Rhodiola pre-conditioning reduces exhaustive exercise-induced myocardial injury of insulin resistant mice

Myocardial injury reduction and recovery under acute cardiac stress are adversely impacted by insulin resistance (IR). We previously demonstrated that Rhodiola improved cardiac anti-stress capacity in mice. Thus, this study focuses on the preventive efficacy of Rhodiola on exhaustive exercise (EE)-i...

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Published inScientific reports Vol. 12; no. 1; pp. 20277 - 9
Main Authors You, Baiyang, Cheng, Jing, Dun, Yaoshan, Ripley-Gonzalez, Jeffrey W., Liu, Jie, Li, Dezhao, Fu, Siqian, Hong, Chuangxiong, Liu, Suixin
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 23.11.2022
Nature Publishing Group
Nature Portfolio
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Summary:Myocardial injury reduction and recovery under acute cardiac stress are adversely impacted by insulin resistance (IR). We previously demonstrated that Rhodiola improved cardiac anti-stress capacity in mice. Thus, this study focuses on the preventive efficacy of Rhodiola on exhaustive exercise (EE)-induced myocardial injury of IR mice. An 8-week high-fat diet (HFD) model of IR mice was established. Rhodiola was administrated by garaging. After the 8-week intervention, half of the mice performed EE to simulate acute cardiac stress, and determine myocardial injury; The remaining mice were sacrificed following fasting to assess metabolic disorder. We found myocardial injury induced by EE in IR mice was worse and was alleviated by Rhodiola pre-conditioning. Further, the nuclear factor erythroid 2-related factor 2 (Nrf2)-related antioxidant system was impaired by HFD, while mitochondrial dynamic fusion and fission were activated by HFD as a physiological protective compensation. The Rhodiola administration rescued Nrf2 impairment and further facilitated mitochondrial fusion and fission. All these results indicate that Rhodiola is a potential treatment for the prevention of cardiac events in type 2 diabetes mellitus and metabolic syndrome patients, and the Nrf2-related antioxidant activity and mitochondrial dynamics are the proposed mechanisms.
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ISSN:2045-2322
2045-2322
DOI:10.1038/s41598-022-20376-4