• 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

一些选择性毒蕈碱受体拮抗剂对介导兔和大鼠胸主动脉内皮依赖性舒张的毒蕈碱受体的亲和力。

The affinity of some selective muscarinic receptor antagonists for the muscarinic receptor mediating endothelial-dependent relaxation of the rabbit and rat thoracic aorta.

作者信息

Choo L K, Malta E, Mitchelson F

出版信息

J Pharm Pharmacol. 1986 Nov;38(11):843-5. doi: 10.1111/j.2042-7158.1986.tb04507.x.

DOI:10.1111/j.2042-7158.1986.tb04507.x
PMID:2879017
Abstract

The pKB values determined for pirenzepine, 4-DAMP, secoverine and gallamine against acetylcholine-mediated relaxant effects in rabbit aorta indicate that this muscarinic receptor closely resembles that which mediates contraction of non-vascular smooth muscle. The results of the present study argue against the presence of a novel type of muscarinic receptor mediating endothelium-dependent relaxation.

摘要

在兔主动脉中,针对哌仑西平、4-二甲基氨基吡啶(4-DAMP)、西维美林和加拉明对乙酰胆碱介导的舒张作用所测定的pKB值表明,这种毒蕈碱受体与介导非血管平滑肌收缩的受体极为相似。本研究结果反对存在一种介导内皮依赖性舒张的新型毒蕈碱受体。

相似文献

1
The affinity of some selective muscarinic receptor antagonists for the muscarinic receptor mediating endothelial-dependent relaxation of the rabbit and rat thoracic aorta.一些选择性毒蕈碱受体拮抗剂对介导兔和大鼠胸主动脉内皮依赖性舒张的毒蕈碱受体的亲和力。
J Pharm Pharmacol. 1986 Nov;38(11):843-5. doi: 10.1111/j.2042-7158.1986.tb04507.x.
2
Mediation by M3-muscarinic receptors of both endothelium-dependent contraction and relaxation to acetylcholine in the aorta of the spontaneously hypertensive rat.M3毒蕈碱受体介导自发性高血压大鼠主动脉对乙酰胆碱的内皮依赖性收缩和舒张反应。
Br J Pharmacol. 1994 Jun;112(2):519-24. doi: 10.1111/j.1476-5381.1994.tb13104.x.
3
Characterization of muscarinic cholinergic receptors on the endothelium and the smooth muscle of the rabbit thoracic aorta.兔胸主动脉内皮和平滑肌上毒蕈碱型胆碱能受体的特性研究
J Cardiovasc Pharmacol. 1989 Jun;13(6):870-8. doi: 10.1097/00005344-198906000-00009.
4
Inhibition of endothelium-dependent vasorelaxation by arginine analogues: a pharmacological analysis of agonist and tissue dependence.精氨酸类似物对内皮依赖性血管舒张的抑制作用:激动剂和组织依赖性的药理学分析
Br J Pharmacol. 1992 Mar;105(3):643-52. doi: 10.1111/j.1476-5381.1992.tb09033.x.
5
Pharmacological characterization of the vascular muscarinic receptors mediating relaxation and contraction in rabbit aorta.介导兔主动脉舒张和收缩的血管毒蕈碱受体的药理学特性
J Pharmacol Exp Ther. 1991 Sep;258(3):842-50.
6
Inhibitory effect of fentanyl on acetylcholine-induced relaxation in rat aorta.芬太尼对大鼠主动脉中乙酰胆碱诱导舒张的抑制作用。
Anesthesiology. 2004 Jul;101(1):89-96. doi: 10.1097/00000542-200407000-00015.
7
Pharmacological characterization of muscarinic receptors mediating acetylcholine-induced contraction and relaxation in rabbit intrapulmonary arteries.介导乙酰胆碱诱导兔肺内动脉收缩和舒张的毒蕈碱受体的药理学特性
J Pharmacol Exp Ther. 1994 Jul;270(1):269-76.
8
Pharmacological characteristics of the endothelial target for acetylcholine induced vascular relaxation.乙酰胆碱诱导血管舒张的内皮靶点的药理学特性
Life Sci. 2002 Feb 1;70(11):1285-98. doi: 10.1016/s0024-3205(01)01506-5.
9
Endothelial nucleotide-mediated aorta relaxation in aged Watanabe heritable hyperlipidemic rabbits.
J Cardiovasc Pharmacol. 1995 Jul;26(1):119-26. doi: 10.1097/00005344-199507000-00019.
10
Characterization of muscarinic receptors mediating endothelium-dependent relaxation of bovine coronary artery.介导牛冠状动脉内皮依赖性舒张的毒蕈碱受体的特性研究
Eur J Pharmacol. 1991 Jul 23;200(1):25-33. doi: 10.1016/0014-2999(91)90661-9.

引用本文的文献

1
Release of endothelium-derived hyperpolarizing factor (EDHF) by M3 receptor stimulation in guinea-pig coronary artery.豚鼠冠状动脉中M3受体刺激引发内皮源性超极化因子(EDHF)的释放。
Br J Pharmacol. 1995 Jul;115(5):717-22. doi: 10.1111/j.1476-5381.1995.tb14992.x.
2
The interaction of methoctramine and himbacine at atrial, smooth muscle and endothelial muscarinic receptors in vitro.甲氧卡明与辛巴辛在体外对心房、平滑肌和内皮毒蕈碱受体的相互作用。
Br J Pharmacol. 1988 Dec;95(4):1031-8. doi: 10.1111/j.1476-5381.1988.tb11736.x.
3
Methoctramine selectively blocks cardiac muscarinic M2 receptors in vivo.
Naunyn Schmiedebergs Arch Pharmacol. 1988 Sep;338(3):246-9. doi: 10.1007/BF00173395.
4
The interaction of parafluorohexahydrosiladiphenidol at muscarinic receptors in vitro.对氟六氢硅二苯胺醇在体外与毒蕈碱受体的相互作用。
Br J Pharmacol. 1990 Apr;99(4):637-42. doi: 10.1111/j.1476-5381.1990.tb12983.x.
5
Radioligand binding to muscarinic receptors of bovine aortic endothelial cells.放射性配体与牛主动脉内皮细胞毒蕈碱受体的结合
Br J Pharmacol. 1991 Feb;102(2):373-80. doi: 10.1111/j.1476-5381.1991.tb12181.x.
6
Inhibition of endothelium-dependent vasorelaxation by arginine analogues: a pharmacological analysis of agonist and tissue dependence.精氨酸类似物对内皮依赖性血管舒张的抑制作用:激动剂和组织依赖性的药理学分析
Br J Pharmacol. 1992 Mar;105(3):643-52. doi: 10.1111/j.1476-5381.1992.tb09033.x.