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在喂食胆固醇的日本鹌鹑中比较胆汁酸螯合剂消胆胺和盐酸考来替泊的降胆固醇活性。

Comparison of hypocholesterolemic activities of the bile acid sequestrants cholestyramine and colestipol hydrochloride in cholesterol fed SEA quail.

作者信息

Day C E

机构信息

Audax, Inc. Leitchfield, KY 42754.

出版信息

Artery. 1990;17(5):281-8.

PMID:2396902
Abstract

The pharmacopolymer bile acid sequestrants cholestyramine and colestipol hydrochloride were mixed with a diet supplemented with 0.5% cholesterol at levels of 0.25%, 0.5%, and 1.0% for cholestyramine and 0.5% and 1.0% for colestipol and fed to young, male, SEA (Susceptible to Experimental Atherosclerosis) Japanese quail (Coturnix coturnix japonica) for a period of seven days. After treatment blood was obtained by venipuncture from non-fasted animals and analyzed for serum total cholesterol concentration. Cholestyramine significantly reduced total cholesterol concentrations at all doses in a dose dependent manner. Colestipol significantly reduced total cholesterol only at the 1.0% dose. Based on these observations, cholestyramine is significantly more potent for reducing serum cholesterol in hypercholesterolemic male SEA quail than is colestipol hydrochloride.

摘要

将高分子聚合物胆汁酸螯合剂考来烯胺和盐酸考来替泊,分别按0.25%、0.5%和1.0%的水平(考来烯胺)以及0.5%和1.0%的水平(盐酸考来替泊),与添加了0.5%胆固醇的饲料混合,喂给年轻的雄性SEA(易患实验性动脉粥样硬化)日本鹌鹑(日本鹌鹑),为期7天。处理后,通过静脉穿刺从非禁食动物获取血液,并分析血清总胆固醇浓度。考来烯胺在所有剂量下均以剂量依赖性方式显著降低总胆固醇浓度。盐酸考来替泊仅在1.0%剂量时显著降低总胆固醇。基于这些观察结果,考来烯胺在降低高胆固醇血症雄性SEA鹌鹑血清胆固醇方面比盐酸考来替泊显著更有效。

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