Effects of S-adenosylmethionine on intrabiliary glutathione degradation induced by long-term administration of cyclosporin A in the rat

• Published in: Toxicology (Amsterdam) 2004-07, Vol.200 (1), p.21-27
• Main Authors: Palomero, Jesús, Galán, Ana I, Muñoz, M.E, González-Gallego, J, Tuñón, Marı́a J, Jiménez, Rafael
• Format: Article
• Language: English
• Subjects: Animals; Bile; Bile - drug effects; Bile - metabolism; Biological and medical sciences; Cyclosporin; Cyclosporine - antagonists & inhibitors; Cyclosporine - pharmacology; Glutathione; Glutathione - secretion; Immunosuppressive Agents - antagonists & inhibitors; Immunosuppressive Agents - pharmacology; Liver - drug effects; Liver - metabolism; Male; Medical sciences; Rats; Rats, Wistar; S-adenosylmethionine; S-Adenosylmethionine - pharmacology; Thiobarbituric Acid Reactive Substances - metabolism; Toxicology
• ISSN: 0300-483X; 1879-3185
• DOI: 10.1016/j.tox.2004.02.030

We investigate the ability of S-adenosylmethionine (SAMe) to antagonize the cyclosporine A (CyA)-induced inhibition of biliary glutathione efflux induced by long-term administration of CyA (10 mg/kg per day-CyA 10 or 20 mg/kg per day-CyA 20 for 4 weeks) in rats. CyA treatment reduced the liver content of total glutathione and caused a significant increase in the oxidized-to-reduced glutathione ratio and the thiobarbituric acid-reactive substances (TBARS) concentration. When the rats were concurrently treated with SAMe (10 mg/kg twice daily) and CyA, all these parameters did not significantly differ from control values. Treatment with CyA induced a significant increase in liver GGT activity that was attenuated by coadministration of SAMe. Biliary efflux of total glutathione was significantly reduced in animals treated with CyA. These changes were abolished by SAMe administration. Following inhibition of the intrabiliary catabolism of the tripeptide by acivicin, glutathione efflux rates increased to a lesser extent in animals cotreated with SAMe when compared to those receiving only CyA. The significant decrease in biliary efflux of oxidized glutathione induced by CyA was totally ( S+CyA 10) or partially ( S+CyA 20) prevented by coadministration of SAMe. Our observations confirm that SAMe cotreatment in rats antagonizes CyA-induced inhibition in the biliary efflux of glutathione and suggest that protection against intrabiliary glutathione degradation plays a major role in this protective effect.