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克罗卡林对豚鼠胃环形平滑肌收缩及膜电位的影响。

Effects of cromakalim on the contraction and the membrane potential of the circular smooth muscle of guinea-pig stomach.

作者信息

Ito K, Kanno T, Suzuki K, Masuzawa-Ito K, Takewaki T, Ohashi H, Asano M, Suzuki H

机构信息

Department of Veterinary Pharmacology, Faculty of Agriculture, Miyazaki University, Japan.

出版信息

Br J Pharmacol. 1992 Feb;105(2):335-40. doi: 10.1111/j.1476-5381.1992.tb14255.x.

Abstract
  1. The effects of cromakalim on mechanical and electrical activities of the circular smooth muscles of guinea-pig stomach antrum were observed. 2. Cromakalim (greater than 1 x 10(-7) M) decreased the amplitude of spontaneous rhythmic contractions and also the acetylcholine-enhanced spontaneous contractions. Cromakalim was less effective against the 25.9 mM and 35.9 mM K(+)-induced tonic contractions. 3. Glibenclamide (1 x 10(-6) M) itself caused no detectable change in the spontaneous contractions, those potentiated by acetylcholine or tonic contractions induced by high K+ solutions, but attenuated the actions of cromakalim. On the other hand, charybdotoxin (3 x 10(-8) M) increased the amplitude of spontaneous contractions but failed to affect the actions of cromakalim. 4. Cromakalim (greater than 1 x 10(-6) M) decreased the amplitude and duration of slow waves, and hyperpolarized the membrane. These actions of cromakalim were completely antagonized by 1 x 10(-6) M glibenclamide, whereas part of the effects of cromakalim on mechanical activity was resistant to glibenclamide. 5. The results suggest that the inhibition by cromakalim of the electrical activity and the hyperpolarization, which may be associated with the opening of glibenclamide-sensitive K+ channel, are responsible for its inhibitory action on circular smooth muscle of guinea-pig stomach. Further, some effects independent of glibenclamide-sensitive K+ channel may also be responsible for the mechanical effect.
摘要
  1. 观察了克罗卡林对豚鼠胃窦环行平滑肌机械活动和电活动的影响。2. 克罗卡林(大于1×10⁻⁷M)可降低自发性节律性收缩的幅度以及乙酰胆碱增强的自发性收缩幅度。克罗卡林对25.9 mM和35.9 mM钾离子诱导的强直性收缩作用较弱。3. 格列本脲(1×10⁻⁶M)本身对自发性收缩、乙酰胆碱增强的收缩或高钾溶液诱导的强直性收缩均未引起可检测到的变化,但可减弱克罗卡林的作用。另一方面,大蝎毒素(3×10⁻⁸M)可增加自发性收缩的幅度,但未能影响克罗卡林的作用。4. 克罗卡林(大于1×10⁻⁶M)可降低慢波的幅度和持续时间,并使膜超极化。克罗卡林的这些作用可被1×10⁻⁶M格列本脲完全拮抗,而克罗卡林对机械活动的部分作用对格列本脲具有抗性。5. 结果表明,克罗卡林对电活动的抑制作用和超极化作用可能与格列本脲敏感钾通道的开放有关,这是其对豚鼠胃环行平滑肌产生抑制作用的原因。此外,一些独立于格列本脲敏感钾通道的作用也可能是其产生机械效应的原因。

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