CONICET | Buscador de Institutos y Recursos Humanos

Background: To evaluate whether co-administration of á-lipoic acid can prevent the development of oxidative stress and metabolic changes induced by a fructose-rich diet (F). Methods: We assessed glycemia in the fasting state and during an oral glucose tolerance test, triglyceridemia and insulinemia in rats fed with standard diet (control) and fructose without or with á-lipoic acid. Insulin resistance and hepatic insulin sensitivity were also calculated. In liver, we measured reduced glutathione, protein carbonyl groups, antioxidant capacity by ABTS assay, antioxidant enzymes (catalase, superoxide dismutase 1 and 2), uncoupling protein 2, PPARä and PPARã protein expression, SREBP-1c, fatty acid synthase and glycerol-3-phosphate acyltransferase gene expression, and glucokinase activity. Results: á-lipoic acid co-administration to F-fed rats a) prevented hyperinsulinemia, hypertriglyceridemia and insulin resistance, b) improved hepatic insulin sensitivity and glucose tolerance, c) decreased liver oxidative stress and increased antioxidant capacity and antioxidant enzymes expression, d) decreased uncoupling protein 2 and PPARä protein expression and increased PPARã levels, e) restored the basal gene expression of PPARä, SREBP-1c and the lipogenic genes fatty acid synthase and glycerol-3-phosphate acyltransferase, and f) decreased the fructose-mediated enhancement of glucokinase activity . Conclusions: Our results suggest that fructose-induced oxidative stress is an early phenomenon associated with compensatory hepatic metabolic mechanisms, and that treatment with an antioxidant prevented the development of such changes. General Significance: This knowledge would help to better understand the mechanisms involved in liver adaptation to fructose-induced oxidative stress and to develop effective strategies to prevent and treat, at early stages, obesity and type 2 diabetes mellitus.