Lipoic acid acutely induces hypoglycemia in fasting nondiabetic and diabetic rats

• Published in: Metabolism, clinical and experimental clinical and experimental, 1999-04, Vol.48 (4), p.504-510
• Main Authors: Khamaisi, Mogher, Rudich, Assaf, Potashnik, Ruth, Tritschler, Hans J., Gutman, Alisa, Bashan, Nava
• Format: Article
• Language: English
• Subjects: 3-Hydroxybutyric Acid - blood; Alanine - blood; Animals; Biological and medical sciences; Blood Glucose - metabolism; Carnitine - blood; Diabetes Mellitus, Experimental - blood; Fasting - blood; Fatty Acids, Nonesterified - blood; Glucagon - pharmacology; Gluconeogenesis - drug effects; Hormones. Endocrine system; Hypoglycemia - blood; Hypoglycemia - chemically induced; Liver - enzymology; Liver - metabolism; Male; Medical sciences; Pharmacology. Drug treatments; Pyruvic Acid - blood; Rats; Rats, Sprague-Dawley; Thioctic Acid - pharmacology; Tropical medicine
• ISSN: 0026-0495; 1532-8600
• DOI: 10.1016/S0026-0495(99)90112-9

Lipoic acid (LA) is a unique antioxidant that increases peripheral glucose utilization in diabetic patients. This study was conducted to investigate whether the inhibition of glucose production could be an additional mechanism for the action of LA. Intravenous (IV) LA injection (100 or 60 mg/kg body weight) to fasting nondiabetic or streptozotocin (STZ)-induced diabetic rats caused a rapid reduction in blood glucose with no effect on circulating insulin levels. In vivo conversion of fructose to glucose was not inhibited by LA, whereas the gluconeogenesis flux from alanine was completely prevented. Reduced liver pyruvate carboxylase (PC) activity in vivo is suggested by the finding that LA induced a decrease in liver coenzyme A (CoA) content (44% and 28% reduction in nondiabetic and diabetic rats, respectively, compared with vehicle-treated animals) and liver acetyl CoA content (80% and 67% reduction in nondiabetic and diabetic rats, respectively). A reduction in plasma free carnitine (42% and 22% in nondiabetic and diabetic rats, respectively) was observed in LA-treated animals, and acylcarnitine levels were increased twofold. This could be attributed to elevated levels of C16 and C18 acylcarnitine, without a detectable accumulation of lipoylcarnitine. Under such conditions, a significant increase in the plasma free fatty acid (FFA) concentration (204% in nondiabetic and 151% in diabetic animals) with no elevation in β-hydroxybutyrate levels was noted. In conclusion, this study suggests that short-term administration of LA at high dosage to normal and diabetic rats causes an inhibition of gluconeogenesis secondary to an interference with hepatic fatty acid oxidation. This may render LA an antihyperglycemic agent for the treatment of diabetic subjects, who display glucose overproduction as a major metabolic abnormality.