Effect of combined supplementation with vitamin E and alpha-lipoic acid on myocardial performance during in vivo ischaemia-reperfusion

Acta Physiol Scand. 2000 Aug;169(4):261-9. doi: 10.1046/j.1365-201x.2000.00740.x.

Abstract

Reactive oxygen species (ROS) contribute significantly to myocardial ischaemia-reperfusion (I-R) injury. Recently the combination of the antioxidants vitamin E (VE) and alpha-lipoic acid (alpha-LA) has been reported to improve cardiac performance and reduce myocardial lipid peroxidation during in vitro I-R. The purpose of these experiments was to investigate the effects of VE and alpha-LA supplementation on cardiac performance, incidence of dysrhythmias and biochemical alterations during an in vivo myocardial I-R insult. Female Sprague-Dawley rats (4-months old) were assigned to one of the two dietary treatments: (1) control diet (CON) or (2) VE and alpha-LA supplementation (ANTIOXID). The CON diet was prepared to meet AIN-93M standards, which contains 75 IU VE kg-1 diet. The ANTIOXID diet contained 10 000 IU VE kg(-1) diet and 1.65 g alpha-LA kg(-1) diet. After the 14-week feeding period, significant differences (P<0.05) existed in mean myocardial VE levels between dietary groups. Animals in each experimental group were subjected to an in vivo I-R protocol which included 25 min of left anterior coronary artery occlusion followed by 10 min of reperfusion. No group differences (P>0.05) existed in cardiac performance (e.g. peak arterial pressure or ventricular work) or the incidence of ventricular dysrhythmias during the I-R protocol. Following I-R, two markers of lipid peroxidation were lower (P<0.05) in the ANTIOXID animals compared with CON. These data indicate that dietary supplementation of the antioxidants, VE and alpha-LA do not influence cardiac performance or the incidence of dysrhythmias but do decrease lipid peroxidation during in vivo I-R in young adult rats.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants / pharmacology*
  • Benzene Derivatives / metabolism
  • Blood Pressure / drug effects
  • Dietary Supplements*
  • Disease Models, Animal
  • Female
  • Free Radicals / metabolism
  • Heart / physiopathology
  • Lipid Peroxidation / drug effects
  • Myocardial Contraction / drug effects*
  • Myocardial Reperfusion Injury / diet therapy*
  • Myocardial Reperfusion Injury / metabolism
  • Myocardial Reperfusion Injury / physiopathology
  • Random Allocation
  • Rats
  • Rats, Sprague-Dawley
  • Sulfhydryl Compounds / metabolism
  • Thiobarbituric Acid Reactive Substances / metabolism
  • Thioctic Acid / pharmacology*
  • Ventricular Function / drug effects
  • Vitamin E / pharmacology*

Substances

  • Antioxidants
  • Benzene Derivatives
  • Free Radicals
  • Sulfhydryl Compounds
  • Thiobarbituric Acid Reactive Substances
  • Vitamin E
  • Thioctic Acid
  • cumene hydroperoxide