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The effects of age and hyperhomocysteinemia on the redox forms of plasma thiols.
J Lab Clin Med 2004; 144(5):235-45JL

Abstract

We assayed the redox forms of cysteine (reduced [CSH], oxidized [CSSC], and bound to protein [CS-SP]), cysteinylglycine (CGSH; cysteinylgycine disulfide [CGSSGC] and cysteinylglycine-protein mixed disulfide [CGS-SP]), glutathione (GSH; glutathione disulfide [GSSG] and glutathione-protein mixed disulfide [GS-SP]), homocysteine (Hcy; homocystine [HcyS] and homocystine-protein mixed disulfides [bHcy]), and protein sulfhydryls in the plasma of healthy subjects (divided into 8 groups ranging in age from birth to 70 years) and patients with mild hyperhomocysteinemia associated with cardiovascular disease (heart-transplant patients) or vascular atherosclerosis, with or without renal failure. In healthy individuals, levels of disulfides and protein-mixed disulfides were more abundant than those of thiols, and those of protein-thiol mixed disulfides were higher than disulfides. Concentrations of CSH, GSH, and CGSH in the various groups had profiles characterized by a maximum over time. The concentration of Hcy was unchanged up to the age of 30 years, after which it increased. CSSC concentration increased gradually with age, whereas concentrations of the other disulfides were essentially unchanged. By contrast, the concentrations of all protein-thiol mixed disulfides, especially those with CSH, increased gradually with age. Ranks of distribution of the reduced forms changed with age (at birth, CSH > CGSH > GSH > Hcy; in 1- to 2-year-olds, CSH > GSH > CGSH > Hcy; and in 51- to 70-year-olds, CSH > CGSH = GSH > Hcy), whereas those of disulfides and protein-thiol mixed disulfides were substantially unchanged (in all age groups, CSSC > CGSSGC > GSSG = HcyS and CS-SP > CGS-SP > bHcy > GS-SP). In patients with pathologic conditions, plasma levels of disulfide forms CSSC, HcyS, CS-SP, and bHcy were significantly increased, whereas other redox forms of thiols were unchanged or showed variations opposite (increasing or decreasing) to control values. Maximal increases in disulfides and protein-thiol mixed disulfides were associated with renal failure. Our data suggest that increases in plasma bHcy concentrations in subjects with pathologic conditions were more likely the result of activation of thiol-disulfide exchange reactions between free reduced Hcy and CS-SP than of a direct action of reactive oxygen species.

Authors+Show Affiliations

Department of Neuroscience, Pharmacology Unit, University of Sienna, Sienna, Italy.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Comparative Study
Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

15570241

Citation

Di Giuseppe, Danila, et al. "The Effects of Age and Hyperhomocysteinemia On the Redox Forms of Plasma Thiols." The Journal of Laboratory and Clinical Medicine, vol. 144, no. 5, 2004, pp. 235-45.
Di Giuseppe D, Frosali S, Priora R, et al. The effects of age and hyperhomocysteinemia on the redox forms of plasma thiols. J Lab Clin Med. 2004;144(5):235-45.
Di Giuseppe, D., Frosali, S., Priora, R., Di Simplicio, F. C., Buonocore, G., Cellesi, C., ... Di Simplicio, P. (2004). The effects of age and hyperhomocysteinemia on the redox forms of plasma thiols. The Journal of Laboratory and Clinical Medicine, 144(5), pp. 235-45.
Di Giuseppe D, et al. The Effects of Age and Hyperhomocysteinemia On the Redox Forms of Plasma Thiols. J Lab Clin Med. 2004;144(5):235-45. PubMed PMID: 15570241.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - The effects of age and hyperhomocysteinemia on the redox forms of plasma thiols. AU - Di Giuseppe,Danila, AU - Frosali,Simona, AU - Priora,Raffaella, AU - Di Simplicio,Francesca Cherubini, AU - Buonocore,Giuseppe, AU - Cellesi,Carla, AU - Capecchi,Pier Leopoldo, AU - Pasini,Franco Laghi, AU - Lazzerini,Pietro Enea, AU - Jakubowski,Hieronim, AU - Di Simplicio,Paolo, PY - 2004/12/1/pubmed PY - 2004/12/24/medline PY - 2004/12/1/entrez SP - 235 EP - 45 JF - The Journal of laboratory and clinical medicine JO - J. Lab. Clin. Med. VL - 144 IS - 5 N2 - We assayed the redox forms of cysteine (reduced [CSH], oxidized [CSSC], and bound to protein [CS-SP]), cysteinylglycine (CGSH; cysteinylgycine disulfide [CGSSGC] and cysteinylglycine-protein mixed disulfide [CGS-SP]), glutathione (GSH; glutathione disulfide [GSSG] and glutathione-protein mixed disulfide [GS-SP]), homocysteine (Hcy; homocystine [HcyS] and homocystine-protein mixed disulfides [bHcy]), and protein sulfhydryls in the plasma of healthy subjects (divided into 8 groups ranging in age from birth to 70 years) and patients with mild hyperhomocysteinemia associated with cardiovascular disease (heart-transplant patients) or vascular atherosclerosis, with or without renal failure. In healthy individuals, levels of disulfides and protein-mixed disulfides were more abundant than those of thiols, and those of protein-thiol mixed disulfides were higher than disulfides. Concentrations of CSH, GSH, and CGSH in the various groups had profiles characterized by a maximum over time. The concentration of Hcy was unchanged up to the age of 30 years, after which it increased. CSSC concentration increased gradually with age, whereas concentrations of the other disulfides were essentially unchanged. By contrast, the concentrations of all protein-thiol mixed disulfides, especially those with CSH, increased gradually with age. Ranks of distribution of the reduced forms changed with age (at birth, CSH > CGSH > GSH > Hcy; in 1- to 2-year-olds, CSH > GSH > CGSH > Hcy; and in 51- to 70-year-olds, CSH > CGSH = GSH > Hcy), whereas those of disulfides and protein-thiol mixed disulfides were substantially unchanged (in all age groups, CSSC > CGSSGC > GSSG = HcyS and CS-SP > CGS-SP > bHcy > GS-SP). In patients with pathologic conditions, plasma levels of disulfide forms CSSC, HcyS, CS-SP, and bHcy were significantly increased, whereas other redox forms of thiols were unchanged or showed variations opposite (increasing or decreasing) to control values. Maximal increases in disulfides and protein-thiol mixed disulfides were associated with renal failure. Our data suggest that increases in plasma bHcy concentrations in subjects with pathologic conditions were more likely the result of activation of thiol-disulfide exchange reactions between free reduced Hcy and CS-SP than of a direct action of reactive oxygen species. SN - 0022-2143 UR - https://www.unboundmedicine.com/medline/citation/15570241/The_effects_of_age_and_hyperhomocysteinemia_on_the_redox_forms_of_plasma_thiols_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S0022214304002148 DB - PRIME DP - Unbound Medicine ER -