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脂氧合酶抑制剂对离体灌流豚鼠心脏中地高辛诱导的心律失常的影响。

Effects of a lipoxygenase inhibitor on digoxin-induced cardiac arrhythmias in the isolated perfused guinea-pig heart.

作者信息

Gök S, Ulker S, Hüseyinov A, Evinç A

机构信息

Department of Pharmacology, School of Medicine, Celal Bayar University, Manisa, Turkey.

出版信息

Gen Pharmacol. 1997 Nov;29(5):789-92. doi: 10.1016/s0306-3623(97)00018-9.

Abstract
  1. The effects of a lipoxygenase inhibitor, BW A4C, on digoxin-induced arrhythmias and cardiac dynamics (contractile force, perfusion pressure, heart rate) were investigated in Langendorff-perfused isolated guinea-pig hearts. In the control group, arrhythmias were induced by 25 micrograms/ml digoxin at a perfusion rate of 0.5 ml/min. In the treated groups, BW A4C (1 and 0.3 microM) perfused continuously from 15 min prior to digoxin until cardiac arrest occurred. Digoxin exposure (microgram/g wet weight of heart) for the occurrence of arrhythmias and cardiac arrest were the parameters evaluated to assess cardiotoxicity. 2. Digoxin caused a marked increase in leukotriene B4 release in the coronary effluent, and was collected during tachyarrhythmias. BW A4C markedly inhibited the digoxin-induced elevation of LTB4. 3. BW A4C (1 and 0.3 microM) did not prevent the onset of ventricular fibrillation and ventricular tachycardia despite a slight delay in the occurrence of ventricular fibrillation and cardiac arrest at the 0.3 microM concentration. 4. Contractile force increased significantly after digoxin infusion which was concomitant with the time of onset of arrhythmias. In the presence of BW A4C, the contractile force increased, but not significantly. Perfusion pressure increased initially after digoxin infusion in the absence and the presence of BW A4C, but not significantly. 5. These findings show that the lipoxygenase inhibitor lacked any protective action on digoxin-induced arrhythmias despite its effective suppression of digoxin-induced elevation of LTB4 in coronary effluent.
摘要
  1. 在Langendorff灌流的离体豚鼠心脏中,研究了脂氧合酶抑制剂BW A4C对地高辛诱发的心律失常及心脏动力学(收缩力、灌注压、心率)的影响。对照组中,以0.5毫升/分钟的灌注速率用25微克/毫升地高辛诱发心律失常。在治疗组中,从地高辛给药前15分钟开始持续灌注BW A4C(1和0.3微摩尔),直至心脏停搏。评估心律失常和心脏停搏发生时地高辛的暴露量(微克/克心脏湿重),以此作为评估心脏毒性的参数。2. 地高辛导致冠状动脉流出液中白三烯B4释放显著增加,且在快速性心律失常期间收集流出液。BW A4C显著抑制地高辛诱导的LTB4升高。3. BW A4C(1和0.3微摩尔)并未预防室颤和室性心动过速的发生,尽管在0.3微摩尔浓度时室颤和心脏停搏的发生稍有延迟。4. 地高辛输注后收缩力显著增加,这与心律失常的发作时间一致。在BW A4C存在的情况下,收缩力也增加,但不显著。在有无BW A4C的情况下,地高辛输注后灌注压最初均升高,但不显著。5. 这些研究结果表明,尽管脂氧合酶抑制剂能有效抑制地高辛诱导的冠状动脉流出液中LTB4升高,但对地高辛诱发的心律失常没有任何保护作用。

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