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High-fat diet-induced changes in liver thioredoxin and thioredoxin reductase as a novel feature of insulin resistance

High-fat diet (HFD) can induce oxidative stress. Thioredoxin (Trx) and thioredoxin reductase (TrxR) are critical antioxidant proteins but how they are affected by HFD remains unclear. Using HFD-induced insulin-resistant mouse model, we show here that liver Trx and TrxR are significantly decreased, b...

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Detalles Bibliográficos
Autores principales: Qin, Huijun, Zhang, Xiaolin, Ye, Fei, Zhong, Liangwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4239481/
https://www.ncbi.nlm.nih.gov/pubmed/25426412
http://dx.doi.org/10.1016/j.fob.2014.10.015
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author Qin, Huijun
Zhang, Xiaolin
Ye, Fei
Zhong, Liangwei
author_facet Qin, Huijun
Zhang, Xiaolin
Ye, Fei
Zhong, Liangwei
author_sort Qin, Huijun
collection PubMed
description High-fat diet (HFD) can induce oxidative stress. Thioredoxin (Trx) and thioredoxin reductase (TrxR) are critical antioxidant proteins but how they are affected by HFD remains unclear. Using HFD-induced insulin-resistant mouse model, we show here that liver Trx and TrxR are significantly decreased, but, remarkably, the degree of their S-acylation is increased after consuming HFD. These HFD-induced changes in Trx/TrxR may reflect abnormalities of lipid metabolism and insulin signaling transduction. HFD-driven accumulation of 4-hydroxynonenal is another potential mechanism behind inactivation and decreased expression of Trx/TrxR. Thus, we propose HFD-induced impairment of liver Trx/TrxR as major contributor to oxidative stress and as a novel feature of insulin resistance.
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spelling pubmed-42394812014-11-25 High-fat diet-induced changes in liver thioredoxin and thioredoxin reductase as a novel feature of insulin resistance Qin, Huijun Zhang, Xiaolin Ye, Fei Zhong, Liangwei FEBS Open Bio Article High-fat diet (HFD) can induce oxidative stress. Thioredoxin (Trx) and thioredoxin reductase (TrxR) are critical antioxidant proteins but how they are affected by HFD remains unclear. Using HFD-induced insulin-resistant mouse model, we show here that liver Trx and TrxR are significantly decreased, but, remarkably, the degree of their S-acylation is increased after consuming HFD. These HFD-induced changes in Trx/TrxR may reflect abnormalities of lipid metabolism and insulin signaling transduction. HFD-driven accumulation of 4-hydroxynonenal is another potential mechanism behind inactivation and decreased expression of Trx/TrxR. Thus, we propose HFD-induced impairment of liver Trx/TrxR as major contributor to oxidative stress and as a novel feature of insulin resistance. Elsevier 2014-10-31 /pmc/articles/PMC4239481/ /pubmed/25426412 http://dx.doi.org/10.1016/j.fob.2014.10.015 Text en © 2014 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
spellingShingle Article
Qin, Huijun
Zhang, Xiaolin
Ye, Fei
Zhong, Liangwei
High-fat diet-induced changes in liver thioredoxin and thioredoxin reductase as a novel feature of insulin resistance
title High-fat diet-induced changes in liver thioredoxin and thioredoxin reductase as a novel feature of insulin resistance
title_full High-fat diet-induced changes in liver thioredoxin and thioredoxin reductase as a novel feature of insulin resistance
title_fullStr High-fat diet-induced changes in liver thioredoxin and thioredoxin reductase as a novel feature of insulin resistance
title_full_unstemmed High-fat diet-induced changes in liver thioredoxin and thioredoxin reductase as a novel feature of insulin resistance
title_short High-fat diet-induced changes in liver thioredoxin and thioredoxin reductase as a novel feature of insulin resistance
title_sort high-fat diet-induced changes in liver thioredoxin and thioredoxin reductase as a novel feature of insulin resistance
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4239481/
https://www.ncbi.nlm.nih.gov/pubmed/25426412
http://dx.doi.org/10.1016/j.fob.2014.10.015
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