• 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

N-阿魏酰酪胺(酪胺类似物)对蛙心室肌细胞内向整流钾通道的作用。

Effect of N-feruloyl tyramine (an analogue of tyramine) on inwardly rectifying potassium channel in frog ventricular myocytes.

作者信息

Munemori M, Yamaoka K, Yusuf I, Sumii K, Otsuka H, Yamasaki K

机构信息

Department of Physiology, Hiroshima University School of Medicine, Japan.

出版信息

Hiroshima J Med Sci. 1996 Mar;45(1):31-5.

PMID:8984103
Abstract

Electrophysiological effects of N-feruloyl tyramine (NFT), an analogue of tyramine, on potassium currents in frog ventricular myocytes were examined using single-channel recording and whole-cell voltage clamp technique. Extracellular application of NFT induced a concentration-dependent decrease of macroscopic inward rectifier potassium current (iK1) with ID50 of 198 microM, while tyramine (100 microM) was ineffective in producing an inhibitory effect on iK1. NFT reduced the mean open time of iK1 to 1.3 ms from 3.1 ms in control without affecting the amplitude of single-channel conductance. It is indicated that boi containing NFT produces a prolongation of the plateau phase caused by the suppression of inwardly rectifying K channel. Thus, this prolongation may induce an increase in the inflow of Ca ions, which in turn leads to a positive inotropic effect.

摘要

使用单通道记录和全细胞膜片钳技术,研究了酪胺类似物N-阿魏酰酪胺(NFT)对蛙心室肌细胞钾电流的电生理效应。细胞外施加NFT可引起宏观内向整流钾电流(iK1)浓度依赖性降低,半数抑制浓度(ID50)为198微摩尔,而酪胺(100微摩尔)对iK1无抑制作用。NFT将iK1的平均开放时间从对照时的3.1毫秒缩短至1.3毫秒,而不影响单通道电导幅度。结果表明,含NFT的生物制剂通过抑制内向整流钾通道,使平台期延长。因此,这种延长可能导致钙离子内流增加,进而产生正性肌力作用。

相似文献

1
Effect of N-feruloyl tyramine (an analogue of tyramine) on inwardly rectifying potassium channel in frog ventricular myocytes.N-阿魏酰酪胺(酪胺类似物)对蛙心室肌细胞内向整流钾通道的作用。
Hiroshima J Med Sci. 1996 Mar;45(1):31-5.
2
A new class III antiarrhythmic drug, MS-551, blocks the inward rectifier potassium channel in isolated guinea pig ventricular myocytes.一种新型III类抗心律失常药物MS - 551可阻断豚鼠离体心室肌细胞的内向整流钾通道。
J Pharmacol Exp Ther. 1995 Jul;274(1):469-74.
3
Block of sodium channels by tyramine and its analogue (N-feruloyl tyramine) in frog ventricular myocytes.酪胺及其类似物(N-阿魏酰酪胺)对蛙心室肌细胞钠通道的阻断作用。
Jpn J Physiol. 1992;42(2):179-91. doi: 10.2170/jjphysiol.42.179.
4
Effects of nitric oxide donors, S-nitroso-L-cysteine and sodium nitroprusside, on the whole-cell and single channel currents in single myocytes of the guinea-pig proximal colon.一氧化氮供体S-亚硝基-L-半胱氨酸和硝普钠对豚鼠近端结肠单个肌细胞全细胞电流和单通道电流的影响。
Br J Pharmacol. 1998 Feb;123(3):505-17. doi: 10.1038/sj.bjp.0701605.
5
The effects of propofol on macroscopic and single channel sodium currents in rat ventricular myocytes.丙泊酚对大鼠心室肌细胞宏观和单通道钠电流的影响。
Br J Pharmacol. 1998 Jun;124(4):655-62. doi: 10.1038/sj.bjp.0701876.
6
Acute effects of thyroid hormone on inward rectifier potassium channel currents in guinea pig ventricular myocytes.
Endocrinology. 1996 Nov;137(11):4744-51. doi: 10.1210/endo.137.11.8895342.
7
Unitary current through the inward rectifier K+ channel cloned from rabbit heart--comparison with the native K+ channel.通过从兔心脏克隆的内向整流钾通道的单一电流——与天然钾通道的比较
J Mol Cell Cardiol. 1996 May;28(5):957-65. doi: 10.1006/jmcc.1996.0089.
8
Cortistatin increase of a potassium conductance in rat locus coeruleus in vitro.体外培养条件下,大鼠蓝斑中促皮质素抑制素对钾离子电导的增强作用。
Br J Pharmacol. 1997 Dec;122(8):1567-72. doi: 10.1038/sj.bjp.0701541.
9
Electrical remodeling of membrane ionic channels of hypertrophied ventricular myocytes from spontaneously hypertensive rats.自发性高血压大鼠肥厚心室肌细胞膜离子通道的电重构
Chin Med J (Engl). 2000 Jul;113(7):584-7.
10
Alternation of inwardly rectifying background K+ channel during development of rat fetal cardiomyocytes.大鼠胎儿心肌细胞发育过程中内向整流背景钾离子通道的变化
J Mol Cell Cardiol. 2001 Mar;33(3):533-43. doi: 10.1006/jmcc.2000.1327.