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(2E)-3-[5-(2,3-二甲氧基-6-甲基-1,4-苯醌基)]-2-壬基-2-丙烯酸对小鼠内毒素介导性肝炎的保护作用

Protective effects of (2E)-3-[5-(2,3-dimethoxy-6-methyl-1,4- benzoquinoyl)]-2-nonyl-2-propenoic acid on endotoxin-mediated hepatitis in mice.

作者信息

Nagakawa J, Hishinuma I, Miyamoto K, Hirota K, Abe S, Yamanaka T, Katayama K, Yamatsu I

机构信息

Tsukuba Research Laboratories, Eisai Co., Ltd., Ibaraki, Japan.

出版信息

J Pharmacol Exp Ther. 1992 Jul;262(1):145-50.

PMID:1625194
Abstract

E3330 [(2E)-3-[5-(2,3-dimethoxy-6-methyl-1,4-benzoquinoyl)]-2-nonyl-2- propenoic acid] is a newly synthesized hepatoprotective quinone derivative. We examined the protective effects and possible mechanism of action of E3330 in three different endotoxin (lipopolysaccharide)-induced murine hepatitis models, in which tumor necrosis factor is suggested to play a critical role in the pathogenesis. One of these models was induced by i.v. injection of lipopolysaccharide in combination with D-galactosamine to mice. Oral pretreatment with E3330 improved the survival rate and attenuated the increase in plasma aminotransferase activities of the survivors. The other two models were induced by i.v. injection of lipopolysaccharide or a mixture of D-galactosamine and lipopolysaccharide in Propionibacterium acnes-primed mice. In both of these models, tumor necrosis factor was detected in the plasma within 3 hr of the injection. Oral pretreatment with E3330 attenuated the elevation of plasma tumor necrosis factor activity and protected mice from liver injury. Furthermore, E3330 inhibited the production of tumor necrosis factor from cultured Propionibacterium acnes-elicited murine peritoneal macrophages on stimulation with lipopolysaccharide in vitro. These findings suggest that the inhibition by E3330 of tumor necrosis factor production is the major mechanism of the protective effect of E3330 in these endotoxin-mediated hepatitis models in mice.

摘要

E3330 [(2E)-3-[5-(2,3-二甲氧基-6-甲基-1,4-苯醌基)]-2-壬基-2-丙烯酸]是一种新合成的具有肝脏保护作用的醌衍生物。我们在三种不同的内毒素(脂多糖)诱导的小鼠肝炎模型中研究了E3330的保护作用及其可能的作用机制,在这些模型中,肿瘤坏死因子被认为在发病机制中起关键作用。其中一种模型是通过向小鼠静脉注射脂多糖与D-半乳糖胺联合诱导的。用E3330进行口服预处理可提高存活率,并减轻存活小鼠血浆氨基转移酶活性的升高。另外两种模型是通过向痤疮丙酸杆菌致敏的小鼠静脉注射脂多糖或D-半乳糖胺与脂多糖的混合物诱导的。在这两种模型中,注射后3小时内血浆中均检测到肿瘤坏死因子。用E3330进行口服预处理可减轻血浆肿瘤坏死因子活性的升高,并保护小鼠免受肝损伤。此外,E3330在体外刺激下可抑制脂多糖诱导的痤疮丙酸杆菌激发的小鼠腹腔巨噬细胞产生肿瘤坏死因子。这些发现表明,E3330对肿瘤坏死因子产生的抑制作用是其在这些小鼠内毒素介导的肝炎模型中发挥保护作用的主要机制。

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