Literature DB >> 25451966

Preclinical and clinical evidence for the role of resveratrol in the treatment of cardiovascular diseases.

Beshay N M Zordoky1, Ian M Robertson1, Jason R B Dyck2.   

Abstract

Cardiovascular disease is the leading cause of death worldwide. Despite advancements in diagnosis and treatment of cardiovascular disease, the incidence of cardiovascular disease is still rising. Therefore, new lines of medications are needed to treat the growing population of patients with cardiovascular disease. Although the majority of the existing pharmacotherapies for cardiovascular disease are synthesized molecules, natural compounds, such as resveratrol, are also being tested. Resveratrol is a non-flavonoid polyphenolic compound, which has several biological effects. Preclinical studies have provided convincing evidence that resveratrol has beneficial effects in animal models of hypertension, atherosclerosis, stroke, ischemic heart disease, arrhythmia, chemotherapy-induced cardiotoxicity, diabetic cardiomyopathy, and heart failure. Although not fully delineated, some of the beneficial cardiovascular effects of resveratrol are mediated through activation of silent information regulator 1 (SIRT1), AMP-activated protein kinase (AMPK), and endogenous anti-oxidant enzymes. In addition to these pathways, the anti-inflammatory, anti-platelet, insulin-sensitizing, and lipid-lowering properties of resveratrol contribute to its beneficial cardiovascular effects. Despite the promise of resveratrol as a treatment for numerous cardiovascular diseases, the clinical studies for resveratrol are still limited. In addition, several conflicting results from trials have been reported, which demonstrates the challenges that face the translation of the exciting preclinical findings to humans. Herein, we will review much of the preclinical and clinical evidence for the role of resveratrol in the treatment of cardiovascular disease and provide information about the physiological and molecular signaling mechanisms involved. This article is part of a Special Issue entitled: Resveratrol: Challenges in translating pre-clinical findings to improved patient outcomes.
Copyright © 2014 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Cardiovascular disease; Resveratrol

Mesh:

Substances:

Year:  2014        PMID: 25451966     DOI: 10.1016/j.bbadis.2014.10.016

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  90 in total

1.  Resveratrol attenuated estrogen-deficient-induced cardiac dysfunction: role of AMPK, SIRT1, and mitochondrial function.

Authors:  Zijun Meng; Hongjiang Jing; Lu Gan; Hua Li; Bingde Luo
Journal:  Am J Transl Res       Date:  2016-06-15       Impact factor: 4.060

Review 2.  Antioxidant effects of resveratrol in the cardiovascular system.

Authors:  Ning Xia; Andreas Daiber; Ulrich Förstermann; Huige Li
Journal:  Br J Pharmacol       Date:  2016-05-06       Impact factor: 8.739

3.  Effect of resveratrol on metabolic and cardiovascular function in male and female adult offspring exposed to prenatal hypoxia and a high-fat diet.

Authors:  Amin Shah; Laura M Reyes; Jude S Morton; David Fung; Jillian Schneider; Sandra T Davidge
Journal:  J Physiol       Date:  2015-11-04       Impact factor: 5.182

4.  Anticancer effects of resveratrol in canine hemangiosarcoma cell lines.

Authors:  A Carlson; K S Alderete; M K O Grant; D M Seelig; L C Sharkey; B N M Zordoky
Journal:  Vet Comp Oncol       Date:  2017-12-13       Impact factor: 2.613

Review 5.  Contribution of mitochondrial oxidative stress to hypertension.

Authors:  Sergey I Dikalov; Anna E Dikalova
Journal:  Curr Opin Nephrol Hypertens       Date:  2016-03       Impact factor: 2.894

Review 6.  Pharmacological basis and new insights of resveratrol action in the cardiovascular system.

Authors:  Chak Kwong Cheng; Jiang-Yun Luo; Chi Wai Lau; Zhen-Yu Chen; Xiao Yu Tian; Yu Huang
Journal:  Br J Pharmacol       Date:  2019-12-08       Impact factor: 8.739

7.  Activation of AMPK in Human Placental Explants Impairs Mitochondrial Function and Cellular Metabolism.

Authors:  Daphne Landau; Maricela Haghiac; Judi Minium; Yelenna Skomorovska-Prokvolit; Virtu Calabuig-Navarro; Perrie O'Tierney-Ginn
Journal:  Reprod Sci       Date:  2018-05-22       Impact factor: 3.060

8.  Co-administration of resveratrol with doxorubicin in young mice attenuates detrimental late-occurring cardiovascular changes.

Authors:  Nobutoshi Matsumura; Beshay N Zordoky; Ian M Robertson; Shereen M Hamza; Nirmal Parajuli; Carrie-Lynn M Soltys; Donna L Beker; Marianne K Grant; Maria Razzoli; Alessandro Bartolomucci; Jason R B Dyck
Journal:  Cardiovasc Res       Date:  2018-08-01       Impact factor: 10.787

9.  Quantitative and systems pharmacology 4. Network-based analysis of drug pleiotropy on coronary artery disease.

Authors:  Jiansong Fang; Chuipu Cai; Yanting Chai; Jingwei Zhou; Yujie Huang; Li Gao; Qi Wang; Feixiong Cheng
Journal:  Eur J Med Chem       Date:  2018-10-15       Impact factor: 6.514

10.  Resveratrol pretreatment alleviates myocardial ischemia/reperfusion injury by inhibiting STIM1-mediated intracellular calcium accumulation.

Authors:  Han Xu; Jing Cheng; Xianbao Wang; Haiqiong Liu; Siyi Wang; Jixiong Wu; Banglong Xu; Aihua Chen; Fei He
Journal:  J Physiol Biochem       Date:  2019-11-30       Impact factor: 4.158

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