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Curcumin Prevents High Fat Diet Induced Insulin Resistance and Obesity via Attenuating Lipogenesis in Liver and Inflammatory Pathway in Adipocytes

BACKGROUND: Mechanisms underlying the attenuation of body weight gain and insulin resistance in response to high fat diet (HFD) by the curry compound curcumin need to be further explored. Although the attenuation of the inflammatory pathway is an accepted mechanism, a recent study suggested that cur...

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Autores principales: Shao, Weijuan, Yu, Zhiwen, Chiang, Yuting, Yang, Yi, Chai, Tuanyao, Foltz, Warren, Lu, Huogen, Fantus, I. George, Jin, Tianru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253779/
https://www.ncbi.nlm.nih.gov/pubmed/22253696
http://dx.doi.org/10.1371/journal.pone.0028784
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author Shao, Weijuan
Yu, Zhiwen
Chiang, Yuting
Yang, Yi
Chai, Tuanyao
Foltz, Warren
Lu, Huogen
Fantus, I. George
Jin, Tianru
author_facet Shao, Weijuan
Yu, Zhiwen
Chiang, Yuting
Yang, Yi
Chai, Tuanyao
Foltz, Warren
Lu, Huogen
Fantus, I. George
Jin, Tianru
author_sort Shao, Weijuan
collection PubMed
description BACKGROUND: Mechanisms underlying the attenuation of body weight gain and insulin resistance in response to high fat diet (HFD) by the curry compound curcumin need to be further explored. Although the attenuation of the inflammatory pathway is an accepted mechanism, a recent study suggested that curcumin stimulates Wnt signaling pathway and hence suppresses adipogenic differentiation. This is in contrast with the known repressive effect of curcumin on Wnt signaling in other cell lineages. METHODOLOGY AND PRINCIPAL FINDINGS: We conducted the examination on low fat diet, or HFD fed C57BL/6J mice with or without curcumin intervention for 28 weeks. Curcumin significantly attenuated the effect of HFD on glucose disposal, body weight/fat gain, as well as the development of insulin resistance. No stimulatory effect on Wnt activation was observed in the mature fat tissue. In addition, curcumin did not stimulate Wnt signaling in vitro in primary rat adipocytes. Furthermore, curcumin inhibited lipogenic gene expression in the liver and blocked the effects of HFD on macrophage infiltration and the inflammatory pathway in the adipose tissue. CONCLUSIONS AND SIGNIFICANCE: We conclude that the beneficial effect of curcumin during HFD consumption is mediated by attenuating lipogenic gene expression in the liver and the inflammatory response in the adipose tissue, in the absence of stimulation of Wnt signaling in mature adipocytes.
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spelling pubmed-32537792012-01-17 Curcumin Prevents High Fat Diet Induced Insulin Resistance and Obesity via Attenuating Lipogenesis in Liver and Inflammatory Pathway in Adipocytes Shao, Weijuan Yu, Zhiwen Chiang, Yuting Yang, Yi Chai, Tuanyao Foltz, Warren Lu, Huogen Fantus, I. George Jin, Tianru PLoS One Research Article BACKGROUND: Mechanisms underlying the attenuation of body weight gain and insulin resistance in response to high fat diet (HFD) by the curry compound curcumin need to be further explored. Although the attenuation of the inflammatory pathway is an accepted mechanism, a recent study suggested that curcumin stimulates Wnt signaling pathway and hence suppresses adipogenic differentiation. This is in contrast with the known repressive effect of curcumin on Wnt signaling in other cell lineages. METHODOLOGY AND PRINCIPAL FINDINGS: We conducted the examination on low fat diet, or HFD fed C57BL/6J mice with or without curcumin intervention for 28 weeks. Curcumin significantly attenuated the effect of HFD on glucose disposal, body weight/fat gain, as well as the development of insulin resistance. No stimulatory effect on Wnt activation was observed in the mature fat tissue. In addition, curcumin did not stimulate Wnt signaling in vitro in primary rat adipocytes. Furthermore, curcumin inhibited lipogenic gene expression in the liver and blocked the effects of HFD on macrophage infiltration and the inflammatory pathway in the adipose tissue. CONCLUSIONS AND SIGNIFICANCE: We conclude that the beneficial effect of curcumin during HFD consumption is mediated by attenuating lipogenic gene expression in the liver and the inflammatory response in the adipose tissue, in the absence of stimulation of Wnt signaling in mature adipocytes. Public Library of Science 2012-01-09 /pmc/articles/PMC3253779/ /pubmed/22253696 http://dx.doi.org/10.1371/journal.pone.0028784 Text en Shao et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Shao, Weijuan
Yu, Zhiwen
Chiang, Yuting
Yang, Yi
Chai, Tuanyao
Foltz, Warren
Lu, Huogen
Fantus, I. George
Jin, Tianru
Curcumin Prevents High Fat Diet Induced Insulin Resistance and Obesity via Attenuating Lipogenesis in Liver and Inflammatory Pathway in Adipocytes
title Curcumin Prevents High Fat Diet Induced Insulin Resistance and Obesity via Attenuating Lipogenesis in Liver and Inflammatory Pathway in Adipocytes
title_full Curcumin Prevents High Fat Diet Induced Insulin Resistance and Obesity via Attenuating Lipogenesis in Liver and Inflammatory Pathway in Adipocytes
title_fullStr Curcumin Prevents High Fat Diet Induced Insulin Resistance and Obesity via Attenuating Lipogenesis in Liver and Inflammatory Pathway in Adipocytes
title_full_unstemmed Curcumin Prevents High Fat Diet Induced Insulin Resistance and Obesity via Attenuating Lipogenesis in Liver and Inflammatory Pathway in Adipocytes
title_short Curcumin Prevents High Fat Diet Induced Insulin Resistance and Obesity via Attenuating Lipogenesis in Liver and Inflammatory Pathway in Adipocytes
title_sort curcumin prevents high fat diet induced insulin resistance and obesity via attenuating lipogenesis in liver and inflammatory pathway in adipocytes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253779/
https://www.ncbi.nlm.nih.gov/pubmed/22253696
http://dx.doi.org/10.1371/journal.pone.0028784
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