Ogawa M, Mori Y, Mor T, Ueda S, Azemoto R, Makino Y, Wakashin Y, Wakashin M, Ohto M, Yoshida H
First Department of Internal Medicine, Chiba University School of Medicine.
Arerugi. 1990 Apr;39(4):418-23.
Acute hepatic necrosis was induced by a single i.v. injection of lipopolysaccharide (LPS) into C57BL/6 mice following immunization with syngeneic liver protein and adjuvant. Sixty percent of the mice died of massive hepatocyte necrosis within 48 hours of LPS injection. The serum lactate dehydrogenase and aspartate aminotransferase levels were markedly elevated. The fatal and hepatotoxic action of LPS was prevented by pretreatment with FUT-175 (1.6 mg/kg), a synthetic protease-inhibitor. The inhibitory effects of FUT-175 was not demonstrated when the agent was given to the mice 2 h after the administration of LPS. These results seem to indicate that the hepatotoxic effects of LPS are mediated by endogenous host mechanisms in which proteases play an important role.
在用同基因肝蛋白和佐剂免疫C57BL/6小鼠后,通过静脉内单次注射脂多糖(LPS)诱导急性肝坏死。60%的小鼠在LPS注射后48小时内死于大量肝细胞坏死。血清乳酸脱氢酶和天冬氨酸转氨酶水平显著升高。合成蛋白酶抑制剂FUT-175(1.6mg/kg)预处理可预防LPS的致死和肝毒性作用。当在给予LPS后2小时给小鼠施用该药物时,未显示FUT-175的抑制作用。这些结果似乎表明,LPS的肝毒性作用是由内源性宿主机制介导的,其中蛋白酶起重要作用。