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七叶亭(6,7 - 二羟基香豆素)对豚鼠离体气管链的作用。

Effects of esculetin (6,7-dihydroxycoumarin) on guinea-pig tracheal chains in vitro.

作者信息

Ragazzi E, Froldi G, Fassina G

机构信息

Department of Pharmacology, University of Padova, Italy.

出版信息

Pharmacol Res. 1989 Mar-Apr;21(2):183-92. doi: 10.1016/1043-6618(89)90237-5.

Abstract

Esculetin (6,7-dihydroxycoumarin) was tested in isolated guinea-pig tracheal chains from normal and ovalbumin-sensitized animals. The drug showed a concentration-dependent relaxant effect, with an EC50 of 60 microM. Pretreatment with esculetin (30-60 microM) was not able to reduce the contractile response induced by either carbachol (0.1 microM), histamine (10 microM), BaCl2 (10 mM) or K+ (80 mM). Esculetin increased the contraction evoked by PGF2 alpha and by histamine, but reduced A23187-induced contraction. Mepacrine (10 microM), a phospholipase A2 inhibitor, reduced the relaxant effect of the lower esculetin concentrations (3-60 microM). Indomethacin (0.1 microM) increased the relaxation induced by esculetin (3-10 microM). In tracheal chains from ovalbumin-sensitized guinea-pigs, esculetin (60 microM) significantly reduced the duration of the recovery phase after antigen challenge contraction. In conclusion, in our in vitro conditions, this natural coumarin derivative seems to act by interfering with the arachidonic acid cascade.

摘要

七叶亭(6,7 - 二羟基香豆素)在来自正常和卵清蛋白致敏动物的豚鼠离体气管链中进行了测试。该药物呈现出浓度依赖性的舒张作用,半数有效浓度(EC50)为60微摩尔。用七叶亭(30 - 60微摩尔)预处理不能降低由卡巴胆碱(0.1微摩尔)、组胺(10微摩尔)、氯化钡(10毫摩尔)或钾离子(80毫摩尔)诱导的收缩反应。七叶亭增加了由前列腺素F2α和组胺引起的收缩,但降低了由A23187诱导的收缩。磷脂酶A2抑制剂米帕林(10微摩尔)降低了较低浓度七叶亭(3 - 60微摩尔)的舒张作用。吲哚美辛(0.1微摩尔)增强了七叶亭(3 - 10微摩尔)诱导的舒张。在来自卵清蛋白致敏豚鼠的气管链中,七叶亭(60微摩尔)显著缩短了抗原激发收缩后恢复阶段的持续时间。总之,在我们的体外实验条件下,这种天然香豆素衍生物似乎通过干扰花生四烯酸级联反应起作用。

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