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肾上腺素能受体介导的兔小肠和大肠反应。

Adrenergic receptor-mediated response of the rabbit small and large intestine.

作者信息

Sim M K, Lim J M

出版信息

Jpn J Pharmacol. 1983 Apr;33(2):409-13. doi: 10.1254/jjp.33.409.

Abstract

Methoxamine, isoprenaline, salbutamol and dobutamine were used to inhibit the spontaneous contraction of various rabbit small and large intestinal sections. From the concentration of the drugs that produced a similar magnitude of inhibition of the spontaneous contraction, the following deductions were made: The small intestine compared to the large intestine responded more to methoxamine, indicating a predominant presence of alpha receptors in the small intestine. The reverse is true for isoprenaline, indicating a predominant presence of beta receptors in the large intestine. Salbutamol exerted a much greater effect on the large intestine than on the small intestine, indicating that the beta receptors of the large intestine are mainly of the beta2 type. The reverse is true for dobutamine, suggesting that the beta receptors of the small intestine may be mainly of the beta1 type. The second deduction agreed with the findings of Nakahata and co-workers who reported similar, though qualitative, findings in the rat and rabbit intestine. The third and fourth deductions are interesting in that the facts complement the century old acupuncture classification of paired meridian which grouped the lung and large intestine as a pair and the heart and small intestine as another pair. The lung has beta2 and the heart beta1 receptors.

摘要

使用甲氧明、异丙肾上腺素、沙丁胺醇和多巴酚丁胺抑制兔不同小肠和大肠段的自发收缩。根据产生相似程度自发收缩抑制作用的药物浓度,得出以下推论:与大肠相比,小肠对甲氧明的反应更强,表明小肠中α受体占主导。而异丙肾上腺素则相反,表明大肠中β受体占主导。沙丁胺醇对大肠的作用比对小肠大得多,表明大肠的β受体主要是β2型。多巴酚丁胺则相反,表明小肠的β受体可能主要是β1型。第二个推论与中畑及其同事的研究结果一致,他们在大鼠和兔肠道中报告了类似的(尽管是定性的)结果。第三和第四个推论很有趣,因为这些事实补充了有着百年历史的经络配对针灸分类,该分类将肺和大肠归为一对,心和小肠归为另一对。肺有β2受体,心有β1受体。

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