Suppr超能文献

尿毒症患者肝细胞中内质网的肥大与功能减退。一项形态计量学与生物化学研究。

Hypertrophic and hypoactive smooth endoplasmic reticulum in hepatocytes uremic patients. A morphometric and biochemical study.

作者信息

Kawata S, Seki K, Shinji Y, Tarui S, Sugiyama T, Yamano T

出版信息

Gastroenterol Jpn. 1982;17(3):192-200. doi: 10.1007/BF02775995.

Abstract

Morphometric analysis of the hepatic endoplasmic reticulum and assays of drug-metabolizing enzymes in microsomes prepared from needle biopsy specimens were performed with samples from uremic patients on chronic hemodialysis and normal controls. The smooth endoplasmic reticulum (SER) morphometrically increased in the uremic patients, whereas the cytochrome P-450 content and the activity of p-nitroanisole O-demethylase per mg microsomal protein decreased in the uremic patients. This condition of SER corresponds to that of the so-called hypoactive hypertrophic smooth endoplasmic reticulum, which could suggest lower activity of hepatic microsomal drug oxidation in uremic patients. On the other hand, the P-450 content and the activity of p-nitroanisole O-demethylase per g liver were not significantly different between the uremic and the normal subjects. This seems to indicate that the capacity of drug oxidation is retained in whole livers of uremic patients. However, since some patients in this study showed markedly low activity of p-nitroanisole O-demethylase per mg microsomal protein and per g liver, lipophilic drugs metabolized in the liver as well as hydrophilic ones eliminated by the kidney should be carefully administered to uremic patients.

摘要

对慢性血液透析的尿毒症患者和正常对照者的针吸活检标本制备的微粒体进行肝内质网形态计量分析和药物代谢酶测定。尿毒症患者的滑面内质网(SER)在形态计量上增加,而尿毒症患者每毫克微粒体蛋白的细胞色素P - 450含量和对硝基苯甲醚O - 脱甲基酶活性降低。SER的这种情况与所谓的低活性肥大性滑面内质网的情况相对应,这可能表明尿毒症患者肝微粒体药物氧化活性较低。另一方面,尿毒症患者和正常受试者每克肝脏的P - 450含量和对硝基苯甲醚O - 脱甲基酶活性没有显著差异。这似乎表明尿毒症患者全肝的药物氧化能力得以保留。然而,由于本研究中的一些患者每毫克微粒体蛋白和每克肝脏的对硝基苯甲醚O - 脱甲基酶活性明显较低,对于尿毒症患者,在肝脏中代谢的亲脂性药物以及通过肾脏排泄的亲水性药物都应谨慎给药。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验