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某些血管活性多肽及其拮抗剂对肛尾肌的作用。

The actions of some vasoactive polypeptides and their antagonists on the anococcygeus muscle.

作者信息

Gillespie J S, McKnight A T

出版信息

Br J Pharmacol. 1978 Feb;62(2):267-74. doi: 10.1111/j.1476-5381.1978.tb08455.x.

Abstract

1 The action of three polypeptides, bradykinin, substance P and eledoisin known to inhibit vascular smooth muscle has been examined on the anococcygeus muscle of the rat, cat and rabbit.2 In the atonic rat muscle, bradykinin and substance P had little or no effect on tone but eledoisin produced a sustained dose-related contraction which could be abolished by phentolamine (1 muM) and is, therefore, probably an indirect sympathomimetic effect. On the motor response to field stimulation of adrenergic nerves, bradykinin had no effect whereas both substance P and eledoisin reduced this response. The mechanism of action was further analysed with eledoisin by examining its effect on the response to noradrenaline. Eledoisin did not alter the dose-response curve to noradrenaline and its inhibitory action is likely, therefore, to be presynaptic.3 In the rat anococcygeus muscle in which the tone was raised by guanethidine or carbachol, bradykinin and substance P reduced this tone whereas eledoisin continued to exert a motor action. Compared with substance P the inhibitory effect of bradykinin appeared at lower concentrations (threshold 0.01 mug/ml), developed more rapidly and the size of the response was greater.4 The effect of bradykinin on the tonically contracted cat and rabbit anococcygeus muscles was examined in addition to that of the rat. In all three species bradykinin caused inhibition and the magnitude of the response was equal to the maximum effect of inhibitory nerve stimulation. None of the peptides affected the inhibitory response to nerve stimulation itself.5 The effects of three substances, hesperitin, khellin and apiin, reported in other tissues to antagonize the action of bradykinin were examined both on the inhibitory response to bradykinin and to field stimulation. None of them was able to inhibit either response, although they reduced tone when given by themselves. During these experiments it was found that ethanol antagonized the inhibitory response to field stimulation.6 The possibility that bradykinin or some related peptide might play a part in the inhibitory response to nerve stimulation in the anococcygeus is discussed.

摘要
  1. 已经在大鼠、猫和兔的肛门尾骨肌上研究了三种已知可抑制血管平滑肌的多肽——缓激肽、P物质和伊索辛的作用。

  2. 在张力缺失的大鼠肌肉中,缓激肽和P物质对张力几乎没有影响,但伊索辛产生持续的剂量相关收缩,这种收缩可被酚妥拉明(1μM)消除,因此,可能是一种间接拟交感神经效应。关于对肾上腺素能神经场刺激的运动反应,缓激肽没有作用,而P物质和伊索辛都降低了这种反应。通过检查伊索辛对去甲肾上腺素反应的影响,进一步分析了其作用机制。伊索辛没有改变对去甲肾上腺素的剂量反应曲线,因此其抑制作用可能是突触前的。

  3. 在通过胍乙啶或卡巴胆碱使张力升高的大鼠肛门尾骨肌中,缓激肽和P物质降低了这种张力,而伊索辛继续发挥运动作用。与P物质相比,缓激肽的抑制作用在较低浓度(阈值0.01μg/ml)时出现,发展更快,反应幅度更大。

  4. 除了大鼠,还研究了缓激肽对张力性收缩的猫和兔肛门尾骨肌的影响。在所有三个物种中,缓激肽都引起抑制,反应幅度等于抑制性神经刺激的最大效应。这些肽均不影响对神经刺激本身的抑制反应。

  5. 研究了橙皮素、凯林和芹菜苷这三种在其他组织中据报道可拮抗缓激肽作用的物质对缓激肽抑制反应和场刺激的影响。它们均不能抑制任何一种反应,尽管它们单独给药时可降低张力。在这些实验过程中发现,乙醇可拮抗对场刺激的抑制反应。

  6. 讨论了缓激肽或某些相关肽可能在肛门尾骨肌对神经刺激的抑制反应中起作用的可能性。

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Sympathetic postganglionic cholinergic fibres.交感神经节后胆碱能纤维。
Br J Pharmacol Chemother. 1960 Mar;15(1):56-66. doi: 10.1111/j.1476-5381.1960.tb01210.x.

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