4.5 Article

Co-ordinated autophagy with resveratrol and γ-tocotrienol confers synergetic cardioprotection

Journal

JOURNAL OF CELLULAR AND MOLECULAR MEDICINE
Volume 14, Issue 10, Pages 2506-2518

Publisher

WILEY
DOI: 10.1111/j.1582-4934.2009.00921.x

Keywords

resveratrol; tocotrienol; autophagy

Funding

  1. National Heart, Lung, and Blood Institute [NIH HL-22559, HL-33889, HL-34360, OTKA 72315, OTKA 78223, TAMOP-4.2.2-08/01-2008-0007]

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This study compared two dietary phytochemicals, grape-derived resveratrol and palm oil-derived gamma-tocotrienol, either alone or in combination, on the contribution of autophagy in cardioprotection during ischaemia and reperfusion. Sprague-Dawley rats weighing between 250 and 300 g were randomly assigned to one of the following groups: vehicle, ischaemia/reperfusion (I/R), resveratrol + I/R, gamma-tocotrienol + I/R, resveratrol + gamma-tocotrienol + I/R. For resveratrol treatments, the rats were gavaged with resveratrol (2.5 mg/kg) for 15 days while for gamma-tocotrienol experiments the rats were gavaged with gamma-tocotrienol (0.3 mg/kg) for 30 days. For the combined resveratrol + gamma-tocotrienol experiments, the rats were gavaged with gamma-tocotrienol for 15 days, and then gavaging continued with resveratrol along with gamma-tocotrienol for a further period of 15 days. After 30 days, isolated perfused hearts were subjected to 30 min. of global ischaemia followed by 2 hrs of reperfusion. Our results showed for the first time that at least in part, the cardioprotection (evidenced from the ventricular performance, myocardial infarct size and cardiomyocyte apoptosis) with resveratrol and gamma-toctrienol was achieved by their abilities to induce autophagy. Most importantly, resveratrol and gamma-tocotrienol acted synergistically providing greater degree of cardioprotection simultaneously generating greater amount of survival signal through the activation of Akt-Bcl-2 survival pathway. Autophagy was accompanied by the activation of Beclin and LC3-II as well as mTOR signalling, which were inhibited by either 3-methyl adenine (3-MA) or Wortmannin. The autophagy was confirmed from the results of transmission electron microscopy and light microscopy as well as with confocal microscopy. It is tempting to speculate that during ischaemia and reperfusion autophagy along with enhanced survival signals helps to recover the cells from injury.

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