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运用计算机辅助视频显微镜技术对豚鼠回肠黏膜下小动脉中介导血管舒张的毒蕈碱受体进行表征。

Characterization of muscarinic receptors mediating vasodilation in guinea-pig ileum submucosal arterioles by the use of computer-assisted videomicroscopy.

作者信息

Bungardt E, Vockert E, Feifel R, Moser U, Tacke R, Mutschler E, Lambrecht G, Surprenant A

机构信息

Department of Pharmacology, University of Frankfurt, Germany.

出版信息

Eur J Pharmacol. 1992 Mar 17;213(1):53-61. doi: 10.1016/0014-2999(92)90232-s.

Abstract

Muscarinic receptors of resistance vessels (submucosal arterioles, outside diameter 50-75 microns) from the guinea-pig small intestine were investigated in vitro using a computer-assisted videomicroscopy system (Diamtrak). The muscarinic receptor which mediates vasodilation of precontracted [U-46619 (300 nM) or (-)-noradrenaline (10 microM)] arterioles was characterized with several muscarinic agonists and subtype-selective antagonists. The following agonists all produced equivalent maximum vasodilation (given in rank order of potency): acetylcholine = arecaidine propargyl ester (APE) greater than oxotremorine = (+/-)-muscarine = (+/-)-methacholine greater than carbachol greater than 4-[[N-(4-chlorophenyl)carbamoyl]oxy]-2-butynyltrimethylammonium iodide (4-Cl-McN-A-343). 4-[[N-(3-Chlorophenyl)-carbamoyl]oxy]-2-butynyltrimethylammonium chloride (McN-A-343) and N-ethyl-guvacine propargyl ester (NEN-APE) produced minimal or no arteriolar vasodilation. The muscarinic antagonists pirenzepine, (+-)-5,11-dihydro-11-[[[2-[2-((dipropylamino)methyl)-1-piperidinyl] ethyl]amino]-carbonyl]-6H-pyrido(2,3-b)(1,4)-benzodiazepin-6-one (AF-DX 384), 11-[[4-[4-(diethylamino)butyl]-1-piperidinyl]acetyl]-5,11-dihydro- 6H-pyrido(2,3-b)(1,4)-benzodiazepin-6-one (AQ-RA 741), p-fluorohexahydro-sila-difenidol (p-F-HHSiD), 4-diphenylacetoxy-N-methylpiperidine methiodide (4-DAMP) and (R)- and (S)-hexahydro-difenidol [(R)-HHD, (S)-HHD] shifted the muscarine, methacholine or carbachol dose-response curve to the right in a competitive manner. Schild analysis of the data yielded pA2 values for pirenzepine (6.74/6.9), AF-DX 384 (6.72), AQ-RA 741 (6.58), p-F-HHSiD (7.53/7.57), 4-DAMP (9.06), (R)-HHD (7.88/8.32) and (S)-HHD (5.52/5.88). Thus, it can be concluded that submucosal arterioles possess only the M3 functional muscarinic receptor, the activation of which causes blood vessel dilation.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

利用计算机辅助视频显微镜系统(Diamtrak)在体外研究了豚鼠小肠阻力血管(黏膜下小动脉,外径50 - 75微米)的毒蕈碱受体。用几种毒蕈碱激动剂和亚型选择性拮抗剂对介导预收缩的[U - 46619(300 nM)或( - ) - 去甲肾上腺素(10 microM)]小动脉血管舒张的毒蕈碱受体进行了表征。以下激动剂均产生等效的最大血管舒张作用(按效力顺序排列):乙酰胆碱 = 槟榔碱炔丙酯(APE)>氧化震颤素 = (±) - 毒蕈碱 = (±) - 醋甲胆碱>卡巴胆碱>4 - [[N - (4 - 氯苯基)氨基甲酰基]氧基] - 2 - 丁炔基三甲基碘化铵(4 - Cl - McN - A - 343)。4 - [[N - (3 - 氯苯基)氨基甲酰基]氧基] - 2 - 丁炔基三甲基氯化铵(McN - A - 343)和N - 乙基 - 古戊酰胺炔丙酯(NEN - APE)产生最小或无小动脉血管舒张作用。毒蕈碱拮抗剂哌仑西平、(±) - 5,11 - 二氢 - 11 - [[[2 - [2 - (二丙基氨基)甲基] - 1 - 哌啶基]乙基]氨基]羰基] - 6H - 吡啶并(2,3 - b)(1,4) - 苯二氮䓬 - 6 - 酮(AF - DX 384)、11 - [[4 - [4 - (二乙氨基)丁基] - ! - 哌啶基]乙酰] - 5,11 - 二氢 - 6H - 吡啶并(2,3 - b)(1,4) - 苯二氮䓬 - 6 - 酮(AQ - RA 741)、对氟六氢硅二苯醚(p - F - HHSiD)、4 - 二苯乙酰氧基 - N - 甲基哌啶甲碘化物(4 - DAMP)以及(R) - 和(S) - 六氢二苯醚[(R) - HHD,(S) - HHD]以竞争性方式使毒蕈碱、醋甲胆碱或卡巴胆碱的剂量 - 反应曲线右移。对数据进行Schild分析得出哌仑西平(6.74/6.9)、AF - DX 384(6.72)、AQ - RA 741(6.58)、p - F - HHSiD(7.53/7.57)、4 - DAMP(9.06)、(R) - HHD(7.88/8.32)和(S) - HHD(5.52/5.88)的pA2值。因此,可以得出结论,黏膜下小动脉仅具有M3功能性毒蕈碱受体,其激活会导致血管舒张。(摘要截短于250字)

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