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钾通道开放药物诱导的气管舒张:肾上腺素能神经元阻断剂对其的拮抗作用。

Tracheal relaxation induced by potassium channel opening drugs: its antagonism by adrenergic neurone blocking agents.

作者信息

Berry J L, Small R C, Foster R W

机构信息

Smooth Muscle Research Group, Department of Physiological Sciences, University of Manchester.

出版信息

Br J Pharmacol. 1992 Aug;106(4):813-8. doi: 10.1111/j.1476-5381.1992.tb14417.x.

DOI:10.1111/j.1476-5381.1992.tb14417.x
PMID:1393280
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1907678/
Abstract
  1. We have studied the ability of some adrenergic neurone blocking agents to inhibit the tracheal relaxant actions of isoprenaline, theophylline and the potassium channel openers (KCOs) BRL 38227, pinacidil and RP 52891. 2. BRL 38227, isoprenaline, pinacidil, RP 52891 and theophylline each caused concentration-dependent suppression of the spontaneous tone of guinea-pig isolated trachealis. The maximal relaxant effects of isoprenaline and pinacidil were equal to that of theophylline. In contrast, the maximal effects of BRL 38227 and RP 52891 were approximately 85-95% of that of theophylline. 3. Guanethidine (5-500 microM) did not itself modify the spontaneous tone of the trachealis muscle but antagonized BRL 38227 in a concentration-dependent manner. Guanethidine (50 microM) also antagonized pinacidil and RP 52891. However, guanethidine did not antagonize either isoprenaline or theophylline. 4. Bretylium (50 microM) did not itself modify the spontaneous tone of the trachealis muscle but antagonized BRL 38227, pinacidil and RP 52891. Bretylium did not antagonize either isoprenaline or theophylline. 5. Guanidine (50 and 500 microM) did not itself modify the spontaneous tone of the trachea and failed to modify the tracheal relaxant activity both of BRL 38227 and theophylline. 6. BRL 38227 (1 and 10 microM) stimulated, in a concentration-dependent manner, the efflux of 86Rb+ from strips of bovine trachealis muscle that had been pre-loaded with the radiotracer. Guanethidine (50 microM), bretylium (50 microM) and debrisoquine (50 microM) did not themselves modify the efflux of 86Rb+ from bovine trachealis but each of these agents markedly inhibited the stimulant effect of BRL 38227 (10 microM) on 86Rb+ efflux.7. It is concluded that the adrenergic neurone blocking agents guanethidine and bretylium can inhibit the tracheal relaxant actions of KCOs such as BRL 38227, pinacidil and RP 52891 without antagonizing isoprenaline or theophylline. The ability of the adrenergic neurone blocking agents to antagonize BRL 38227 in promoting 86Rb+ efflux from trachealis muscle may suggest that the adrenergic neurone blocking agents act to prevent the opening of the plasmalemmal K+-channel that is involved in the tracheal relaxant actions of the KCOs.
摘要
  1. 我们研究了一些肾上腺素能神经元阻断剂抑制异丙肾上腺素、茶碱以及钾通道开放剂(KCOs)BRL 38227、吡那地尔和RP 52891所致气管舒张作用的能力。2. BRL 38227、异丙肾上腺素、吡那地尔、RP 52891和茶碱均可引起豚鼠离体气管自发张力的浓度依赖性抑制。异丙肾上腺素和吡那地尔的最大舒张效应与茶碱的相等。相比之下,BRL 38227和RP 52891的最大效应约为茶碱的85 - 95%。3. 胍乙啶(5 - 500微摩尔)本身并不改变气管肌的自发张力,但以浓度依赖性方式拮抗BRL 38227。胍乙啶(50微摩尔)也拮抗吡那地尔和RP 52891。然而,胍乙啶并不拮抗异丙肾上腺素或茶碱。4. 溴苄铵(50微摩尔)本身并不改变气管肌的自发张力,但拮抗BRL 38227、吡那地尔和RP 52891。溴苄铵并不拮抗异丙肾上腺素或茶碱。5. 胍(50和500微摩尔)本身并不改变气管的自发张力,也不能改变BRL 38227和茶碱的气管舒张活性。6. BRL 38227(1和10微摩尔)以浓度依赖性方式刺激预先用放射性示踪剂加载的牛气管肌条中86Rb +的流出。胍乙啶(50微摩尔)、溴苄铵(50微摩尔)和异喹胍(50微摩尔)本身并不改变牛气管中86Rb +的流出,但这些药物中的每一种都显著抑制了BRL 38227(10微摩尔)对86Rb +流出的刺激作用。7. 得出的结论是,肾上腺素能神经元阻断剂胍乙啶和溴苄铵可抑制KCOs如BRL 38227、吡那地尔和RP 52891的气管舒张作用,而不拮抗异丙肾上腺素或茶碱。肾上腺素能神经元阻断剂拮抗BRL 38227促进气管肌中86Rb +流出的能力可能表明,肾上腺素能神经元阻断剂的作用是阻止参与KCOs气管舒张作用的质膜钾通道的开放。

