Moradi Somayeh, Nikoui Vahid, Imran Khan Muhammad, Amiri Shayan, Jazaeri Farahnaz, Bakhtiarian Azam
Department of Pharmacology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Razi Institute for Drug Research, Iran University of Medical Sciences, Tehran, Iran; Department of Pharmacology, Faculty of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Adv Pharmacol Sci. 2016;2016:9128018. doi: 10.1155/2016/9128018. Epub 2016 Feb 10.
Considering the cardioprotective and anti-inflammatory properties of clofibrate, the aim of the present experiment was to investigate the involvement of local and systemic inflammatory cytokines in possible antiarrhythmic effects of clofibrate in ouabain-induced arrhythmia in rats. Rats were orally treated with clofibrate (300 mg/kg), and ouabain (0.56 mg/kg) was administered to animals intraperitoneally. After induction of anesthesia, the atria were isolated and the onset of arrhythmia and asystole was recorded. The levels of inflammatory cytokines in atria were also measured. Clofibrate significantly postponed the onset of arrhythmia and asystole when compared to control group (P ≤ 0.05 and P ≤ 0.01, resp.). While ouabain significantly increased the atrial beating rate in control group (P ≤ 0.05), same treatment did not show similar effect in clofibrate-treated group (P > 0.05). Injection of ouabain significantly increased the atrial and systemic levels of all studied inflammatory cytokines (P ≤ 0.05). Pretreatment with clofibrate could attenuate the ouabain-induced elevation of IL-6 and TNF-α in atria (P ≤ 0.01 and P ≤ 0.05, resp.), as well as ouabain-induced increase in IL-6 in plasma (P ≤ 0.05). Based on our findings, clofibrate may possess antiarrhythmic properties through mitigating the local and systemic inflammatory factors including IL-6 and TNF-α.
鉴于氯贝丁酯的心脏保护和抗炎特性,本实验旨在研究局部和全身炎症细胞因子在氯贝丁酯对哇巴因诱导的大鼠心律失常可能的抗心律失常作用中的参与情况。大鼠口服氯贝丁酯(300mg/kg),并腹腔注射哇巴因(0.56mg/kg)。诱导麻醉后,分离心房并记录心律失常和心搏停止的发作情况。还测量了心房中炎症细胞因子的水平。与对照组相比,氯贝丁酯显著推迟了心律失常和心搏停止的发作(分别为P≤0.05和P≤0.01)。虽然哇巴因在对照组中显著增加了心房跳动率(P≤0.05),但相同处理在氯贝丁酯处理组中未显示出类似效果(P>0.05)。注射哇巴因显著增加了所有研究的炎症细胞因子的心房和全身水平(P≤0.05)。氯贝丁酯预处理可减轻哇巴因诱导的心房中IL-6和TNF-α升高(分别为P≤0.01和P≤0.05),以及哇巴因诱导的血浆中IL-6升高(P≤0.05)。基于我们的研究结果,氯贝丁酯可能通过减轻包括IL-6和TNF-α在内的局部和全身炎症因子而具有抗心律失常特性。