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前列腺素对豚鼠离体胆囊中儿茶酚胺诱导的收缩的作用。

Contribution of prostaglandin to the contraction induced by catecholamines in the isolated gallbladder of the guinea-pig.

作者信息

Yamamoto F

出版信息

Gastroenterol Jpn. 1980;15(5):433-8. doi: 10.1007/BF02773904.

Abstract

Possible contribution of prostaglandins to the mechanical response produced by catecholamines was investigated in the isolated strips of the guinea-pig gallbladder. The contraction by catecholamine was blocked by an alpha-blocker, phentolamine (10(-6)M and relaxation was blocked by a beta-blocker, propranolol (10(-6)M. The rhythmic spontaneous motility and intrinsic tone were markedly inhibited by a prostaglandin synthesis inhibitor, indomethacin (10(-7)M. Furthermore, exogenous prostaglandins F2 alpha, E1 and E2 produced potent stimulant actions on gallbladder and the order of potency was found to be E2 > E1 > F2 alpha. The contractile response of catecholamines was abolished almost completely by indomethacin (10(-7)M. Even after the muscle tone was elevated by exogenous prostaglandin after treatment with indomethacin, catecholamine produced no contractile response, although it still relaxed the preparation through activation of beta-receptor. Based on these results, it was suggested that endogenous prostaglandins appear to be contributed to the alpha-action of catecholamines in the isolated guinea-pig gallbladder.

摘要

在豚鼠胆囊离体条带上研究了前列腺素对儿茶酚胺产生的机械反应的可能作用。儿茶酚胺引起的收缩被α受体阻滞剂酚妥拉明(10⁻⁶M)阻断,舒张被β受体阻滞剂普萘洛尔(10⁻⁶M)阻断。前列腺素合成抑制剂吲哚美辛(10⁻⁷M)显著抑制节律性自发运动和内在张力。此外,外源性前列腺素F2α、E1和E2对胆囊产生强效刺激作用,发现其效力顺序为E2>E1>F2α。吲哚美辛(10⁻⁷M)几乎完全消除了儿茶酚胺的收缩反应。即使在用吲哚美辛处理后通过外源性前列腺素提高肌张力,儿茶酚胺也不产生收缩反应,尽管它仍通过激活β受体使标本舒张。基于这些结果,提示内源性前列腺素似乎参与了豚鼠离体胆囊中儿茶酚胺的α作用。

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