• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

[钙拮抗剂、钾通道开放剂治疗充血性心力衰竭患者]

[Ca-antagonist, K-channel-opener in the treatment of patients with congestive heart failure].

作者信息

Satoh K

机构信息

Department of Pharmacology, Faculty of Medicine, Tottori University.

出版信息

Nihon Rinsho. 1993 May;51(5):1293-8.

PMID:8331797
Abstract

The development of vasodilator drugs that open the K+ channels in blood vessels has been of great academic and practical interest. The K-channel openers (cromakalim, pinacidil and nicorandil) decreased afterload or preload due to their vasodilator action. In addition, K-channel openers produced a cardioprotective effect in lower doses that did not affect coronary blood flow or blood pressure. It is highly expected to be useful for treatment of congestive heart failure.

摘要

开发能打开血管中钾通道的血管扩张药物具有重大的学术和实际意义。钾通道开放剂(色满卡林、匹那地尔和尼可地尔)因其血管扩张作用而降低后负荷或前负荷。此外,钾通道开放剂在不影响冠状动脉血流或血压的较低剂量下产生心脏保护作用。人们高度期望它对治疗充血性心力衰竭有用。

相似文献

1
[Ca-antagonist, K-channel-opener in the treatment of patients with congestive heart failure].[钙拮抗剂、钾通道开放剂治疗充血性心力衰竭患者]
Nihon Rinsho. 1993 May;51(5):1293-8.
2
[The vasospasmolytic effects of nicorandil, cromakalim and pinacidil on 3,4-diaminopyridine-induced phasic contractions in canine coronary arteries as an experimental vasospasm model].[以犬冠状动脉3,4-二氨基吡啶诱导的相性收缩作为实验性血管痉挛模型,探讨尼可地尔、克罗卡林和平卡地尔对其血管痉挛的缓解作用]
Nihon Yakurigaku Zasshi. 1992 Oct;100(4):317-27. doi: 10.1254/fpj.100.317.
3
Cytoplasmic calcium and the relaxation of canine coronary arterial smooth muscle produced by cromakalim, pinacidil and nicorandil.细胞质钙与克罗卡林、匹那地尔和尼可地尔引起的犬冠状动脉平滑肌舒张
Br J Pharmacol. 1990 Sep;101(1):157-65. doi: 10.1111/j.1476-5381.1990.tb12106.x.
4
Cromakalim, a potassium channel activator: a comparison of its cardiovascular haemodynamic profile and tissue specificity with those of pinacidil and nicorandil.克罗卡林,一种钾通道激活剂:其心血管血流动力学特征及组织特异性与匹那地尔和尼可地尔的比较
J Cardiovasc Pharmacol. 1988;12(5):535-42.
5
Potassium channel activator drugs: mechanism of action, pharmacological properties, and therapeutic potential.钾通道激活剂药物:作用机制、药理特性及治疗潜力。
Med Res Rev. 1992 Mar;12(2):73-148. doi: 10.1002/med.2610120202.
6
Effect of three novel K+ channel openers, cromakalim, pinacidil and nicorandil on allergic reaction and experimental asthma.三种新型钾通道开放剂(克罗卡林、匹那地尔和尼可地尔)对过敏反应和实验性哮喘的影响。
Jpn J Pharmacol. 1991 May;56(1):13-21. doi: 10.1254/jjp.56.13.
7
Effects of ATP-sensitive K+ channel openers on pacemaker activity in isolated single rabbit sino-atrial node cells.ATP敏感性钾通道开放剂对离体单个兔窦房结细胞起搏活动的影响。
J Cardiovasc Pharmacol. 1993 Dec;22(6):863-8. doi: 10.1097/00005344-199312000-00014.
8
Pharmacology and structure-activity relationships for KATP modulators: tissue-selective KATP openers.KATP调节剂的药理学及构效关系:组织选择性KATP开放剂
J Cardiovasc Pharmacol. 1994;24 Suppl 4:S12-7.
9
Potassium channel modulation: a new drug principle for regulation of smooth muscle contractility. Studies on isolated airways and arteries.钾通道调节:一种调节平滑肌收缩性的新药理原则。对离体气道和动脉的研究。
Dan Med Bull. 1996 Dec;43(5):429-47.
10
Effects of K-channel openers on the contractility and electrical activity of antral circular muscle in guinea-pig stomach.
J Smooth Muscle Res. 1993 Oct;29(5):145.