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

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作者
Baiyang You
Jing Cheng
Yaoshan Dun
Jeffrey W. Ripley-Gonzalez
Jie Liu
Dezhao Li
Siqian Fu
Chuangxiong Hong
Suixin Liu
机构
[1] Guangzhou University of Chinese Medicine,The First Clinical Medical College
[2] Xiangya Hospital Central South University,Division of Cardiac Rehabilitation, Department of Physical Medicine and Rehabilitation
[3] Shenzhen District Yantian People’s Hospital,Department of Cardiovascular
[4] Xiangya Hospital Central South University,National Clinical Research Center for Geriatric Disorders
[5] Mayo Clinic,Division of Preventive Cardiology, Department of Cardiovascular Medicine
[6] Hunan Traditional Chinese Medical College,Department of Internal Medicine, School of Medicine
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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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