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首页> 外文期刊>Japanese Journal of Pharmacology >COMPARISON OF ACTIONS OF PAPAVERINE, ASPAMINOL AND ISOPRENALINE ON ISOLATED RAT UTERUS
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COMPARISON OF ACTIONS OF PAPAVERINE, ASPAMINOL AND ISOPRENALINE ON ISOLATED RAT UTERUS

机译:罂粟碱,氨纶和异戊啉对离体大鼠子宫的作用比较

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References(19) Cited-By(15) Inhibitory responses of the isolated rat uterus to papaverine, Aspaminol and isoprenaline were potentiated by aminophylline that inhibits phosphodiesterase. The inhibitory responses to papaverine and isoprenaline were decreased by imidazole that stimulates phosphodicsterase activity, while the inhibitory response to Aspaminol was little influenced by imidazole. Papavcrine strongly inhibited phosphodiesterase from the rat uterus, but Aspaminol did not influence phosphodiesterase activity. These results indicate that papaverine and isoprenaline are mediated through an increase of the intracellular level of cyclic AMP and also indicate that the inhibitory response of the rat uterus to Aspaminol is not concerned with the amount of intracellular cyclic AMP increased by inhibiting phosphodiesterase. Further, the results support the theory that there are two mechanisms for the so-called papaverine-like antispasmodics.
机译:参考文献(19)被引用的By(15)通过抑制磷酸二酯酶的氨茶碱增强了离体大鼠子宫对罂粟碱,天冬酰胺和异丙肾上腺素的抑制反应。咪唑刺激磷酸二酯酶的活性降低了对罂粟碱和异丙肾上腺素的抑制反应,而咪唑对Aspaminol的抑制反应几乎没有影响。帕帕vcrine强烈抑制大鼠子宫中的磷酸二酯酶,但Aspaminol不会影响磷酸二酯酶的活性。这些结果表明罂粟碱和异丙肾上腺素是通过细胞内环状AMP水平的增加来介导的,并且还表明大鼠子宫对Aspaminol的抑制反应与通过抑制磷酸二酯酶增加的细胞内环状AMP的量无关。此外,结果支持了所谓的罂粟碱样解痉药有两种机制的理论。

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