1. Academic Validation
  2. Resveratrol as a new inhibitor of immunoproteasome prevents PTEN degradation and attenuates cardiac hypertrophy after pressure overload

Resveratrol as a new inhibitor of immunoproteasome prevents PTEN degradation and attenuates cardiac hypertrophy after pressure overload

  • Redox Biol. 2019 Jan;20:390-401. doi: 10.1016/j.redox.2018.10.021.
Chen Chen 1 Lei-Xin Zou 1 Qiu-Yue Lin 2 Xiao Yan 1 Hai-Lian Bi 2 Xin Xie 2 Shuai Wang 3 Qing-Shan Wang 1 Yun-Long Zhang 4 Hui-Hua Li 5
Affiliations

Affiliations

  • 1 Department of Nutrition and Food Hygiene, School of Public Health, Dalian Medical University, Dalian 116044, China.
  • 2 Department of Cardiology, Institute of Cardiovascular Diseases, First Affiliated Hospital of Dalian Medical University, Dalian 116011, China.
  • 3 Department of Ophthalmology, Second Affiliated Hospital of Dalian Medical University, Dalian 116023, China.
  • 4 Department of Nutrition and Food Hygiene, School of Public Health, Dalian Medical University, Dalian 116044, China; Department of Cardiology, Institute of Cardiovascular Diseases, First Affiliated Hospital of Dalian Medical University, Dalian 116011, China. Electronic address: 674250228@qq.com.
  • 5 Department of Nutrition and Food Hygiene, School of Public Health, Dalian Medical University, Dalian 116044, China; Department of Cardiology, Institute of Cardiovascular Diseases, First Affiliated Hospital of Dalian Medical University, Dalian 116011, China. Electronic address: hhli1935@aliyun.com.
Abstract

Sustained cardiac hypertrophy is a major cause of heart failure (HF) and death. Recent studies have demonstrated that resveratrol (RES) exerts a protective role in hypertrophic diseases. However, the molecular mechanisms involved are not fully elucidated. In this study, cardiac hypertrophic remodeling in mice were established by pressure overload induced by transverse aortic constriction (TAC). Cardiac function was evaluated by echocardiography and invasive pressure-volume analysis. Cardiomyocyte size was detected by wheat germ agglutinin staining. The protein and gene expressions of signaling mediators and hypertrophic markers were examined. Our results showed that administration of RES significantly suppressed pressure overload-induced cardiac hypertrophy, fibrosis and Apoptosis and improved in vivo heart function in mice. RES also reversed pre-established hypertrophy and restoring contractile dysfunction induced by chronic pressure overload. Moreover, RES treatment blocked TAC-induced increase of immunoproteasome activity and catalytic subunit expression (β1i, β2i and β5i), which inhibited PTEN degradation thereby leading to inactivation of Akt/mTOR and activation of AMPK signals. Further, blocking PTEN by the specific inhibitor VO-Ohpic significantly attenuated RES inhibitory effect on cardiomyocyte hypertrophy in vivo and in vitro. Taken together, our data suggest that RES is a novel inhibitor of immunoproteasome activity, and may represent a promising therapeutic agent for the treatment of hypertrophic diseases.

Keywords

AKT/mTOR; AMPK; Cardiac hypertrophy; Immunoproteasome; PTEN degradation; Resveratrol.

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