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甲硝唑诱导的心肌抑制:钙在体外作用的化学与药理学研究

Metronidazole-induced myocardial depression: chemical and pharmacological studies on the role of calcium in-vitro.

作者信息

Essien E E, Femi-Onadeko B, Ojewole J A

出版信息

J Pharm Pharmacol. 1985 Mar;37(3):213-6. doi: 10.1111/j.2042-7158.1985.tb05047.x.

Abstract

The interaction of metronidazole with calcium to form a water-soluble complex has been studied by titration with ethylenediaminetetraacetate (EDTA), direct current and pulse polarographic reduction steps of the nitro-group at pH 5 and 7, and by ultraviolet absorption. Stoichiometric calculations, X-ray powder diffraction pattern of the synthesized metronidazole-calcium complex, and molecular ion peak at m/z 381 in the mass spectrum of this product, showed that a 2:1 complex is formed. The interaction of metronidazole with calcium on myocardial contractile performance of guinea-pig electrically-driven isolated left atria in physiological solution was also examined. Metronidazole induced a sustained, concentration-dependent depression of the tension that was reversed by changing the bathing fluid to physiological solution, and/or by adding excess calcium ion. The drug-induced negative inotropic response was antagonized competitively by increasing calcium ion in the bath, whereas noradrenaline antagonized metronidazole-induced negative inotropic responses non-competitively. Addition of the metronidazole-calcium complex to the bath did not affect normal myocardial contractile performance. The results show that metronidazole produces a direct negative inotropic effect on isolated atrial muscles by interfering with Ca2+, and by preventing Ca2+ function in the events leading to contractile activity of atrial muscles.

摘要

已通过用乙二胺四乙酸(EDTA)滴定、在pH 5和7条件下硝基的直流和脉冲极谱还原步骤以及紫外吸收研究了甲硝唑与钙形成水溶性络合物的相互作用。化学计量计算、合成的甲硝唑 - 钙络合物的X射线粉末衍射图谱以及该产物质谱中m/z 381处的分子离子峰表明形成了2:1的络合物。还研究了甲硝唑与钙对生理溶液中豚鼠电驱动离体左心房心肌收缩性能的相互作用。甲硝唑引起张力的持续、浓度依赖性降低,通过将浴液换成生理溶液和/或添加过量钙离子可使其逆转。浴液中钙离子增加可竞争性拮抗药物诱导的负性肌力反应,而去甲肾上腺素则非竞争性拮抗甲硝唑诱导的负性肌力反应。向浴液中添加甲硝唑 - 钙络合物不影响正常心肌收缩性能。结果表明,甲硝唑通过干扰Ca2+并阻止Ca2+在导致心房肌收缩活动的事件中发挥作用,对离体心房肌产生直接的负性肌力作用。

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