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首页> 外文期刊>European Journal of Pharmacology: An International Journal >Does Cl(-)/HCO(3)(-) exchange play an important role in reperfusion arrhythmias in rats?
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Does Cl(-)/HCO(3)(-) exchange play an important role in reperfusion arrhythmias in rats?

机译:Cl(-)/ HCO(3)(-)交换在大鼠再灌注性心律不齐中起重要作用吗?

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摘要

The protective effects of Cl(-)/HCO(3)(-) exchange inhibitors, 4,4'-diisothiocyano-stilbene-2,2'-disulfonic acid (DIDS) and 4-acetamido-4'isothiocyanato-stilbene-2,2'-disulfonic acid (SITS), against reperfusion-induced arrhythmias were investigated in anesthetized rats. Rats were subjected to 5-min occlusion of the left coronary artery followed by 10-min reperfusion. All drugs were intravenously administered 5 min before the onset of occlusion. DIDS (75 mg/kg) reduced the incidence of ventricular fibrillation and mortality to 0%, whereas SITS (75 mg/kg) only decreased these parameters to 60%. DIDS simultaneously decreased the mean blood pressure and heart rate, and prolonged PQ and QRS intervals, whereas SITS produced a weaker effect on these parameters and no change in QRS interval. Mexiletine (5 mg/kg), which had been demonstrated to suppress the arrhythmias and reduce the heart rate and mean blood pressure in this model, was shown to prolong PQ and QRS intervals. Verapamil (0.5 mg/kg) or diltiazem (0.4 mg/kg) suppressed the arrhythmias, simultaneously decreasing the heart rate and mean blood pressure and prolonging PQ interval. The results indicate that the protective effect of DIDS on reperfusion arrhythmias in the anesthetized rats is unlikely to be attributed to the inhibitory action on Cl(-)/HCO(3)(-) exchange, but possibly mediated by its blocking effects on cardiac ion channels, such as Na(+) or Ca(2+) channels.
机译:Cl(-)/ HCO(3)(-)交换抑制剂,4,4'-diisothiocyano-stilbene-2,2'-disulfonic acid(DIDS)和4-acetamido-4'isothiocyanato-stilbene-2的保护作用在麻醉大鼠中研究了抗再灌注引起的心律失常的2,2'-二磺酸(SITS)。将大鼠的左冠状动脉阻塞5分钟,然后再灌注10分钟。在闭塞开始前5分钟静脉注射所有药物。 DIDS(75 mg / kg)将心室纤颤和死亡率的发生率降低至0%,而SITS(75 mg / kg)仅将这些参数降低至60%。 DIDS同时降低了平均血压和心率,并延长了PQ和QRS间隔,而SITS对这些参数的作用较小,QRS间隔不变。在该模型中,已证明美西律(5 mg / kg)可抑制心律不齐并降低心率和平均血压,但可延长PQ和QRS间隔。维拉帕米(0.5 mg / kg)或地尔硫卓(0.4 mg / kg)抑制心律不齐,同时降低心率和平均血压并延长PQ间隔。结果表明,DIDS对麻醉大鼠再灌注性心律失常的保护作用不太可能归因于对Cl(-)/ HCO(3)(-)交换的抑制作用,但可能是由其对心脏离子的阻断作用所介导的通道,例如Na(+)或Ca(2+)通道。

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