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豚鼠回肠纵肌中通过组胺H1受体,毒蕈碱M2刺激对收缩机制的抑制作用。

Suppression by muscarinic M2 stimulation of the contractile mechanism via histamine H1 receptors in the longitudinal muscle of guinea pig ileum.

作者信息

Ishii K, Kato R

出版信息

J Pharmacol Exp Ther. 1987 May;241(2):587-93.

PMID:3553541
Abstract

The longitudinal muscle of the guinea pig ileum is well known to contract in response to stimulation of either muscarinic or histamine H1 receptors. However, we found that simultaneous application of agonists to both receptors, methacholine (MeCh) and histamine (Hist), at their maximum concentrations (both at 10(-5) M), induced a contraction of the muscle with a pattern very similar to that observed with MeCh alone. In the muscle contracted by MeCh, a muscarinic antagonist, atropine, caused a transient relaxation, but a histamine H1 blocker, pyrilamine, had no effect on the tension. Experiments using pirenzepine indicated that muscarinic-M1 receptors did not seem to be involved in the mechanism of this phenomenon. The atropine-induced relaxation was not affected by phentolamine (10(-6) M), propranolol (10(-6) M) or tetrodotoxin (10(-6) M). After pretreatment of the muscle with 10(-5) M MeCh for 10 min, the contractile effect of 10(-5) M Hist was suppressed intensely for a certain time period, but that of 10(-5) M MeCh was not diminished. On the other hand, pretreatment of the muscle with 10(-5) M Hist for 10 min did not influence the contraction by either MeCh or Hist. The suppression by MeCh of the Hist action developed dependently on the concentration of MeCh and the time length of exposure to MeCh, and the persistence was temperature-dependent. Furthermore, this suppression was not surmounted by the elevation of Hist concentration. A similar phenomenon was also observed in the muscle which was immersed in the nutrient solution without CaCl2.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

豚鼠回肠的纵行肌因毒蕈碱或组胺H1受体受刺激而收缩是众所周知的。然而,我们发现同时以最大浓度(均为10⁻⁵ M)向两种受体施加激动剂,即乙酰甲胆碱(MeCh)和组胺(Hist),会诱导肌肉收缩,其模式与单独使用MeCh时观察到的非常相似。在由MeCh收缩的肌肉中,毒蕈碱拮抗剂阿托品会引起短暂的松弛,但组胺H1阻滞剂吡苄明对张力没有影响。使用哌仑西平的实验表明,毒蕈碱-M1受体似乎不参与这一现象的机制。阿托品诱导的松弛不受酚妥拉明(10⁻⁶ M)、普萘洛尔(10⁻⁶ M)或河豚毒素(10⁻⁶ M)的影响。用10⁻⁵ M MeCh预处理肌肉10分钟后,10⁻⁵ M Hist的收缩作用在一定时间段内被强烈抑制,但10⁻⁵ M MeCh的收缩作用并未减弱。另一方面,用10⁻⁵ M Hist预处理肌肉10分钟对MeCh或Hist引起的收缩均无影响。MeCh对Hist作用的抑制作用随MeCh浓度和暴露于MeCh的时间长度而发展,且持续性与温度有关。此外,这种抑制作用不会因Hist浓度升高而被克服。在浸入无CaCl₂营养液中的肌肉中也观察到了类似现象。(摘要截取自250字)

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