Literature DB >> 1855672

Therapeutic potential of vitamin E against myocardial ischemic-reperfusion injury.

D R Janero1.   

Abstract

Myocardial ischemia is a disease process characterized by reduced coronary flow such that the supply of nutritive blood to heart muscle (myocardium) is insufficient for normal myocardial aerobic metabolism. Prompt reestablishment of coronary flow by invasive and noninvasive clinical procedures is the most direct and effective means of limiting myocardial damage in ischemic heart disease patients, although reperfusion carries with it an injury component which may reflect, at least to some degree, the toxic effects of partially reduced oxygen species and their participation in degenerative cellular processes such as membrane lipid peroxidation. Vitamin E, a lipophilic, chain-breaking antioxidant, is a prominent membrane constituent in heart muscle, where it modulates/regulates various aspects of heart muscle-cell metabolism and function. Vitamin E's beneficial effects against experimentally induced oxidative damage to the heart, along with inverse epidemiological correlations between plasma vitamin E level and either anginal pain or mortality due to ischemic heart disease, suggest that vitamin E might have protective and therapeutic roles against myocardial ischemic-reperfusion injury. Laboratory investigations aimed at addressing this possibility have demonstrated that vitamin E supplementation protects isolated hearts against ischemic-reperfusion injury, and relatively more inconsistent and limited data document cardioprotective effects of vitamin E in some animal models of myocardial ischemia-reperfusion, especially when administered prior to the ischemic period. Clinical attempts to establish whether vitamin E has therapeutic benefit in ischemic heart disease patients remain inconclusive, having relied upon a variety of nonuniformly controlled protocols and a single, rather subjective endpoint (anginal pain). Consequently, although laboratory data constitute a conceptual context for and indirect support of the idea that vitamin E could be a cardioprotectant against ischemic-reperfusion injury, compelling clinical evidence regarding vitamin E's therapeutic potential in the ischemic heart-disease patient is lacking. Elective coronary revascularization would appear to provide an attractive clinical setting for evaluating the therapeutic efficacy of vitamin E in the context of cardiac ischemia-reperfusion. Further biochemical work would still be required to define how vitamin E exerts any cardioprotective effect observed in these patients.

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Year:  1991        PMID: 1855672     DOI: 10.1016/0891-5849(91)90038-5

Source DB:  PubMed          Journal:  Free Radic Biol Med        ISSN: 0891-5849            Impact factor:   7.376


  10 in total

1.  The effects of a high dose of ascorbate on ischemia-reperfusion-induced mitochondrial dysfunction in canine hearts.

Authors:  Y Nishinaka; S Sugiyama; M Yokota; H Saito; T Ozawa
Journal:  Heart Vessels       Date:  1992       Impact factor: 2.037

2.  Antioxidative vitamin treatment: effect on lipid peroxidation and limb swelling after revascularization operations.

Authors:  H Rabl; G Khoschsorur; W Petek
Journal:  World J Surg       Date:  1995 Sep-Oct       Impact factor: 3.352

3.  Melanoma cell destruction in the microvasculature of perfused hearts is reduced by pretreatment with vitamin E.

Authors:  P A Albertsson; U Nannmark; B R Johansson
Journal:  Clin Exp Metastasis       Date:  1995-07       Impact factor: 5.150

4.  PBN spin trapping of free radicals in the reperfusion-injured heart. Limitations for pharmacological investigations.

Authors:  N Vrbjar; S Zöllner; R F Haseloff; M Pissarek; I E Blasig
Journal:  Mol Cell Biochem       Date:  1998-09       Impact factor: 3.396

5.  Oxidative modulation and inactivation of rabbit cardiac adenylate deaminase.

Authors:  D R Janero; C Yarwood
Journal:  Biochem J       Date:  1995-03-01       Impact factor: 3.857

6.  No evidence of malonyldialdehyde formation during reoxygenation injury in vitamin E-deficient rat heart.

Authors:  C T Marchant; D M Barron; S M Wilson; L R Jordan; R J Willis
Journal:  Basic Res Cardiol       Date:  1993 Jul-Aug       Impact factor: 17.165

Review 7.  Oxidative stress and heart failure.

Authors:  N Singh; A K Dhalla; C Seneviratne; P K Singal
Journal:  Mol Cell Biochem       Date:  1995 Jun 7-21       Impact factor: 3.396

Review 8.  Exosomes in mesenchymal stem cells, a new therapeutic strategy for cardiovascular diseases?

Authors:  Lina Huang; Wenya Ma; Yidi Ma; Dan Feng; Hongyang Chen; Benzhi Cai
Journal:  Int J Biol Sci       Date:  2015-01-12       Impact factor: 6.580

9.  α-Tocopherol preserves cardiac function by reducing oxidative stress and inflammation in ischemia/reperfusion injury.

Authors:  Maria Wallert; Melanie Ziegler; Xiaowei Wang; Ana Maluenda; Xiaoqiu Xu; May Lin Yap; Roman Witt; Corey Giles; Stefan Kluge; Marcus Hortmann; Jianxiang Zhang; Peter Meikle; Stefan Lorkowski; Karlheinz Peter
Journal:  Redox Biol       Date:  2019-08-06       Impact factor: 11.799

10.  In vitro antioxidant effects of barberry fruit extracts.

Authors:  Durdi Qujeq; Solmaz Kamei
Journal:  Int J Mol Cell Med       Date:  2012
  10 in total

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