Exp Clin Endocrinol Diabetes 2010; 118(1): 61-63
DOI: 10.1055/s-0029-1225649
Article

© J. A. Barth Verlag in Georg Thieme Verlag KG Stuttgart · New York

Chronic Acetonemia Alters Liver Oxidative Balance and Lipid Content in Rats. A Model of Nash?

B. B. de Almeida1 , M. G. Mathias1 , G. V. Portari1 , A. A. Jordao1
  • 1Nutrition and Metabolism Laboratory, Faculty of Medicine of Ribeirao Preto, University of Sao Paulo, Brazil
Further Information

Publication History

received 30.04.2009 first decision 30.04.2009

accepted 10.06.2009

Publication Date:
23 October 2009 (online)

Abstract

Acetone is considered to be a substance that can disturb cellular oxidative status, being also associated with the production of glucose during its metabolization. The objective of the present study was to determine the effects of chronic treatment with acetone in oxidative stress and metabolic parameters in rats. Twenty male Wistar rats were divided into two groups: control (CG) and chronic acetone group (CAG). After 28 days of acetone ingestion in a 5% aqueous solution (CAG) or water (CG) the animals were euthanized and urine, plasma and liver were collected for the determination of acetone, glucose, lipemia, hepatic fat, malondialdehyde (MDA), reduced glutathione (GSH), and vitamin E. As expected, urinary and plasma acetone levels were higher in CAG. There was no difference in hepatic MDA values between groups, whereas hepatic GSH was lower in CAG than in CG and hepatic vitamin E was higher in CAG than in CG. There was also an increase in glycemia, cholesterolemia and hepatic fat in CAG compared to CG. Chronic treatment with a 5% acetone solution produced an increase in acetonemia that was able to promote changes in hepatic oxidative metabolism and in lipid content in rats similar to those observed in nonalcoholic steatohepatitis.

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Correspondence

A. A. Jordao PhD 

Nutrition and Metabolism Laboratory

Faculty of Medicine of Ribeirao Preto

University of Sao Paulo

3900 Av. Bandeirantes

14049-900 Ribeirao Preto/SP

Brazil

Email: alceu@fmrp.usp.br

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