Document 0468 DOCN M9550468 TI Alpha-lipoic acid increases intracellular glutathione in a human T-lymphocyte Jurkat cell line. DT 9505 AU Han D; Tritschler HJ; Packer L; Department of Molecular and Cell Biology, University of; California at Berkeley 94720-3200. SO Biochem Biophys Res Commun. 1995 Feb 6;207(1):258-64. Unique Identifier : AIDSLINE MED/95160683 AB The addition of exogenous alpha-lipoic acid to cellular medium causes a rapid increase of intracellular unbound thiols in Jurkat cells, a human T-lymphocyte cell line. The rise of cellular thiols is a result of the cellular uptake and reduction of lipoic acid to dihydrolipoic acid and a rise in intracellular glutathione. Although the level of dihydrolipoic acid is 100-fold lower than glutathione, the cellular concentration of dihydrolipoic acid might be responsible for the modulation of total cellular thiol levels. Rises in glutathione correlate with the levels of intracellular dihydrolipoic acid (p < .01). This increase in glutathione is not the result of expression of new proteins like gamma-glutamylcysteine synthetase, since the rise in glutathione was not inhibited by cycloheximide, a protein synthesis inhibitor. Lipoic acid administration is therefore a potential therapeutic agent in an array of diseases with glutathione anomalies including HIV infection. DE Cell Line Chromatography, High Pressure Liquid Dose-Response Relationship, Drug Glutathione/*METABOLISM Human Kinetics T-Lymphocytes Thioctic Acid/ANALOGS & DERIVATIVES/ANALYSIS/*PHARMACOLOGY Time Factors Tumor Cells, Cultured JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).