Diabetes 45:1024-1029, 1996
© 1996 by the American Diabetes Association, Inc.
The antioxidant alpha-lipoic acid enhances insulin-stimulated glucose metabolism in insulin-resistant rat skeletal muscle
ABSTRACT
Insulin resistance of muscle glucose metabolism is a hallmark of NIDDM.
The obese Zucker (fa/fa) rat--an animal model of muscle insulin
resistance--was used to test whether acute (100 mg/kg body wt for 1 h) and
chronic (5-100 mg/kg for 10 days) parenteral treatments with a racemic
mixture of the antioxidant alpha-lipoic acid (ALA) could improve glucose
metabolism in insulin-resistant skeletal muscle. Glucose transport activity
(assessed by net 2-deoxyglucose [2-DG] uptake), net glycogen synthesis, and
glucose oxidation were determined in the isolated epitrochlearis muscles in
the absence or presence of insulin (13.3 nmol/l). Severe insulin resistance
of 2-DG uptake, glycogen synthesis, and glucose oxidation was observed in
muscle from the vehicle-treated obese rats compared with muscle from
vehicle-treated lean (Fa/-) rats. Acute and chronic treatments (30
mg.kg-1.day-1, a maximally effective dose) with ALA significantly (P <
0.05) improved insulin-mediated 2-DG uptake in epitrochlearis muscles from
the obese rats by 62 and 64%, respectively. Chronic ALA treatment increased
both insulin-stimulated glucose oxidation (33%) and glycogen synthesis
(38%) and was associated with a significantly greater (21%) in vivo muscle
glycogen concentration. These adaptive responses after chronic ALA
administration were also associated with significantly lower (15-17%)
plasma levels of insulin and free fatty acids. No significant effects on
glucose transporter (GLUT4) protein level or on the activities of
hexokinase and citrate synthase were observed. Collectively, these findings
indicate that parenteral administration of the antioxidant ALA
significantly enhances the capacity of the insulin-stimulatable glucose
transport system and of both oxidative and nonoxidative pathways of glucose
metabolism in insulin-resistant rat skeletal muscle.

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Copyright © 1996 by the American Diabetes Association.
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