Suppr超能文献

新型吡啶甲脒类KATP通道开放剂KRN4884对大鼠血清甘油三酯水平的影响。

Effects of KRN4884, a novel pyridinecarboxamidine type KATP channel opener, on serum triglyceride levels in rats.

作者信息

Yokoyama T, Izumi H, Endoh M, Izawa T, Ogawa N, Okada Y

机构信息

Pharmaceutical Research Laboratory, Kirin Brewery, Co., Ltd., Gunma, Japan.

出版信息

Br J Pharmacol. 1997 Apr;120(8):1471-6. doi: 10.1038/sj.bjp.0701077.

Abstract
  1. The effects of KRN4884, a novel pyridinecarboxamidine type KATP channel opener, on serum triglyceride levels were investigated in Sprague-Dawley rats. 2. Oral administration of KRN4884 (3 mg kg-1) for 10 days caused a significant reduction in serum triglyceride levels, which was comparable to that of clofibrate (160 mg kg-1). Reduction in serum triglyceride levels by KRN4884 and clofibrate were accompanied by a reduction in triglyceride levels both in chylomicron and in very low density lipoprotein. KRN4884 treatment did not affect serum concentrations of total cholesterol and phospholipid, but did increase free fatty acid levels. Clofibrate reduced total cholesterol, phospholipid and free fatty acid levels. 3. Administration of clofibrate significantly decreased triglyceride secretion rate as measured by the Triton WR-1339 injection procedure, while KRN4884 did not. 4. Rats receiving KRN4884 exhibited an increase in lipoprotein lipase (LPL) activity both in adipose tissue and in skeletal muscle. There was an inverse correlation between serum triglyceride levels and tissue LPL activities. KRN4884 did not change hepatic triglyceride lipase (HTGL) activity. Clofibrate affected neither LPL nor HTGL activities. 5. It is concluded that administration of KRN4884 results in reduced serum triglyceride levels which may be due to the enhancement of LPL activity in peripheral tissues.
摘要
  1. 在斯普拉格-道利大鼠中研究了新型吡啶甲脒类ATP敏感性钾通道开放剂KRN4884对血清甘油三酯水平的影响。2. 口服KRN4884(3毫克/千克)10天可使血清甘油三酯水平显著降低,这与氯贝丁酯(160毫克/千克)相当。KRN4884和氯贝丁酯降低血清甘油三酯水平的同时,乳糜微粒和极低密度脂蛋白中的甘油三酯水平也降低。KRN4884治疗不影响血清总胆固醇和磷脂浓度,但会增加游离脂肪酸水平。氯贝丁酯降低总胆固醇、磷脂和游离脂肪酸水平。3. 通过注射曲拉通WR-1339测量,氯贝丁酯给药显著降低甘油三酯分泌率,而KRN4884则无此作用。4. 接受KRN4884的大鼠脂肪组织和骨骼肌中的脂蛋白脂肪酶(LPL)活性均增加。血清甘油三酯水平与组织LPL活性呈负相关。KRN4884不改变肝甘油三酯脂肪酶(HTGL)活性。氯贝丁酯对LPL和HTGL活性均无影响。5. 得出结论,给予KRN4884可降低血清甘油三酯水平,这可能是由于外周组织中LPL活性增强所致。

相似文献

6
In vitro and in vivo vasodilating effects of KRN4884, Ki1769 and Ki3005, pyridinecarboxamidine derivatives.
Fundam Clin Pharmacol. 1997;11(6):561-6. doi: 10.1111/j.1472-8206.1997.tb00861.x.

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