Suppr超能文献

16,16-二甲基前列腺素E2可延缓大鼠肝脏营养性损伤中胶原蛋白的形成。

16,16-Dimethyl prostaglandin E2 delays collagen formation in nutritional injury in rat liver.

作者信息

Ruwart M J, Rush B D, Snyder K F, Peters K M, Appelman H D, Henley K S

机构信息

Diabetes and Gastrointestinal Diseases Research, Upjohn Company, Kalamazoo, Michigan 49001.

出版信息

Hepatology. 1988 Jan-Feb;8(1):61-4. doi: 10.1002/hep.1840080112.

Abstract

Chronic nutritional injury was induced in rats by a high-fat, lipotrope-deficient diet. The hepatoprotective effect of 16,16-dimethyl prostaglandin E2 on the deposition of collagen and fat was assessed by histological evaluation and measurement of hydroxyproline. Dose-response studies established that optimal protection was achieved by the twice daily administration of 16,16-dimethyl prostaglandin E2 at 100 micrograms per kg (subcutaneous) or 250 micrograms per kg (oral). 16,16-Dimethyl prostaglandin E2 and a crystalline analog [(p-acetamidobenzamido)phenyl ester of 16,16-dimethyl prostaglandin E2 significantly delayed both the deposition of collagen and the increase in hepatic hydroxyproline content. There was an excellent correlation between the histological assessment of collagen and the biochemical measurement of hydroxyproline. These data provide a rationale for the evaluation of prostaglandins in the treatment of human liver disease.

摘要

通过高脂、缺乏促脂物质的饮食诱导大鼠发生慢性营养损伤。通过组织学评估和羟脯氨酸测量来评估16,16-二甲基前列腺素E2对胶原蛋白和脂肪沉积的肝保护作用。剂量反应研究表明,每天两次皮下注射16,16-二甲基前列腺素E2,剂量为每千克100微克,或口服每千克250微克,可实现最佳保护。16,16-二甲基前列腺素E2及其晶体类似物[16,16-二甲基前列腺素E2的(对乙酰氨基苯甲酰胺基)苯酯]显著延缓了胶原蛋白的沉积和肝脏羟脯氨酸含量的增加。胶原蛋白的组织学评估与羟脯氨酸的生化测量之间存在良好的相关性。这些数据为评估前列腺素在治疗人类肝脏疾病中的作用提供了理论依据。

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