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多巴胺对离体豚鼠回肠胆碱能传递的抑制作用。通过α-肾上腺素能受体介导。

The inhibition by dopamine of cholinergic transmission in the isolated guinea-pig ileum. Mediation through alpha-adrenoceptors.

作者信息

Görich R, Weihrauch T R, Kilbinger H

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1982 Mar;318(4):308-12. doi: 10.1007/BF00501170.

Abstract
  1. Segments of the guinea-pig ileum were incubated in Tyrode's solution containing 3 microM propranolol. Dopamine, like noradrenaline and clonidine, inhibited the twitch response to field stimulation. The inhibitory action of dopamine remained unchanged in the presence of the dopamine uptake inhibitor nomifensine (1 microM). Tissue from reserpine-pretreated animals was insensitive to tyramine but the response to dopamine was not affected. It is, therefore, assumed that the effect of dopamine is due to a direct receptor stimulation and not to the release of noradrenaline. 2. The inhibitory action of dopamine was not antagonized by the dopamine receptor antagonists cis-flupenthixol, pimozide or domperidone. 3. Metoclopramide, sulpiride and tolazoline were competitive antagonists of the inhibitory effects of dopamine. The pA2-values for metoclopramide against dopamine (5.64), noradrenaline (5.52), and clonidine (5.57) did not differ significantly. Likewise, there was no significant difference between the pA2-values for sulpiride (5.30, 5.29, 5.50) and those for tolazoline (6.52, 6.69, 7.02) determined against dopamine, noradrenaline and clonidine. 4. Apomorphine inhibited the twitch response, and this inhibition was not affected by tolazoline, sulpiride or pimozide. 5. It is concluded that dopamine inhibits the twitch response in the guinea-pig ileum through stimulation of neuronal alpha-adrenoceptors. Metoclopramide and sulpiride are weak antagonists at these receptors. The results provide no evidence for the existence of specific inhibitory dopamine receptors in the guinea-pig ileum.
摘要
  1. 将豚鼠回肠段置于含有3微摩尔普萘洛尔的台氏液中孵育。多巴胺与去甲肾上腺素和可乐定一样,抑制对场刺激的抽搐反应。在存在多巴胺摄取抑制剂诺米芬辛(1微摩尔)的情况下,多巴胺的抑制作用保持不变。来自利血平预处理动物的组织对酪胺不敏感,但对多巴胺的反应不受影响。因此,推测多巴胺的作用是由于直接刺激受体,而不是由于去甲肾上腺素的释放。2. 多巴胺受体拮抗剂顺式氟哌噻吨、匹莫齐特或多潘立酮不能拮抗多巴胺的抑制作用。3. 甲氧氯普胺、舒必利和妥拉唑啉是多巴胺抑制作用的竞争性拮抗剂。甲氧氯普胺对多巴胺(5.64)、去甲肾上腺素(5.52)和可乐定(5.57)的pA2值无显著差异。同样,舒必利(5.30、5.29、5.50)和妥拉唑啉(6.52、6.69、7.02)对多巴胺、去甲肾上腺素和可乐定的pA2值也无显著差异。4. 阿扑吗啡抑制抽搐反应,且这种抑制不受妥拉唑啉、舒必利或匹莫齐特的影响。5. 结论是多巴胺通过刺激神经元α-肾上腺素能受体抑制豚鼠回肠的抽搐反应。甲氧氯普胺和舒必利是这些受体的弱拮抗剂。结果没有提供豚鼠回肠中存在特异性抑制性多巴胺受体的证据。

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