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Lipoic acid prevents liver metabolic changes induced by administration of a fructose-rich diet
Authors:María C Castro  María L Massa  Guillermo Schinella  Juan J Gagliardino  Flavio Francini
Institution:1. CENEXA, Centro de Endocrinología Experimental y Aplicada, UNLP-CONICET LA PLATA, Centro Colaborador OPS/OMS, 1900 La Plata, Argentina;2. Farmacología Básica, Facultad de Ciencias Médicas, 60 y 120, 1900 La Plata, Argentina
Abstract:

Background

To evaluate whether co-administration of R/S-α-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 R/S-α-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 and superoxide dismutase 1 and 2), uncoupling protein 2, PPARδ and PPARγ protein expressions, SREBP-1c, fatty acid synthase and glycerol-3-phosphate acyltransferase-1 gene expression, and glucokinase activity.

Results

R/S-α-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 PPARδ protein expression and increased PPARγ levels, e) restored the basal gene expression of PPARδ, 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.
Keywords:T2DM  type 2 diabetes mellitus  F  fructose-rich diet  ROS  reactive oxygen species  UCP  uncoupling protein  LA  R/S-α-lipoic acid  FAS  fatty acid synthase  GPAT-1  glycerol-3-phosphate acyltransferase-1  HOMA-IR  homeostasis model assessment-insulin resistance  FPI  fasting plasma insulin  FPG  fasting plasma glucose  OGTT  oral glucose tolerance test  AUC  area under the glucose curve  GSH  reduced glutathione  SOD1  superoxide dismutase 1  SOD2  superoxide dismutase 2  ABTS  2  2&prime  -azino-bis-(3-ethylbenzothiazoline-6-sulfonate)
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