Diabetes, Vol 48, Issue 10 2045-2051, Copyright © 1999 by American Diabetes Association
Alpha-lipoic acid: effect on glucose uptake, sorbitol pathway, and energy metabolism in experimental diabetic neuropathy
Y Kishi, JD Schmelzer, JK Yao, PJ Zollman, KK Nickander, HJ Tritschler and PA Low
Department of Neurology, Mayo Clinic and Foundation, Rochester, Minnesota 55905, USA.
The peripheral nerve of experimental diabetic neuropathy (EDN) is reported
to be ischemic and hypoxic, with an increased dependence on anaerobic
metabolism, requiring increased energy substrate stores. When glucose
stores become reduced, fiber degeneration has been reported. We evaluated
glucose uptake, nerve energy metabolism, the polyol pathway, and protein
kinase C (PKC) activity in EDN induced by streptozotocin. Control and
diabetic rats received lipoic acid (0, 10, 25, 50, 100 mg/kg). Duration of
diabetes was 1 month, and alpha-lipoic acid was administered
intraperitoneally 5 times per week for the final week of the experiment.
Nerve glucose uptake was reduced to 60, s 37, and 30% of control values in
the sciatic nerve, L5 dorsal root ganglion, and superior cervical ganglion
(SCG), respectively, in rats with EDN. Alpha-lipoic acid supplementation
had no effect on glucose uptake in normal nerves at any dose, but reversed
the deficit in EDN, with a threshold between 10 and 25 mg/kg. Endoneurial
glucose, fructose, sorbitol, and myo-inositol were measured in sciatic
nerve. Alpha-lipoic acid had no significant effect on either energy
metabolism or polyol pathway of normal nerves. In EDN, endoneurial glucose,
fructose, and sorbitol were significantly increased, while myo-inositol was
significantly reduced. Alpha-lipoic acid had a biphasic effect: it
dose-dependently increased fructose, glucose, and sorbitol, peaking at 25
mg/kg, and then fell beyond that dose, and it dose-dependently increased
myo-inositol. Sciatic nerve cytosolic PKC was increased in EDN. ATP,
creatine phosphate, and lactate were measured in sciatic nerve and SCG.
Alpha-lipoic acid prevented the reduction in SCG creatine phosphate. We
conclude that glucose uptake is reduced in EDN and that this deficit is
dose-dependently reversed by alpha-lipoic acid, a change associated with an
improvement in peripheral nerve function.