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Effects of puerarin on the Akt signaling pathway in bovine preadipocyte differentiation

OBJECTIVE: Puerarin has the potential of regulating the differentiation of preadipocytes, but its mechanism of action has not yet been elucidated. Adipocytes found in adipose tissue, the main endocrine organ, are the main sites of lipid deposition, and are widely used as a cell model in the study of...

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Autores principales: Yun, Jinyan, Yu, Yongsheng, Zhou, Guoli, Luo, Xiaotong, Jin, Haiguo, Zhao, Yumin, Cao, Yang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Asian-Australasian Association of Animal Production Societies (AAAP) and Korean Society of Animal Science and Technology (KSAST) 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6946994/
https://www.ncbi.nlm.nih.gov/pubmed/31208179
http://dx.doi.org/10.5713/ajas.19.0004
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author Yun, Jinyan
Yu, Yongsheng
Zhou, Guoli
Luo, Xiaotong
Jin, Haiguo
Zhao, Yumin
Cao, Yang
author_facet Yun, Jinyan
Yu, Yongsheng
Zhou, Guoli
Luo, Xiaotong
Jin, Haiguo
Zhao, Yumin
Cao, Yang
author_sort Yun, Jinyan
collection PubMed
description OBJECTIVE: Puerarin has the potential of regulating the differentiation of preadipocytes, but its mechanism of action has not yet been elucidated. Adipocytes found in adipose tissue, the main endocrine organ, are the main sites of lipid deposition, and are widely used as a cell model in the study of in vitro fat deposition. This study aimed to investigate the effects of puerarin on adipogenesis in vitro. METHODS: Puerarin was added to the culture medium during the process of adipogenesis. The proliferation and differentiation of bovine preadipocytes was measured through cell viability and staining with oil red O. The content of triacylglycerol was measured using a triglyceride assay kit. The mRNA and protein expression levels of adipogenic genes, peroxisome proliferator-activated receptor-γ (PPARγ) and CCAAT/enhancer-binding protein-α, were measured using quantitative real-time polymerase chain reaction and western blotting, respectively. RESULTS: The addition of puerarin significantly increased adipogenesis of bovine preadipocytes and enhanced the mRNA and protein level expression of PPARγ (p<0.01). The expression of P-Akt increased after adipogenic hormonal induction, whereas puerarin significantly increased PPARγ expression by promoting the Akt signaling component, P-Akt. The mechanism of adipogenesis was found to be related to the phosphorylation level of Ser473, which may activate the downstream signaling of the Akt pathway. CONCLUSION: Puerarin was able to promote the differentiation of preadipocytes and improve fat deposition in cattle. The mechanism of adipogenesis was found to be related to the phosphorylation level of Ser473.
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spelling pubmed-69469942020-01-15 Effects of puerarin on the Akt signaling pathway in bovine preadipocyte differentiation Yun, Jinyan Yu, Yongsheng Zhou, Guoli Luo, Xiaotong Jin, Haiguo Zhao, Yumin Cao, Yang Asian-Australas J Anim Sci Article OBJECTIVE: Puerarin has the potential of regulating the differentiation of preadipocytes, but its mechanism of action has not yet been elucidated. Adipocytes found in adipose tissue, the main endocrine organ, are the main sites of lipid deposition, and are widely used as a cell model in the study of in vitro fat deposition. This study aimed to investigate the effects of puerarin on adipogenesis in vitro. METHODS: Puerarin was added to the culture medium during the process of adipogenesis. The proliferation and differentiation of bovine preadipocytes was measured through cell viability and staining with oil red O. The content of triacylglycerol was measured using a triglyceride assay kit. The mRNA and protein expression levels of adipogenic genes, peroxisome proliferator-activated receptor-γ (PPARγ) and CCAAT/enhancer-binding protein-α, were measured using quantitative real-time polymerase chain reaction and western blotting, respectively. RESULTS: The addition of puerarin significantly increased adipogenesis of bovine preadipocytes and enhanced the mRNA and protein level expression of PPARγ (p<0.01). The expression of P-Akt increased after adipogenic hormonal induction, whereas puerarin significantly increased PPARγ expression by promoting the Akt signaling component, P-Akt. The mechanism of adipogenesis was found to be related to the phosphorylation level of Ser473, which may activate the downstream signaling of the Akt pathway. CONCLUSION: Puerarin was able to promote the differentiation of preadipocytes and improve fat deposition in cattle. The mechanism of adipogenesis was found to be related to the phosphorylation level of Ser473. Asian-Australasian Association of Animal Production Societies (AAAP) and Korean Society of Animal Science and Technology (KSAST) 2020-01 2019-05-28 /pmc/articles/PMC6946994/ /pubmed/31208179 http://dx.doi.org/10.5713/ajas.19.0004 Text en Copyright © 2020 by Asian-Australasian Journal of Animal Sciences This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Yun, Jinyan
Yu, Yongsheng
Zhou, Guoli
Luo, Xiaotong
Jin, Haiguo
Zhao, Yumin
Cao, Yang
Effects of puerarin on the Akt signaling pathway in bovine preadipocyte differentiation
title Effects of puerarin on the Akt signaling pathway in bovine preadipocyte differentiation
title_full Effects of puerarin on the Akt signaling pathway in bovine preadipocyte differentiation
title_fullStr Effects of puerarin on the Akt signaling pathway in bovine preadipocyte differentiation
title_full_unstemmed Effects of puerarin on the Akt signaling pathway in bovine preadipocyte differentiation
title_short Effects of puerarin on the Akt signaling pathway in bovine preadipocyte differentiation
title_sort effects of puerarin on the akt signaling pathway in bovine preadipocyte differentiation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6946994/
https://www.ncbi.nlm.nih.gov/pubmed/31208179
http://dx.doi.org/10.5713/ajas.19.0004
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