Suppr超能文献

6-氨基-2-巯基-5-甲基嘧啶-4-羧酸对大鼠和组织培养细胞的降血脂作用

Hypolipidemic effects of 6-amino-2-mercapto-5-methylpyrimidine-4-carboxylic acid in rats and tissue culture cells.

作者信息

Hall I H, Wong O T, Reynolds D J, Simlot R, Chang J J

机构信息

Division of Medicinal Chemistry and Natural Products, School of Pharmacy, University of North Carolina, Chapel Hill 27599-7360.

出版信息

J Pharm Sci. 1993 Jan;82(1):60-8. doi: 10.1002/jps.2600820114.

Abstract

6-Amino-2-mercapto-5-methylpyrimidine-4-carboxylic acid (AMMPCA) was found to be a potent hypolipidemic agent at oral doses of 10 and 20 mg/kg/day in rodents. This agent was observed to affect de novo lipid synthesizing enzyme activities in a manner that resulted in lower lipid levels in tissues including the aorta wall. Very low density lipoprotein and low density lipoprotein cholesterol levels were reduced, whereas high density lipoprotein cholesterol levels were significantly increased. AMMPCA interfered with low density receptor activity, suggesting that the drug blocked lipid uptake by peripheral tissue while stimulating binding of lipid to the high density lipoprotein receptor, which should accelerate lipid clearance from the tissues and blood. A second mode of action of the drug is enhanced biliary excretion of lipids, but there was no evidence of a lithogenic effect. Acute toxicity studies in rodents support the fact that AMMPCA is safe in its therapeutic dose range.

摘要

6-氨基-2-巯基-5-甲基嘧啶-4-羧酸(AMMPCA)在啮齿动物中口服剂量为10和20毫克/千克/天时被发现是一种有效的降血脂药物。观察到该药物以一种导致包括主动脉壁在内的组织中脂质水平降低的方式影响从头脂质合成酶活性。极低密度脂蛋白和低密度脂蛋白胆固醇水平降低,而高密度脂蛋白胆固醇水平显著升高。AMMPCA干扰低密度受体活性,表明该药物阻断外周组织对脂质的摄取,同时刺激脂质与高密度脂蛋白受体的结合,这应该会加速脂质从组织和血液中的清除。该药物的第二种作用方式是增强脂质的胆汁排泄,但没有致石作用的证据。啮齿动物的急性毒性研究支持了AMMPCA在其治疗剂量范围内是安全的这一事实。

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