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α和β肾上腺素能受体在儿茶酚胺对肠道平滑肌某些作用中的角色。

The role of alpha- and beta- adrenergic receptors in some actions of catecholamines on intestinal smooth muscle.

作者信息

Jenkinson D H, Morton I K

出版信息

J Physiol. 1967 Feb;188(3):387-402. doi: 10.1113/jphysiol.1967.sp008145.

DOI:10.1113/jphysiol.1967.sp008145
PMID:6032206
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1396027/
Abstract
  1. Experiments were carried out to determine the type of adrenergic receptor concerned in the action of noradrenaline in increasing the rate of exchange of potassium ions in the taenia of the guinea-pig caecum. The preparations were bathed in potassium-rich solutions in order to depolarize the muscle fibres and so eliminate changes in potassium flux secondary to alterations in membrane potential.2. Noradrenaline was more effective than isoprenaline in increasing both the influx and efflux of (42)K, suggesting that the alpha-receptors were involved. This action on potassium permeability was abolished by the alpha-blocking agent phentolamine (10(-7) g/ml.), the beta-blocking agent pronethalol (10(-7) g/ml.) being without effect.3. In contrast, isoprenaline was about 30 times more active than noradrenaline in inhibiting calcium contractures of the depolarized taenia, suggesting that here the beta-receptors were concerned. This was confirmed by showing that this action of noradrenaline was effectively antagonized by pronethalol, again at 10(-7) g/ml., but not by the same concentration of phentolamine.4. Carbachol contractures in quiescent preparations bathed in Krebs solution at 17 degrees C could be inhibited by both noradrenaline and isoprenaline. Noradrenaline was found to be more active under these conditions, and this action was antagonized by phentolamine (and piperoxane), but not by pronethalol, at the same concentrations as before.5. These findings confirm that the alpha- and beta-receptors are quite distinct in their actions. Nevertheless, under physiological conditions, both may contribute to the inhibitory actions of catecholamines on intestinal smooth muscle.
摘要
  1. 进行了实验以确定去甲肾上腺素在增加豚鼠盲肠带中钾离子交换速率的作用中所涉及的肾上腺素能受体类型。将标本置于富含钾的溶液中浸泡,以使肌纤维去极化,从而消除继发于膜电位改变的钾通量变化。

  2. 去甲肾上腺素在增加(42)K的流入和流出方面比异丙肾上腺素更有效,表明涉及α受体。α受体阻断剂酚妥拉明(10(-7)g/ml)可消除这种对钾通透性的作用,而β受体阻断剂普萘洛尔(10(-7)g/ml)则无作用。

  3. 相比之下,异丙肾上腺素在抑制去极化带的钙挛缩方面比去甲肾上腺素活跃约30倍,表明此处涉及β受体。通过显示普萘洛尔(同样为10(-7)g/ml)可有效拮抗去甲肾上腺素的这种作用,但相同浓度的酚妥拉明则不能,证实了这一点。

  4. 在17℃的Krebs溶液中浸泡的静止标本中,卡巴胆碱挛缩可被去甲肾上腺素和异丙肾上腺素抑制。发现在这些条件下去甲肾上腺素更活跃,并且这种作用在与之前相同的浓度下可被酚妥拉明(和哌罗克生)拮抗,但不能被普萘洛尔拮抗。

  5. 这些发现证实α受体和β受体的作用截然不同。然而,在生理条件下,两者都可能有助于儿茶酚胺对肠道平滑肌的抑制作用。

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