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非肾上腺素能、非胆碱能神经刺激和外源性应用ATP对来自不同脊椎动物物种的多种平滑肌制剂的兴奋和抑制作用的比较。

A comparison of the excitatory and inhibitory effects of non-adrenergic, non-cholinergic nerve stimulation and exogenously applied ATP on a variety of smooth muscle preparations from different vertebrate species.

作者信息

Burnstock G, Satchell D G, Smythe A

出版信息

Br J Pharmacol. 1972 Oct;46(2):234-42. doi: 10.1111/j.1476-5381.1972.tb06868.x.

Abstract
  1. The responses to non-adrenergic, non-cholinergic nerve stimulation have been compared with those to exogenously applied ATP on seventeen different tissues from a number of vertebrate classes.2. Stimulation of all the mammalian gut preparations studied (with the exception of the guinea-pig ileum) after blockade of the effects of adrenergic and cholinergic nerve stimulation by guanethidine (3.5 muM) and hyoscine (1.3 muM) caused inhibition; exogenously applied ATP mimicked this inhibitory response.3. Stimulation of the guinea-pig ileum in the presence of hyoscine and guanethidine, usually caused a diphasic response, relaxation followed by contraction; exogenously applied ATP mimicked this response, in contrast to acetylcholine and noradrenaline which caused excitation and relaxation respectively.4. Stimulation of preparations of lower vertebrate gut and guinea-pig bladder in the presence of hyoscine and guanethidine caused contraction; exogenously applied ATP mimicked this contractile response.5. In each preparation the time course of the response to ATP was similar or identical to the response to non-adrenergic, non-cholinergic nerve stimulation.6. The results are consistent with the hypothesis that a purine nucleotide may be the transmitter substance released from non-adrenergic, non-cholinergic nerves supplying smooth muscle preparations from a number of vertebrate classes.
摘要
  1. 已将对非肾上腺素能、非胆碱能神经刺激的反应与对多种脊椎动物类别的17种不同组织外源性应用ATP的反应进行了比较。

  2. 在通过胍乙啶(3.5 μM)和东莨菪碱(1.3 μM)阻断肾上腺素能和胆碱能神经刺激的作用后,对所有研究的哺乳动物肠道制剂(豚鼠回肠除外)进行刺激会导致抑制;外源性应用ATP模拟了这种抑制反应。

  3. 在东莨菪碱和胍乙啶存在的情况下,对豚鼠回肠进行刺激通常会引起双相反应,先是松弛,然后是收缩;外源性应用ATP模拟了这种反应,这与分别引起兴奋和松弛的乙酰胆碱和去甲肾上腺素形成对比。

  4. 在东莨菪碱和胍乙啶存在的情况下,对低等脊椎动物肠道和豚鼠膀胱的制剂进行刺激会导致收缩;外源性应用ATP模拟了这种收缩反应。

  5. 在每种制剂中,对ATP的反应时间进程与对非肾上腺素能、非胆碱能神经刺激的反应相似或相同。

  6. 这些结果与以下假设一致,即嘌呤核苷酸可能是从为多种脊椎动物类别的平滑肌制剂提供神经支配的非肾上腺素能、非胆碱能神经释放的递质物质。

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本文引用的文献

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INHIBITION OF INTESTINAL SMOOTH MUSCLE.肠平滑肌的抑制
Aust J Exp Biol Med Sci. 1965 Jun;43:277-90. doi: 10.1038/icb.1965.27.
8
Secondary excitation of intestinal smooth muscle.肠道平滑肌的继发性兴奋
Br J Pharmacol. 1971 Feb;41(2):213-26. doi: 10.1111/j.1476-5381.1971.tb08023.x.

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