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引用本文的文献

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Beta-adrenoceptor subtypes and the opening of plasmalemmal K(+)-channels in bovine trachealis muscle: studies of mechanical activity and ion fluxes.β-肾上腺素能受体亚型与牛气管平滑肌质膜钾通道的开放:机械活动和离子通量的研究
Br J Pharmacol. 1993 Aug;109(4):1149-56. doi: 10.1111/j.1476-5381.1993.tb13742.x.

本文引用的文献

1
Evidence that the spasmogenic action of tetraethylammonium in guinea-pig trachealis is both direct and dependent on the cellular influx of calcium ion.有证据表明,四乙铵对豚鼠气管平滑肌的致痉作用既是直接的,又依赖于钙离子的细胞内流。
Br J Pharmacol. 1983 May;79(1):255-63. doi: 10.1111/j.1476-5381.1983.tb10519.x.
2
Guanethidine effects on the guinea pig vas deferens are antagonized by the blockers of calcium-activated potassium conductance, apamin, methylene blue, and quinine.胍乙啶对豚鼠输精管的作用可被钙激活钾通道阻滞剂蜂毒明肽、亚甲蓝和奎宁所拮抗。
Mol Pharmacol. 1983 Mar;23(2):409-16.
3
An uptake of radioactivity from (plus or minus)-3H-isoprenaline and its inhibition by drugs which potentiate the responses to (minus)-isoprenaline in the guinea-pig isolated trachea.豚鼠离体气管对(±)-3H-异丙肾上腺素的放射性摄取及其对增强(-)-异丙肾上腺素反应的药物的抑制作用。
Br J Pharmacol. 1969 Mar;35(3):418-27. doi: 10.1111/j.1476-5381.1969.tb08283.x.
4
Inhibitory responses to nicotine and transmural stimulation in hyoscine-treated guinea-pig isolated trachealis: an electrical and mechanical study.东莨菪碱处理的豚鼠离体气管对尼古丁和跨壁刺激的抑制反应:电生理和力学研究
Br J Pharmacol. 1987 Apr;90(4):733-44. doi: 10.1111/j.1476-5381.1987.tb11227.x.
5
Intracellular bretylium blocks Na+ and K+ currents in heart cells.细胞内的溴苄铵可阻断心脏细胞中的钠电流和钾电流。
Eur J Pharmacol. 1988 Jul 14;151(3):389-97. doi: 10.1016/0014-2999(88)90535-3.
6
Cromakalim-induced relaxation of guinea-pig isolated trachealis: antagonism by glibenclamide and by phentolamine.克罗卡林诱导的豚鼠离体气管舒张:格列本脲和酚妥拉明的拮抗作用。
Br J Pharmacol. 1989 Nov;98(3):865-74. doi: 10.1111/j.1476-5381.1989.tb14615.x.
7
Potassium channel blockade: A mechanism for suppressing ventricular fibrillation.钾通道阻滞:一种抑制心室颤动的机制。
Proc Natl Acad Sci U S A. 1986 Apr;83(7):2223-7. doi: 10.1073/pnas.83.7.2223.
8
The action of a potassium channel activator, BRL 38227 (lemakalim), on human airway smooth muscle.
Am Rev Respir Dis. 1990 Dec;142(6 Pt 1):1384-9. doi: 10.1164/ajrccm/142.6_Pt_1.1384.
9
Characterization of responses to cromakalim and pinacidil in smooth and cardiac muscle by use of selective antagonists.使用选择性拮抗剂对平滑肌和心肌中对克罗卡林和吡那地尔的反应进行表征。
Br J Pharmacol. 1990 Jun;100(2):201-6. doi: 10.1111/j.1476-5381.1990.tb15782.x.
10
Glibenclamide blocks the relaxant action of pinacidil and cromakalim in airway smooth muscle.
Eur J Pharmacol. 1990 May 16;180(2-3):291-6. doi: 10.1016/0014-2999(90)90312-t.