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钙拮抗剂与大鼠输精管及豚鼠回肠平滑肌的收缩反应

Calcium antagonists and contractile responses in rat vas deferens and guinea pig ileal smooth muscle.

作者信息

Triggle C R, Swamy V C, Triggle D J

出版信息

Can J Physiol Pharmacol. 1979 Aug;57(8):804-18. doi: 10.1139/y79-124.

Abstract

The effect of depletion of extracellular Ca2+ (Ca2+ext) on the loss of responsiveness of the guinea pig ileal longitudinal muscle (g.p.i.l.m.) and the rat vas deferens (r.v.d.) to K+ and cis-2-methyl-4-dimethylaminomethyl-1,3-dioxolane methiodide (CD), and K+ and noradrenaline (NA), has been examined and compared with the effects of a variety of local anesthetics and calcium antagonists. The results indicate that qualitative similarities are apparent with respect to the dependence of agonist-induced activity on Ca2+ext in both the g.p.i.l.m. and r.v.d. Distinct differences, however, in the Ca2+ translocation processes in these two tissues, in response to the different agonists, can be shown by the use of a variety of 'calcium antagonists' thus indicating that such translocation processes are both tissue and agonist selective. It is thus noted that, contrary to the Ca2+ depletion studies, D 600 and the usually more potent BAY-1040 showed no discrimination of action or potency in their ability to inhibit components of the NA response in the r.v.d. In contrast, D 600 and the more potent BAY-1040 selectively inhibited the tonic component of the K+ response. Treatment with SKF 525A and parethoxycaine (PC) in the g.p.i.l.m. and SKF 525A in the r.v.d. resulted in a nonselective inhibition of responses of the tissues to all stimulants. However, in the r.v.d. PC potentiated NA action, and its methobromide (MeBr) derivative potentiated both NA and K+ action and also, like PC, partially shifted to the left the dose-response curve to Ca2+ in NA-depolarizing Ca-free Tyrode's. The quaternary MeBr and the tertiary 2-chloroethyl (2Cl) derivatives of SKF 525A and PC were selectively more effective against CD- than K+ supported contractile activity in the g.p.i.l.m. and the 2Cl derivatives were more effective against NA than K+ responses in the r.v.d. The 2Cl derivative of PC also was more effective in antagonizing the Ca2+ dose-response curve in high-CD or high-NA than in high-K+ Ca2+-free Tyrode's.

摘要

研究了细胞外钙离子(Ca2+ext)耗竭对豚鼠回肠纵肌(g.p.i.l.m.)和大鼠输精管(r.v.d.)对钾离子(K+)和顺式-2-甲基-4-二甲基氨基甲基-1,3-二氧戊环甲碘化物(CD)以及K+和去甲肾上腺素(NA)反应性丧失的影响,并与多种局部麻醉药和钙拮抗剂的作用进行了比较。结果表明,在g.p.i.l.m.和r.v.d.中,激动剂诱导的活性对Ca2+ext的依赖性在性质上具有明显的相似性。然而,通过使用多种“钙拮抗剂”可以显示,这两种组织中针对不同激动剂的Ca2+转运过程存在明显差异,这表明这种转运过程具有组织和激动剂选择性。因此需要注意的是,与Ca2+耗竭研究相反,D 600和通常更有效的BAY-1040在抑制r.v.d.中NA反应成分的能力方面没有表现出作用或效力的差异。相比之下,D 600和更有效的BAY-1040选择性地抑制了K+反应的张力成分。在g.p.i.l.m.中用SKF 525A和对乙氧基卡因(PC)处理以及在r.v.d.中用SKF 525A处理,导致组织对所有刺激的反应受到非选择性抑制。然而,在r.v.d.中,PC增强了NA的作用,其甲溴化物(MeBr)衍生物增强了NA和K+的作用,并且与PC一样,在无钙的NA去极化Tyrode溶液中,部分将Ca2+的剂量反应曲线向左移动。SKF 525A和PC的季铵盐MeBr和叔氯乙基(2Cl)衍生物在g.p.i.l.m.,中对CD支持的收缩活性比对K+支持的收缩活性选择性更有效,而2Cl衍生物在r.v.d.中对NA反应比对K+反应更有效。PC的2Cl衍生物在高CD或高NA条件下比在高K+无钙Tyrode溶液中更有效地拮抗Ca2+剂量反应曲线。

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