.nlm.nih.gov/pubmed/28059170 http://dx.doi.org/10.1038/srep40251 |
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author | Hu, Yun Sun, Qinwei Liu, Jie Jia, Yimin Cai, Demin Idriss, Abdulrahman A. Omer, Nagmeldin A. Zhao, Ruqian |
author_facet | Hu, Yun Sun, Qinwei Liu, Jie Jia, Yimin Cai, Demin Idriss, Abdulrahman A. Omer, Nagmeldin A. Zhao, Ruqian |
author_sort | Hu, Yun |
collection | PubMed |
description | Betaine alleviates high-fat diet-induced fatty liver and prenatal betaine programs offspring hepatic lipid metabolism. Excessive corticosterone (CORT) exposure causes fatty liver in chickens, yet it remains unknown whether and how prenatal betaine modulates the susceptibility of CORT-induced fatty liver later in life. In this study, fertilized eggs were injected with saline or betaine before incubation, and the hatchlings were raised at 8 weeks of age followed by 7 days of subcutaneous CORT injection. CORT-induced fatty liver was less severe in betaine-treated chickens, with significantly reduced oil-red staining and hepatic triglyceride content (P < 0.05). The protective effect of prenatal betaine was associated with significantly up-regulated expression of PPARα and CPT1α, as well as mitochondrial DNA (mtDNA)-encoded genes (P < 0.05). Moreover, betaine rescued CORT-induced alterations in methionine cycle genes, which coincided with modifications of CpG methylation on CPT1α gene promoter and mtDNA D-loop regions. Furthermore, the elevation of hepatic GR protein content after CORT treatment was significantly reduced (P < 0.05), while the reduction of GR binding to the control region of affected genes was significantly increased (P < 0.05), in betaine-treated chickens. These results indicate that in ovo betaine injection protects the juvenile chickens from CORT-induced fatty liver. |
format | Online Article Text |
id | pubmed-5216338 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-52163382017-01-09 In ovo injection of betaine alleviates corticosterone-induced fatty liver in chickens through epigenetic modifications Hu, Yun Sun, Qinwei Liu, Jie Jia, Yimin Cai, Demin Idriss, Abdulrahman A. Omer, Nagmeldin A. Zhao, Ruqian Sci Rep Article Betaine alleviates high-fat diet-induced fatty liver and prenatal betaine programs offspring hepatic lipid metabolism. Excessive corticosterone (CORT) exposure causes fatty liver in chickens, yet it remains unknown whether and how prenatal betaine modulates the susceptibility of CORT-induced fatty liver later in life. In this study, fertilized eggs were injected with saline or betaine before incubation, and the hatchlings were raised at 8 weeks of age followed by 7 days of subcutaneous CORT injection. CORT-induced fatty liver was less severe in betaine-treated chickens, with significantly reduced oil-red staining and hepatic triglyceride content (P < 0.05). The protective effect of prenatal betaine was associated with significantly up-regulated expression of PPARα and CPT1α, as well as mitochondrial DNA (mtDNA)-encoded genes (P < 0.05). Moreover, betaine rescued CORT-induced alterations in methionine cycle genes, which coincided with modifications of CpG methylation on CPT1α gene promoter and mtDNA D-loop regions. Furthermore, the elevation of hepatic GR protein content after CORT treatment was significantly reduced (P < 0.05), while the reduction of GR binding to the control region of affected genes was significantly increased (P < 0.05), in betaine-treated chickens. These results indicate that in ovo betaine injection protects the juvenile chickens from CORT-induced fatty liver. Nature Publishing Group 2017-01-06 /pmc/articles/PMC5216338/ /pubmed/28059170 http://dx.doi.org/10.1038/srep40251 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Hu, Yun Sun, Qinwei Liu, Jie Jia, Yimin Cai, Demin Idriss, Abdulrahman A. Omer, Nagmeldin A. Zhao, Ruqian In ovo injection of betaine alleviates corticosterone-induced fatty liver in chickens through epigenetic modifications |
title | In ovo injection of betaine alleviates corticosterone-induced fatty liver in chickens through epigenetic modifications |
title_full | In ovo injection of betaine alleviates corticosterone-induced fatty liver in chickens through epigenetic modifications |
title_fullStr | In ovo injection of betaine alleviates corticosterone-induced fatty liver in chickens through epigenetic modifications |
title_full_unstemmed | In ovo injection of betaine alleviates corticosterone-induced fatty liver in chickens through epigenetic modifications |
title_short | In ovo injection of betaine alleviates corticosterone-induced fatty liver in chickens through epigenetic modifications |
title_sort | in ovo injection of betaine alleviates corticosterone-induced fatty liver in chickens through epigenetic modifications |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5216338/ https://www.ncbi.nlm.nih.gov/pubmed/28059170 http://dx.doi.org/10.1038/srep40251 |
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