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Angiotensin-II-induced Muscle Wasting is Mediated by 25-Hydroxycholesterol via GSK3? Signaling Pathway.


ABSTRACT: While angiotensin II (ang II) has been implicated in the pathogenesis of cardiac cachexia (CC), the molecules that mediate ang II's wasting effect have not been identified. It is known TNF-? level is increased in patients with CC, and TNF-? release is triggered by ang II. We therefore hypothesized that ang II induced muscle wasting is mediated by TNF-?. Ang II infusion led to skeletal muscle wasting in wild type (WT) but not in TNF alpha type 1 receptor knockout (TNFR1KO) mice, suggesting that ang II induced muscle loss is mediated by TNF-? through its type 1 receptor. Microarray analysis identified cholesterol 25-hydroxylase (Ch25h) as the down stream target of TNF-?. Intraperitoneal injection of 25-hydroxycholesterol (25-OHC), the product of Ch25h, resulted in muscle loss in C57BL/6 mice, accompanied by increased expression of atrogin-1, MuRF1 and suppression of IGF-1/Akt signaling pathway. The identification of 25-OHC as an inducer of muscle wasting has implications for the development of specific treatment strategies in preventing muscle loss.

SUBMITTER: Shen C 

PROVIDER: S-EPMC5474518 | biostudies-literature | 2017 Feb

REPOSITORIES: biostudies-literature

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Angiotensin-II-induced Muscle Wasting is Mediated by 25-Hydroxycholesterol via GSK3β Signaling Pathway.

Shen Congcong C   Zhou Jin J   Wang Xiaoxiao X   Yu Xi-Yong XY   Liang Chun C   Liu Bin B   Pan Xiangbin X   Zhao Qiong Q   Song Jenny Lee JL   Wang Jiajun J   Bao Meiyu M   Wu Chaofan C   Li Yangxin Y   Song Yao-Hua YH  

EBioMedicine 20170130


While angiotensin II (ang II) has been implicated in the pathogenesis of cardiac cachexia (CC), the molecules that mediate ang II's wasting effect have not been identified. It is known TNF-α level is increased in patients with CC, and TNF-α release is triggered by ang II. We therefore hypothesized that ang II induced muscle wasting is mediated by TNF-α. Ang II infusion led to skeletal muscle wasting in wild type (WT) but not in TNF alpha type 1 receptor knockout (TNFR1KO) mice, suggesting that a  ...[more]

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