Park So Youn, Lee Jeong Hyun, Kim Chi Dae, Rhim Byung Yong, Hong Ki Whan, Lee Won Suk
Department of Pharmacology, College of Medicine, Pusan National University, Busan 602-739, Republic of Korea.
Brain Res. 2007 Jul 9;1157:112-20. doi: 10.1016/j.brainres.2007.04.051. Epub 2007 Apr 25.
In the present study, we assessed the beneficial synergistic effects of concurrent treatment with low doses of cilostazol and probucol against focal cerebral ischemic infarct in rats. The ischemic infarct induced by 2-h occlusion of middle cerebral artery (MCA) and 22-h reperfusion was significantly reduced in rat brain that received cilostazol (20 mg/kg) and probucol (30 mg/kg) twice together with prominent improvement of neurological function compared to the effect of cilostazol or probucol monotherapy. Increased myeloperoxidase activity, a marker of neutrophil infiltration, observed in the penumbral zone of vehicle-treated brain was more significantly reduced by cilostazol plus probucol in combination. Increased superoxide-, nitrotyrosine (a marker of peroxynitrite)-, poly(ADP-ribose) [a marker for poly(ADP-ribose) polymerase activity]-, and cleaved caspase-3-positive cells (a proapoptotic marker) in the vehicle sample were significantly attenuated by the combination therapy, while individual treatment with low dose of cilostazol or probucol showed a marginal effect. Taken together, it is suggested that the neuroprotective potentials of combination therapy with low doses of cilostazol plus probucol may provide beneficial therapeutic intervention in reducing the focal cerebral ischemic infarct in rats.
在本研究中,我们评估了低剂量西洛他唑和普罗布考联合治疗对大鼠局灶性脑缺血梗死的有益协同作用。与西洛他唑或普罗布考单一疗法相比,在接受西洛他唑(20毫克/千克)和普罗布考(30毫克/千克)联合给药两次的大鼠脑中,大脑中动脉(MCA)闭塞2小时并再灌注22小时所诱导的缺血性梗死显著减少,神经功能也有显著改善。在给予赋形剂处理的大脑半暗带中观察到的髓过氧化物酶活性增加(中性粒细胞浸润的标志物),在西洛他唑加普罗布考联合治疗下更显著降低。联合治疗显著减弱了赋形剂样本中超氧化物、硝基酪氨酸(过氧亚硝酸盐的标志物)、聚(ADP - 核糖)[聚(ADP - 核糖)聚合酶活性的标志物]以及裂解的半胱天冬酶 - 3阳性细胞(促凋亡标志物)的增加,而低剂量西洛他唑或普罗布考单独治疗仅显示出微弱的效果。综上所述,低剂量西洛他唑加普罗布考联合治疗的神经保护潜力可能为减少大鼠局灶性脑缺血梗死提供有益的治疗干预。