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藜芦定对大鼠心房的正性肌力作用:类前列腺素可能参与其中。

Positive inotropic action of veratridine in rat atria: possible involvement of prostanoids.

作者信息

Morikawa M, Satake N, Shibata S, Shibata T

机构信息

Department of Pharmacology, Tokyo College of Pharmacy, Japan.

出版信息

Pharmacology. 1991;42(2):61-7. doi: 10.1159/000138774.

Abstract

Veratridine caused a positive inotropic action in the electrically driven left atria of rats. Quinacrine (a phospholipase A2 inhibitor), indomethacin (a cyclooxygenase inhibitor) and aspirin (a cyclooxygenase inhibitor), but not nordihydroguaiaretic acid (a lipoxygenase inhibitor), inhibited the response to veratridine. Verapamil and nifedipine also inhibited the response to veratridine. The positive inotropic effect of arachidonic acid was abolished by aspirin and indomethacin. However, the positive inotropic effect of PGF2 alpha was not affected by indomethacin, quinacrine or aspirin. PGE2, but not STA2 and PGI2, also caused the positive inotropic effect. However, the negative inotropic effect was observed in the presence of PGE1 and PGD2. Veratridine shifted the concentration-response curve of Ca2+ to the left in a Ca(2+)-free medium. Indomethacin only inhibited the veratridine-induced potentiation of Ca2+ responses. Veratridine increased the level of PGF2 alpha in the left atria and this action was completely inhibited by indomethacin, aspirin and quinacrine. Veratridine also increased the level of PGE2. These results imply that the positive inotropic action of veratridine is partly due to stimulation of the release of arachidonic acid leading to the increase in prostaglandins in rat atria.

摘要

藜芦碱可使大鼠电驱动左心房产生正性肌力作用。奎纳克林(一种磷脂酶A2抑制剂)、吲哚美辛(一种环氧化酶抑制剂)和阿司匹林(一种环氧化酶抑制剂)可抑制对藜芦碱的反应,而去甲二氢愈创木酸(一种脂氧合酶抑制剂)则不能。维拉帕米和硝苯地平也可抑制对藜芦碱的反应。花生四烯酸的正性肌力作用可被阿司匹林和吲哚美辛消除。然而,前列腺素F2α的正性肌力作用不受吲哚美辛、奎纳克林或阿司匹林的影响。前列腺素E2也可产生正性肌力作用,而前列腺素STA2和前列环素则不能。然而,在前列腺素E1和前列腺素D2存在的情况下可观察到负性肌力作用。在无钙培养基中,藜芦碱使钙离子浓度-反应曲线向左移动。吲哚美辛仅抑制藜芦碱诱导的钙离子反应增强。藜芦碱可使左心房中前列腺素F2α水平升高,这一作用可被吲哚美辛、阿司匹林和奎纳克林完全抑制。藜芦碱还可使前列腺素E2水平升高。这些结果表明,藜芦碱的正性肌力作用部分归因于刺激花生四烯酸释放,导致大鼠心房中前列腺素增加。

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