Isolated rat hepatocyte couplets were used to study the effect of S-adenosyl-L methionine (SAMe) treatment on disruption of canalicular function caused by cyclosporin A (CyA). Canalicular function was assessed by counting the percentage of couplets that were able to accumulate the fluorescent cholep
S-adenosyl-L-methionine prevents and reverses erythrocyte membrane alterations in cirrhosis
โ Scribed by Pablo Muriel
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 370 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0260-437X
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โฆ Synopsis
Transmethylation is an important means of altering the biological activity of a wide variety of compounds. In human and experimental CC1,-liver cirrhosis the intrahepatic content of Sadenosyl-L-methionine (SAM), an active methyl donor, and the SAM-transmethylase activity are markedly reduced. Previously, it has been reported that SAM administration preserves hepatocyte plasma membrane Na +/K+-ATPase and Ca2+ -ATPase activities in cirrhotic rats. Therefore, the aim of this work was to study the effect of SAM administration on the membrane lipid composition and the ATPase activity on erythrocytes derived from CC1,-cirrhotic rats. Male Wistar rats were used in these experiments. In group 1, cirrhosis was induced by i.p. administration of CC14. Animals of group 2 received, in addition to CCI4, three daily doses of SAM (20 mg kg-', i.m.). Group 3 consisted of cirrhotic animals that, after 8 weeks of CCl, treatment, received SAM (20 mg kg-', i m . , three times daily) for 4 weeks without discontinuation of CCI,. Group 4 included animals treated with SAM alone. Seventy-two hours after the end of treatment the rats were anaesthetized, blood was collected by heart puncture and the erythrocyte plasma membranes were isolated. The Na +/K+-and (Caz + + MgZ+)-ATPase activities and the cholesterol (CH) and phospholipid (PL) contents were determined in the plasma membranes. The Na' /K+and Ca2'-ATPase activities were both significantly decreased (twofold) in the CC1,-treated group as compared to controls. Administration of SAM completely prevented this fall in both ATPases. In group 4, the Na'/K' -ATPase activity was partially restored but the Ca*+-ATPase activity was completely restored. CCI, increased the CH/PL ratio; however, this alteration was not observed in the group treated with CCI, + SAM simultaneously and was completely reversed in group 4. Since the increase in the membrane CH/PL ratio decreases the membrane fluidity and thus changes the enzyme activity, two mechanisms by which SAM preserves the ATPase activity in cirrhotic rats could be by preventing the increase in the CH/PL ratio and by methylation of phospholipids.
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