Wang Xiaodong, Cederbaum Arthur I
Department of Pharmacology and Systems Therapeutics, Mount Sinai School of Medicine, One Gustave L. Levy Place, 1468 Madison Avenue, New York, NY 10029, USA.
Arch Biochem Biophys. 2008 Sep 1;477(1):1-11. doi: 10.1016/j.abb.2008.04.033. Epub 2008 Apr 30.
The current study was designed to investigate the effect and potential mechanism of exogenous administration of S-adenosyl-l-methionine (SAM) on the enhanced hepatotoxicity induced by the Fas agonistic Jo2 antibody plus acute ethanol pretreatment in C57BL/6 mice. Acute ethanol plus Jo2 treatment produces liver toxicity under conditions in which ethanol alone or Jo2 alone do not. SAM significantly attenuated this elevated hepatotoxicity in mice as manifested by a decrease of serum aminotransferases and morphological amelioration. Levels of SAM and activity of methionine adenosyltransferase were lowered by the ethanol plus Jo2 treatment but restored by administration of SAM. The ethanol plus Jo2 treatment increased activity and content of CYP2E1, iNOS content and TNF-alpha levels; these increases were blunted by SAM. SAM also protected against the elevated oxidative and nitrosative stress found after ethanol plus Jo2, likely due to the decreases in CYP2E1, iNOS and TNF-alpha. Calcium-induced swelling of mitochondria was enhanced by the ethanol plus Jo2 treatment and this was prevented by SAM. JNK and P38 MAPK were activated by the ethanol plus Jo2 treatment; JNK activation was partially prevented by SAM. It is suggested that SAM protects against the ethanol plus Jo2 toxicity by restoring hepatic SAM levels, preventing the increase in iNOS, CYP2E1 and TNF-alpha and there by lowering the elevated oxidative/nitrosative stress and activation of the JNK signal pathway, ultimately preventing mitochondrial damage.
本研究旨在探讨外源性给予S-腺苷-L-甲硫氨酸(SAM)对Fas激动剂Jo2抗体联合急性乙醇预处理诱导的C57BL/6小鼠肝毒性增强的影响及潜在机制。急性乙醇联合Jo2处理在单独乙醇或单独Jo2处理不产生肝毒性的条件下可导致肝毒性。SAM显著减轻了小鼠这种升高的肝毒性,表现为血清转氨酶降低和形态学改善。乙醇联合Jo2处理降低了SAM水平和甲硫氨酸腺苷转移酶活性,但给予SAM后得以恢复。乙醇联合Jo2处理增加了CYP2E1的活性和含量、iNOS含量以及TNF-α水平;这些增加被SAM减弱。SAM还能保护小鼠免受乙醇联合Jo2处理后升高的氧化应激和亚硝化应激,这可能是由于CYP2E1、iNOS和TNF-α的减少。乙醇联合Jo2处理增强了钙诱导的线粒体肿胀,而SAM可预防这种肿胀。乙醇联合Jo2处理激活了JNK和P38 MAPK;SAM部分阻止了JNK的激活。提示SAM通过恢复肝脏SAM水平、防止iNOS、CYP2E1和TNF-α增加,从而降低升高的氧化/亚硝化应激和JNK信号通路的激活,最终预防线粒体损伤,来保护小鼠免受乙醇联合Jo2的毒性作用。