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乙酰胆碱和缓激肽对豚鼠回肠作用的比较。

A comparison of the actions of acetylcholine and bradykinin on the guinea pig ileum.

作者信息

Roberts M L

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1980 Nov;314(3):267-70. doi: 10.1007/BF00498548.

Abstract

Procaine (8.5 x 10(-5) M) inhibited the action of acetylcholine but not that of bradykinin on the guinea pig ileum. Attempts were made to identify the difference in stimulus-response coupling which would explain this difference in sensitivity. The responses to both agonists were dependent upon the presence of Ca2+ in the extracellular fluid, were inhibited to approximately the same extent by the addition of 0.25 mM Mn2+ to the bathing fluid and were equally sensitivity to reduction in Na+ concentration of the extracellular fluid. Neither acetylcholine nor bradykinin could provoke ileal contraction when Sr2+ was substituted for Ca2+. Thus there was no indication of the difference in the stimulus-response pathways for the two agonists which must exist to explain the differential sensitivity to procaine.

摘要

普鲁卡因(8.5×10⁻⁵ M)抑制乙酰胆碱对豚鼠回肠的作用,但不抑制缓激肽的作用。人们试图确定刺激-反应偶联中的差异,以解释这种敏感性差异。对两种激动剂的反应均依赖于细胞外液中Ca²⁺的存在,在浴液中加入0.25 mM Mn²⁺后,二者受到的抑制程度大致相同,并且对细胞外液中Na⁺浓度降低的敏感性相同。当用Sr²⁺替代Ca²⁺时,乙酰胆碱和缓激肽均不能引起回肠收缩。因此,没有迹象表明两种激动剂的刺激-反应途径存在差异,而这种差异必然存在才能解释对普鲁卡因的不同敏感性。

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