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丙咪嗪对四氯化碳诱导的中毒后期肝坏死的预防作用。

Imipramine prevention of carbon tetrachloride-induced liver necrosis at late states of the intoxication process.

作者信息

Fernández G, Villarruel M C, de Ferreyra E C, de Fenos O M, Castro J A

出版信息

J Appl Toxicol. 1986 Dec;6(6):413-8. doi: 10.1002/jat.2550060606.

Abstract

Imipramine administration (50 mg kg-1, i.p.) to Sprague-Dawley male rats (240-290 g) 6 or 10 h after CCl4 (1 ml kg-1, i.p.) partially prevents liver necrosis induced by the hepatotoxin. When imipramine is given 30 min before CCl4, it inhibits in part the CCl4-induced lipid peroxidation and the covalent interactions of reactive metabolites with microsomal lipids or proteins and partially prevents CCl4-induced cytochrome P-450 destruction, but not glucose 6 phosphatase activity depression. Imipramine administration prior to CCl4 does not modify levels of the hepatotoxin reaching the liver or the body temperature of CCl4 treated animals. Early preventive effects of imipramine on cytochrome P-450, might be attributed to inhibition of covalent interactions of reactive metabolites. The hypothesis that imipramine exerted late preventive effects by interfering with calcium deleterious effects or by modulation of protein and phospholipid synthesis or degradation is analyzed.

摘要

在给雄性Sprague-Dawley大鼠(240 - 290克)腹腔注射四氯化碳(1毫升/千克)6或10小时后,腹腔注射丙咪嗪(50毫克/千克)可部分预防由该肝毒素诱导的肝坏死。当在注射四氯化碳前30分钟给予丙咪嗪时,它可部分抑制四氯化碳诱导的脂质过氧化以及反应性代谢产物与微粒体脂质或蛋白质的共价相互作用,并部分预防四氯化碳诱导的细胞色素P - 450破坏,但不能预防葡萄糖6磷酸酶活性降低。在四氯化碳注射前给予丙咪嗪不会改变到达肝脏的肝毒素水平或四氯化碳处理动物的体温。丙咪嗪对细胞色素P - 450的早期预防作用可能归因于对反应性代谢产物共价相互作用的抑制。分析了丙咪嗪通过干扰钙的有害作用或通过调节蛋白质和磷脂的合成或降解发挥后期预防作用的假说。

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