Glutathione depletion in HIV-infected patients: role of cysteine deficiency and effect of oral N-acetylcysteine
- PMID: 1418777
Glutathione depletion in HIV-infected patients: role of cysteine deficiency and effect of oral N-acetylcysteine
Abstract
Objective: To determine whether a single oral dose of N-acetylcysteine corrects the deficiency of cysteine and glutathione in plasma and mononuclear cells of HIV-infected patients.
Design: Pharmacokinetic and pharmacodynamic study.
Methods: Cysteine and glutathione were measured in plasma and peripheral blood mononuclear cells of patients at different stages of HIV infection before and after a single oral dose of N-acetylcysteine.
Results: At baseline, the plasma concentrations of glutathione and cysteine were significantly lower in HIV-infected patients than in healthy controls. The intracellular concentration of glutathione correlated with the absolute CD4 lymphocyte counts: the concentration of glutathione in mononuclear cells was significantly lower in patients with more advanced immunodeficiency. A single oral dose of N-acetylcysteine increased the concentration of cysteine in plasma and mononuclear cells of HIV-infected patients. Four hours after N-acetylcysteine administration, intracellular glutathione concentrations in the patients were moderately higher than at baseline and at 2 h.
Conclusions: Oral N-acetylcysteine transiently increases the concentrations of cysteine and glutathione in mononuclear cells of patients with HIV infection. A sustained increase in intracellular cysteine may be necessary to normalize intracellular glutathione. This may be accomplished by repeat administration of N-acetylcysteine.
Similar articles
-
Distribution of radio-labeled N-Acetyl-L-Cysteine in Sprague-Dawley rats and its effect on glutathione metabolism following single and repeat dosing by oral gavage.Cutan Ocul Toxicol. 2007;26(2):113-34. doi: 10.1080/15569520701212233. Cutan Ocul Toxicol. 2007. PMID: 17612979
-
Effect of glutathione depletion and oral N-acetyl-cysteine treatment on CD4+ and CD8+ cells.FASEB J. 1994 Apr 1;8(6):448-51. FASEB J. 1994. PMID: 7909525 Clinical Trial.
-
HIV-induced cysteine deficiency and T-cell dysfunction--a rationale for treatment with N-acetylcysteine.Immunol Today. 1992 Jun;13(6):211-4. doi: 10.1016/0167-5699(92)90156-2. Immunol Today. 1992. PMID: 1378279 Review.
-
Effect of oral and intravenous S,N-diacetylcysteine monoethyl ester on circulating and hepatic sulfhydryls in the Rat.J Pharmacol Exp Ther. 2000 Jul;294(1):155-9. J Pharmacol Exp Ther. 2000. PMID: 10871307
-
Cysteine and glutathione deficiency in AIDS patients: a rationale for the treatment with N-acetyl-cysteine.Pharmacology. 1993;46(2):61-5. doi: 10.1159/000139029. Pharmacology. 1993. PMID: 8441757 Review.
Cited by
-
GPX4 regulates cellular necrosis and host resistance in Mycobacterium tuberculosis infection.J Exp Med. 2022 Nov 7;219(11):e20220504. doi: 10.1084/jem.20220504. Epub 2022 Sep 7. J Exp Med. 2022. PMID: 36069923 Free PMC article.
-
Atherosclerosis: pathogenesis and increased occurrence in individuals with HIV and Mycobacterium tuberculosis infection.HIV AIDS (Auckl). 2010;2:211-8. doi: 10.2147/HIV.S11977. Epub 2010 Oct 29. HIV AIDS (Auckl). 2010. PMID: 22096400 Free PMC article.
-
How to Increase Cellular Glutathione.Antioxidants (Basel). 2023 May 13;12(5):1094. doi: 10.3390/antiox12051094. Antioxidants (Basel). 2023. PMID: 37237960 Free PMC article. Review.
-
Thiols decrease cytokine levels and down-regulate the expression of CD30 on human allergen-specific T helper (Th) 0 and Th2 cells.Clin Exp Immunol. 2001 Mar;123(3):350-60. doi: 10.1046/j.1365-2249.2001.01453.x. Clin Exp Immunol. 2001. PMID: 11298119 Free PMC article.
-
Adjunct N-Acetylcysteine Treatment in Hospitalized Patients With HIV-Associated Tuberculosis Dampens the Oxidative Stress in Peripheral Blood: Results From the RIPENACTB Study Trial.Front Immunol. 2021 Feb 4;11:602589. doi: 10.3389/fimmu.2020.602589. eCollection 2020. Front Immunol. 2021. PMID: 33613521 Free PMC article. Clinical Trial.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials