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儿茶酚胺对豚鼠食管黏膜下丛-纵行肌黏膜制备物电诱发收缩的抑制作用。

Inhibitory actions of catecholamines on electrically induced contractions of the submucous plexus-longitudinal muscularis mucosae preparation of the guinea-pig oesophagus.

作者信息

Kamikawa Y, Shimo Y, Uchida K

出版信息

Br J Pharmacol. 1982 Jun;76(2):271-7. doi: 10.1111/j.1476-5381.1982.tb09217.x.

Abstract

1 The submucous plexus-longitudinal muscularis mucosae preparation of the guinea-pig oesophagus was used to study the actions of catecholamines on the twitch responses to electrical stimulation.2 When the preparation was stimulated coaxially (0.1 Hz, 0.5 ms, supramaximal voltage), stable twitch-like contractions were obtained. These were abolished by tetrodotoxin (0.1 muM) and atropine (0.1 muM), potentiated by physostigmine (0.1 muM), and were mediated presumably by stimulation of intramural cholinergic nerves.3 The twitch contractions of the muscularis mucosae were inhibited by catecholamines, in a concentration-dependent manner. The order of potency was isoprenaline > adrenaline > noradrenaline > dopamine.4 The inhibitory actions of noradrenaline (1 muM) and adrenaline (1 muM) were partly reversed by phentolamine (1 muM) or by propranolol (1 muM), and completely abolished by both antagonists together. The inhibitory effect of dopamine (300 muM) was largely reversed by phentolamine (1 muM), but not by propranolol (1 muM), while the inhibitory action of isoprenaline was competitively antagonized only by propranolol (pA(2) of 7.6).5 The contraction of the muscularis mucosae to exogenously applied acetylcholine (ACh, 20 nM) which was comparable in magnitude with that to electrical stimulation was also inhibited by isoprenaline (0.1 muM), adrenaline (1 muM) and noradrenaline (1 muM), but not by dopamine (300 muM). In the presence of propranolol (1 muM), noradrenaline, adrenaline and dopamine potentiated the ACh-induced contraction, while the effect of isoprenaline was mainly antagonized. The potentiating effects were antagonized by further treatment with phentolamine (1 muM).6 Adrenaline, noradrenaline and dopamine but not isoprenaline, produced a weak contraction of the longitudinal muscularis mucosae in the presence of propranolol (3 muM). The contractile responses were completely inhibited by phentolamine (3 muM). Tone in the muscularis mucosae induced by carbachol (3 muM) in the presence of phentolamine (10 muM) was inhibited by catecholamines, in a concentration-dependent manner, an effect that was competitively antagonized by propranolol.7 In the submucous plexus-longitudinal muscularis mucosae preparation of the guinea-pig oesophagus there are three types of adrenoceptor, inhibitory prejunctional alpha-adrenoceptors, excitatory postjunctional alpha-adrenoceptors and inhibitory postjunctional beta-adrenoceptors, and cholinergic neurotransmission is inhibited by catecholamines acting at both prejunctional alpha- and postjunctional beta-adrenoceptors.

摘要
  1. 采用豚鼠食管黏膜下丛-纵行肌黏膜制备物,研究儿茶酚胺对电刺激引起的抽搐反应的作用。

  2. 当同轴刺激该制备物(0.1Hz,0.5ms,超最大电压)时,可获得稳定的类似抽搐的收缩。这些收缩被河豚毒素(0.1μM)和阿托品(0.1μM)消除,被毒扁豆碱(0.1μM)增强,推测是由刺激壁内胆碱能神经介导的。

  3. 儿茶酚胺以浓度依赖的方式抑制黏膜肌的抽搐收缩。效力顺序为异丙肾上腺素>肾上腺素>去甲肾上腺素>多巴胺。

  4. 去甲肾上腺素(1μM)和肾上腺素(1μM)的抑制作用部分被酚妥拉明(1μM)或普萘洛尔(1μM)逆转,两种拮抗剂共同作用则完全消除。多巴胺(300μM)的抑制作用大部分被酚妥拉明(1μM)逆转,但不被普萘洛尔(1μM)逆转,而异丙肾上腺素的抑制作用仅被普萘洛尔竞争性拮抗(pA₂为7.6)。

  5. 黏膜肌对体外施加的乙酰胆碱(ACh,20nM)的收缩,其幅度与对电刺激的收缩相当,也被异丙肾上腺素(0.1μM)、肾上腺素(1μM)和去甲肾上腺素(1μM)抑制,但不被多巴胺(300μM)抑制。在普萘洛尔(1μM)存在时,去甲肾上腺素、肾上腺素和多巴胺增强ACh诱导的收缩,而异丙肾上腺素的作用主要被拮抗。进一步用酚妥拉明(1μM)处理可拮抗增强作用。

  6. 在普萘洛尔(3μM)存在时,肾上腺素、去甲肾上腺素和多巴胺但不是异丙肾上腺素,引起纵行黏膜肌轻微收缩。收缩反应被酚妥拉明(3μM)完全抑制。在酚妥拉明(10μM)存在时,卡巴胆碱(3μM)诱导的黏膜肌张力被儿茶酚胺以浓度依赖的方式抑制,这种作用被普萘洛尔竞争性拮抗。

  7. 在豚鼠食管黏膜下丛-纵行肌黏膜制备物中存在三种肾上腺素能受体,抑制性节前α-肾上腺素能受体、兴奋性节后α-肾上腺素能受体和抑制性节后β-肾上腺素能受体,儿茶酚胺作用于节前α-和节后β-肾上腺素能受体均抑制胆碱能神经传递。

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