• 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

利美尼定对清醒去窦主动脉神经大鼠的交感抑制作用。

Sympathoinhibitory action of rilmenidine in conscious sinoaortically denervated rats.

作者信息

Mayorov D, Chernobelski M, Medvedev O

机构信息

Laboratory of Experimental Pharmacology, National Cardiology Research Center, Moscow, Russia.

出版信息

J Cardiovasc Pharmacol. 1993 Aug;22(2):314-20. doi: 10.1097/00005344-199308000-00022.

DOI:10.1097/00005344-199308000-00022
PMID:7692175
Abstract

The responses of mean arterial pressure (MAP), heart rate (HR), and renal sympathetic nerve activity (RSNA) to rilmenidine administration and changes in these responses after idazoxan or yohimbine pretreatment were investigated in conscious sinoaortically denervated rats. Intravenous (i.v.) injection of rilmenidine (300 and 600 micrograms/kg) dose-dependently reduced MAP (16 and 24%, respectively) and RSNA (31 and 56%, respectively), whereas bradycardia was similar at both doses of the drug. Intracisternal (i.c.) pretreatment with idazoxan (5 micrograms/kg), alpha 2-adrenoceptor antagonist with a high affinity to imidazoline receptors (IR) prevented rilmenidine-induced decreases in MAP but not in RSNA and HR. Rilmenidine (300 micrograms/kg i.c.) significantly decreased MAP by 24%, RSNA by 32%, and HR by 13%. Pretreatment with idazoxan (1 microgram/kg i.c.) significantly attenuated the hypotensive and sympathoinhibitory effects of rilmenidine, whereas i.c. pretreatment with equimolar to 10-fold higher doses of yohimbine, an alpha 2-antagonist that binds poorly with IR, did not. Both idazoxan and yohimbine failed to affect the rilmenidine-induced bradycardia, however. We concluded that (a) rilmenidine exhibits more marked hypotensive effect when injected i.c. than when injected i.v., (b) a part of the inhibitory effect of i.v.-injected rilmenidine on RSNA may be exerted through idazoxan-insensitive mechanisms which might be activated by peripheral action of the drug, and (c) the hypotensive action of rilmenidine relates more to the interaction with IR than with alpha 2-adrenoceptors.

摘要

在清醒的经窦主动脉去神经支配的大鼠中,研究了平均动脉压(MAP)、心率(HR)和肾交感神经活动(RSNA)对瑞米吉仑给药的反应以及在给予咪唑克生或育亨宾预处理后这些反应的变化。静脉注射(i.v.)瑞米吉仑(300和600微克/千克)剂量依赖性地降低MAP(分别为16%和24%)和RSNA(分别为31%和56%),而两种剂量的药物引起的心动过缓相似。对咪唑啉受体(IR)具有高亲和力的α2 -肾上腺素能受体拮抗剂咪唑克生(5微克/千克)经脑池内(i.c.)预处理可防止瑞米吉仑引起的MAP降低,但不能防止RSNA和HR降低。瑞米吉仑(300微克/千克,i.c.)可使MAP显著降低24%,RSNA降低32%,HR降低13%。咪唑克生(1微克/千克,i.c.)预处理可显著减弱瑞米吉仑的降压和交感抑制作用,而与IR结合不佳的α2 -拮抗剂育亨宾等摩尔至10倍高剂量的i.c.预处理则不能。然而,咪唑克生和育亨宾均未影响瑞米吉仑引起的心动过缓。我们得出结论:(a)瑞米吉仑经i.c.注射时比经i.v.注射表现出更显著的降压作用;(b)静脉注射的瑞米吉仑对RSNA的部分抑制作用可能通过咪唑克生不敏感的机制发挥,这些机制可能由药物的外周作用激活;(c)瑞米吉仑的降压作用与IR的相互作用比与α2 -肾上腺素能受体的相互作用更相关。

