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Protective Effect of Jiang Tang Xiao Ke Granules against Skeletal Muscle IR via Activation of the AMPK/SIRT1/PGC-1α Signaling Pathway

The Jiang Tang Xiao Ke (JTXK) granule is a classic Chinese herbal formula that has been put into clinical use in the treatment of type 2 diabetes mellitus for decades. However, whether its ability to ameliorate skeletal muscle insulin resistance (IR) is through modulation of the AMPK/SIRT1/PGC-1α si...

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Autores principales: Bai, Ying, Zuo, Jiacheng, Fang, Xin, Ma, Rufeng, Tian, Tian, Mo, Fangfang, Mu, Qianqian, Zhang, Yi, Yu, Na, Bao, Xueli, Zhang, Dongwei, Gao, Sihua, Zhao, Dandan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8277912/
https://www.ncbi.nlm.nih.gov/pubmed/34326919
http://dx.doi.org/10.1155/2021/5566053
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author Bai, Ying
Zuo, Jiacheng
Fang, Xin
Ma, Rufeng
Tian, Tian
Mo, Fangfang
Mu, Qianqian
Zhang, Yi
Yu, Na
Bao, Xueli
Zhang, Dongwei
Gao, Sihua
Zhao, Dandan
author_facet Bai, Ying
Zuo, Jiacheng
Fang, Xin
Ma, Rufeng
Tian, Tian
Mo, Fangfang
Mu, Qianqian
Zhang, Yi
Yu, Na
Bao, Xueli
Zhang, Dongwei
Gao, Sihua
Zhao, Dandan
author_sort Bai, Ying
collection PubMed
description The Jiang Tang Xiao Ke (JTXK) granule is a classic Chinese herbal formula that has been put into clinical use in the treatment of type 2 diabetes mellitus for decades. However, whether its ability to ameliorate skeletal muscle insulin resistance (IR) is through modulation of the AMPK/SIRT1/PGC-1α signaling pathway remains unknown. Therefore, we aimed to investigate the effects of JTXK granules on IR in skeletal muscle of high-fat diet-induced diabetic mice and C2C12 cells and analyze the underlying mechanisms. In the present study, we showed that JTXK granules attenuated body weight gain, reduced body fat mass, improved body lean mass, and enhanced muscle performance of diabetic mice. JTXK granules also improved glucose metabolism and skeletal muscle insulin sensitivity and partially reversed abnormal serum lipid levels, which might be related to the regulation of the AMPK/SIRT1/PGC-1α pathway, both in skeletal muscle tissue of diabetic mice and in C2C12 cells. Furthermore, drug-containing serum of JTXK granules was capable of enhancing glucose uptake and mitochondrial respiration in C2C12 cells, and AMPKα was proven to be closely involved in this process. Taken together, these results suggest that the JTXK granule ameliorates skeletal muscle IR through activation of the AMPK/SIRT1/PGC-1α signaling pathway, which offers a novel perspective of this formula to combat IR-related metabolic diseases.
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spelling pubmed-82779122021-07-28 Protective Effect of Jiang Tang Xiao Ke Granules against Skeletal Muscle IR via Activation of the AMPK/SIRT1/PGC-1α Signaling Pathway Bai, Ying Zuo, Jiacheng Fang, Xin Ma, Rufeng Tian, Tian Mo, Fangfang Mu, Qianqian Zhang, Yi Yu, Na Bao, Xueli Zhang, Dongwei Gao, Sihua Zhao, Dandan Oxid Med Cell Longev Research Article The Jiang Tang Xiao Ke (JTXK) granule is a classic Chinese herbal formula that has been put into clinical use in the treatment of type 2 diabetes mellitus for decades. However, whether its ability to ameliorate skeletal muscle insulin resistance (IR) is through modulation of the AMPK/SIRT1/PGC-1α signaling pathway remains unknown. Therefore, we aimed to investigate the effects of JTXK granules on IR in skeletal muscle of high-fat diet-induced diabetic mice and C2C12 cells and analyze the underlying mechanisms. In the present study, we showed that JTXK granules attenuated body weight gain, reduced body fat mass, improved body lean mass, and enhanced muscle performance of diabetic mice. JTXK granules also improved glucose metabolism and skeletal muscle insulin sensitivity and partially reversed abnormal serum lipid levels, which might be related to the regulation of the AMPK/SIRT1/PGC-1α pathway, both in skeletal muscle tissue of diabetic mice and in C2C12 cells. Furthermore, drug-containing serum of JTXK granules was capable of enhancing glucose uptake and mitochondrial respiration in C2C12 cells, and AMPKα was proven to be closely involved in this process. Taken together, these results suggest that the JTXK granule ameliorates skeletal muscle IR through activation of the AMPK/SIRT1/PGC-1α signaling pathway, which offers a novel perspective of this formula to combat IR-related metabolic diseases. Hindawi 2021-07-03 /pmc/articles/PMC8277912/ /pubmed/34326919 http://dx.doi.org/10.1155/2021/5566053 Text en Copyright © 2021 Ying Bai et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Bai, Ying
Zuo, Jiacheng
Fang, Xin
Ma, Rufeng
Tian, Tian
Mo, Fangfang
Mu, Qianqian
Zhang, Yi
Yu, Na
Bao, Xueli
Zhang, Dongwei
Gao, Sihua
Zhao, Dandan
Protective Effect of Jiang Tang Xiao Ke Granules against Skeletal Muscle IR via Activation of the AMPK/SIRT1/PGC-1α Signaling Pathway
title Protective Effect of Jiang Tang Xiao Ke Granules against Skeletal Muscle IR via Activation of the AMPK/SIRT1/PGC-1α Signaling Pathway
title_full Protective Effect of Jiang Tang Xiao Ke Granules against Skeletal Muscle IR via Activation of the AMPK/SIRT1/PGC-1α Signaling Pathway
title_fullStr Protective Effect of Jiang Tang Xiao Ke Granules against Skeletal Muscle IR via Activation of the AMPK/SIRT1/PGC-1α Signaling Pathway
title_full_unstemmed Protective Effect of Jiang Tang Xiao Ke Granules against Skeletal Muscle IR via Activation of the AMPK/SIRT1/PGC-1α Signaling Pathway
title_short Protective Effect of Jiang Tang Xiao Ke Granules against Skeletal Muscle IR via Activation of the AMPK/SIRT1/PGC-1α Signaling Pathway
title_sort protective effect of jiang tang xiao ke granules against skeletal muscle ir via activation of the ampk/sirt1/pgc-1α signaling pathway
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8277912/
https://www.ncbi.nlm.nih.gov/pubmed/34326919
http://dx.doi.org/10.1155/2021/5566053
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