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催产素对大鼠离体主动脉条收缩反应及45钙运动的影响。

The effect of oxytocin on contractile responses and 45Ca movements in rat isolated aortic strips.

作者信息

Barrigón S, Tamargo J

出版信息

Br J Pharmacol. 1986 Apr;87(4):763-70. doi: 10.1111/j.1476-5381.1986.tb14595.x.

Abstract

The effects of oxytocin (Oxt) on contractile responses and transmembrane Ca fluxes were studied in rat isolated aortic strips. Oxt (50-1000 mu ml-1) induced a dose-dependent contractile response and spontaneous myogenic activity. The Oxt-induced contractile response was not inhibited by pretreatment of aortic strips with phentolamine plus practolol, atropine, diphenhydramine plus cimetidine or indomethacin, but was significantly reduced by verapamil or deamino-ethyl-Oxt. The dose-response curve for Oxt was shifted upwards and to the left by increasing the Ca concentration of the medium from 1.8 to 4 mM. Oxt also shifted upwards the dose-response curve to Ca (1 to 5 mM) in aortic strips incubated in K depolarizing Ca-free media. Oxt increased the La3+-resistant 45Ca content without altering 45Ca efflux. The present results suggest that in rat isolated aortic strips Oxt produces a contractile response which, as previously found with other neurotransmitters, can be partly attributed to an increase of Ca influx through receptor-operated channels and to the release of Ca from intracellular stores.

摘要

在大鼠离体主动脉条上研究了催产素(Oxt)对收缩反应和跨膜钙通量的影响。Oxt(50 - 1000 μml-1)诱导剂量依赖性收缩反应和自发性肌源性活动。用酚妥拉明加心得宁、阿托品、苯海拉明加西咪替丁或吲哚美辛预处理主动脉条,不能抑制Oxt诱导的收缩反应,但维拉帕米或脱氨基乙基 - Oxt可使其显著降低。通过将培养基中的钙浓度从1.8 mM增加到4 mM,Oxt的剂量反应曲线向上和向左移动。在钾去极化无钙培养基中孵育的主动脉条中,Oxt也使对钙(1至5 mM)的剂量反应曲线向上移动。Oxt增加了抗镧3 +的45Ca含量,而不改变45Ca外流。目前的结果表明,在大鼠离体主动脉条中,Oxt产生收缩反应,正如先前在其他神经递质中发现的那样,这部分可归因于通过受体操纵通道的钙内流增加以及细胞内钙库中钙的释放。

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本文引用的文献

1
Changes in the vascular responses of the rat during pregnancy.大鼠孕期血管反应的变化。
J Physiol. 1959 Dec;149(3):586-92. doi: 10.1113/jphysiol.1959.sp006362.
2
ANTIARRHYTHMIC AND CARDIOVASCULAR EFFECTS OF SYNTHETIC OXYTOCIN.合成催产素的抗心律失常和心血管作用
Anesthesiology. 1964 Sep-Oct;25:653-61. doi: 10.1097/00000542-196409000-00013.
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Drugs that modify actions of pharmacologically active polypeptides.改变药理活性多肽作用的药物。
Ann N Y Acad Sci. 1963 Feb 4;104:281-9. doi: 10.1111/j.1749-6632.1963.tb17673.x.

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