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Interdisciplinary Nutritional Science Program, Department of Kinesiology, University of Wisconsin, Madison, Wisconsin 53706
The present
study examined the effects of oral reduced glutathione (GSH)
supplementation in conjunction with endurance training on contractile
function, antioxidant defense, and oxidative damage in response to
ischemia-reperfusion (I/R) in rat hearts. Female Sprague-Dawley
rats (age 4 mo, n = 72) were randomly assigned to a
treadmill-trained (T; 25 m/min, 15% grade, for 75 min/day, 5 days/wk,
for 10 wk) or untrained (U) group. Each group was further divided into
rats receiving 5 g GSH/kg diet during the final 17 days of
training (GSH-S) and control (C) groups. One-half of each group of rats
was subjected to I/R by surgical occlusion of the main coronary artery
for 45 min, followed by 30-min reperfusion or sham operation. Left
ventriclar (LV) peak systolic pressure (LVSP) and contractility
(+dP/dt), measured with a catheter inserted into the LV via
the carotid artery, decreased with I/R in all groups (P < 0.05). However, LVSP with I/R in the T/GSH-S group was 9.5%, 17%,
and 18% higher (P < 0.05) than that in the U/GSH-S, T/C, and U/C groups, respectively. +dP/dt with I/R was 19%,
27%, and 29% (P < 0.05) greater in the T/GSH-S group
versus the T/C, U/GSH-S, and U/C groups, respectively. I/R decreased
heart GSH content by 12-17% (P < 0.05) and
increased oxidized glutathione (GSSG) by 20-27%
(P < 0.05). T/GSH-S hearts showed 15% higher GSH
(P < 0.05) and a 32% higher GSH-to-GSSG ratio
(P < 0.05) than the U/C group at the end of I/R.
Myocardial superoxide dismutase, GSH peroxidase, glutathione reductase,
and
-glutamyl transpeptidase activities were increased with
treadmill training in both GSH-S and C rats. I/R induced myocardial
lipid peroxidation and lactate dehydrogenase release were attenuated
with T/GSH-S treatment. The present data indicate that training in
conjunction with dietary GSH supplementation can increase myocardial
GSH content and antioxidant defense capacity, thereby protecting the
intact heart against oxidative damage and functional retardation caused
by I/R.
antioxidant; heart; oxidative damage
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