Vol. 297, Issue 2, 516-523, May 2001

Effect of Stavudine on Mitochondrial Genome and Fatty Acid Oxidation in Lean and Obese Mice

Isabelle Gaou, Miriam Malliti, Marie-Christine Guimont, Philippe Lettéron, Christine Demeilliers , Gilles Peytavin, Claude Degott, Dominique Pessayre and Bernard Fromenty

Institut National de la Santé et de la Recherche Médicale Unité 481 and Centre Claude Bernard de Recherches sur les Hépatites Virales (I.G., M.M., P.L., C.D., D.P., B.F.), Service de Biochimie (M.-C.G.), Service Central d'Anatomie et de Cytologie Pathologiques (C.D.), Hôpital Beaujon, Clichy, France; and Pharmacie, Hôpital Bichat, Paris, France (G.P.)

Like other antihuman immunodeficiency virus dideoxynucleosides, stavudine may occasionally induce lactic acidosis and perhaps lipodystrophy in metabolically or genetically susceptible patients. We studied the effects of stavudine on mitochondrial DNA (mtDNA), fatty acid oxidation, and blood metabolites in lean and genetically obese (ob/ob) mice. In lean mice, mtDNA was depleted in liver and skeletal muscle, but not heart and brain, after 6 weeks of stavudine treatment (500 mg/kg/day). With 100 mg/kg/day, mtDNA transiently decreased in liver, but was unchanged at 6 weeks in all organs, including white adipose tissue (WAT). Despite unchanged mtDNA levels, lack of significant oxidative mtDNA lesions (as assessed by long polymerase chain reaction experiments), and normal blood lactate/pyruvate ratios, lean mice treated with stavudine for 6 weeks had increased fasting blood ketone bodies, due to both increased hepatic fatty acid -oxidation and decreased peripheral ketolysis. In obese mice, basal WAT mtDNA was low and was further decreased by stavudine. In conclusion, stavudine can decrease hepatic and muscle mtDNA in lean mice and can also cause ketoacidosis during fasting without altering mtDNA. Stavudine depletes WAT mtDNA only in obese mice. Fasting and ketoacidosis could trigger decompensation in patients with incipient lactic acidosis, whereas WAT mtDNA depletion could cause lipodystrophy in genetically susceptible patients.