相似文献

1
Sympathoinhibitory action of rilmenidine in conscious sinoaortically denervated rats.利美尼定对清醒去窦主动脉神经大鼠的交感抑制作用。
J Cardiovasc Pharmacol. 1993 Aug;22(2):314-20. doi: 10.1097/00005344-199308000-00022.
2
Rilmenidine-induced hypotension in conscious rabbits involves imidazoline-preferring receptors.利美尼定引起清醒家兔低血压涉及咪唑啉优先受体。
J Cardiovasc Pharmacol. 1994 Jan;23(1):42-50. doi: 10.1097/00005344-199401000-00006.
3
[The effect of rilmenidine on the sympathetic activity of the renal nerve in waking barodenervated rats].
Eksp Klin Farmakol. 1993 Nov-Dec;56(6):19-21.
4
Involvement of imidazoline receptors in the baroreflex effects of rilmenidine in conscious rabbits.咪唑啉受体参与利美尼定对清醒家兔压力反射的作用。
J Hypertens. 2001 Sep;19(9):1615-24. doi: 10.1097/00004872-200109000-00014.
5
Renal effects of infusion of rilmenidine and guanabenz in conscious dogs: contribution of peripheral and central nervous system alpha 2-adrenoceptors.利美尼定和胍那苄输注对清醒犬的肾脏影响:外周和中枢神经系统α2-肾上腺素能受体的作用
Br J Pharmacol. 1995 Sep;116(1):1557-70. doi: 10.1111/j.1476-5381.1995.tb16373.x.
6
Involvement of imidazoline-preferring receptors in regulation of sympathetic tone.咪唑啉优先受体参与交感神经张力的调节。
Am J Cardiol. 1994 Dec 22;74(13):7A-19A. doi: 10.1016/0002-9149(94)90036-1.
7
Contribution of imidazoline receptors and alpha2-adrenoceptors in the rostral ventrolateral medulla to sympathetic baroreflex inhibition by systemic rilmenidine.延髓头端腹外侧部的咪唑啉受体和α2-肾上腺素能受体在瑞米吉仑全身性抑制交感压力反射中的作用
J Hypertens. 2007 Jan;25(1):147-55. doi: 10.1097/HJH.0b013e3280105ef0.
8
Sympathoinhibition by rilmenidine in conscious rabbits: involvement of alpha 2-adrenoceptors.利美尼定对清醒家兔的交感神经抑制作用:α2肾上腺素能受体的参与
Naunyn Schmiedebergs Arch Pharmacol. 1993 Dec;348(6):593-600. doi: 10.1007/BF00167235.
9
Sympathoinhibitory effects of rilmenidine may be mediated by sites located below the brainstem.利美尼定的交感神经抑制作用可能由位于脑干以下的部位介导。
Br J Pharmacol. 1992 Mar;105(3):535-41. doi: 10.1111/j.1476-5381.1992.tb09015.x.
10
Role of I1 imidazoline receptors in the sympathoinhibition produced by intracisternally administered rilmenidine and moxonidine.I1咪唑啉受体在脑池内注射利美尼定和莫索尼定产生的交感神经抑制中的作用。
Arzneimittelforschung. 1997 Sep;47(9):1009-15.

引用本文的文献

1
Drugs acting on imidazoline receptors: a review of their pharmacology, their use in blood pressure control and their potential interest in cardioprotection.作用于咪唑啉受体的药物:药理学综述、在血压控制中的应用及在心脏保护方面的潜在意义
Drugs. 1999 Nov;58(5):799-812. doi: 10.2165/00003495-199958050-00003.
2
Antiarrhythmic action of rilmenidine on adrenaline-induced arrhythmia via central imidazoline receptors in halothane-anaesthetized dogs.瑞米吉仑通过氟烷麻醉犬的中枢咪唑啉受体对肾上腺素诱发的心律失常的抗心律失常作用。
Br J Pharmacol. 1996 Apr;117(8):1744-8. doi: 10.1111/j.1476-5381.1996.tb15348.x.