Suppr超能文献

氟烷和恩氟烷对离体大鼠肝细胞药物代谢及蛋白质合成的急性影响。

Acute effects of halothane and enflurane on drug metabolism and protein synthesis in isolated rat hepatocytes.

作者信息

Aune H, Bessesen A, Olsen H, Mørland J

出版信息

Acta Pharmacol Toxicol (Copenh). 1983 Nov;53(5):363-8. doi: 10.1111/j.1600-0773.1983.tb03436.x.

Abstract

The metabolism of sulphanilamide, antipyrine and paracetamol was studied in the absence and presence of the anaesthetics halothane and enflurane at three different concentrations (0.5, 1.0 and 2.0 mM) in isolated hepatocytes from the rat. Cell viability and protein synthesis were monitored to evaluate toxic effects. A strong concentration related inhibition of antipyrine oxidation (40-70%) and paracetamol conjugation (20-40%) was caused by both halothane and enflurane. Acetylation of sulphanilamide was not inhibited, however, as a slight augmentation was noticed. A significant dose related decrease of cell viability (3-13%) was caused by both anaesthetics. Dose dependent inhibition of the synthesis of stationary cell proteins (15-60%) and the synthesis/secretion of medium proteins (35-85%) was caused by halothane. Similar but slightly less pronounced effects were caused by enflurane. The present findings show that volatile anaesthetics may have general effects as well as different degrees of specific effects on both membrane bound enzyme and soluble enzyme activities.

摘要

在来自大鼠的离体肝细胞中,研究了在不存在和存在三种不同浓度(0.5、1.0和2.0 mM)的麻醉剂氟烷和恩氟烷的情况下,磺胺、安替比林和对乙酰氨基酚的代谢。监测细胞活力和蛋白质合成以评估毒性作用。氟烷和恩氟烷均导致与浓度相关的安替比林氧化(40 - 70%)和对乙酰氨基酚结合(20 - 40%)的强烈抑制。然而,磺胺的乙酰化未受抑制,反而有轻微增强。两种麻醉剂均导致细胞活力显著的剂量相关性降低(3 - 13%)。氟烷导致静止细胞蛋白质合成(15 - 60%)以及培养基蛋白质合成/分泌(35 - 85%)的剂量依赖性抑制。恩氟烷也有类似但稍弱的作用。目前的研究结果表明,挥发性麻醉剂可能对膜结合酶和可溶性酶活性既有一般影响,也有不同程度的特定影响。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验