Briyal S, Gulati A, Gupta Y K
Neuropharmacology Laboratory, Department of Pharmacology, All India Institute of Medical Sciences, New Delhi, India.
Methods Find Exp Clin Pharmacol. 2007 May;29(4):257-63. doi: 10.1358/mf.2007.29.4.1106409.
The present study was carried out to investigate the effect of the combination of an endothelin antagonist TAK-044 and an antiinflammatory agent aspirin in middle cerebral artery (MCA) occlusion model of acute ischemic stroke in rats. Male Wistar rats were pretreated with TAK-044 (5 mg/kg, i.p.) and aspirin (50 mg/kg, i.p.) for 7 days individually and in combination in different groups, and were thereafter subjected to focal ischemia for 2 h by occlusion of MCA using intraluminal thread. Twenty-four hours later, the rats were subjected to motor performance tests and killed subsequently for estimation of markers of oxidative stress malondialdehyde (MDA), reduced glutathione (GSH) and superoxide dismutase (SOD). The control group received the vehicle and the same protocol was followed. In vehicle-treated MCA occluded rats, significant (p < 0.01) motor impairment, with elevated levels of MDA (600.8 +/- 14.4 nmol/g tissue) and decreased levels of GSH (61.1 +/- 3.1 microg/g tissue) and SOD (8.5 +/- 0.5 U/mg protein,) was observed. Pretreatment with TAK-044 and aspirin for 7 days significantly improved motor function and attenuated the raised levels of MDA (475 +/- 14 and 538 +/- 17.3 nmol/g tissue, respectively) and the decrease in GSH (101 +/- 5 and 100 +/- 4.5 microg/g tissue, respectively) and SOD (12.1 +/- 0.5 and 10.5 +/- 0.6 U/mg protein, respectively), as compared to vehicle-treated MCA occluded rats. Combination of both the agents did not show a significant difference as compared to the individual drugs alone. The present study demonstrates that, although protection was observed with both the drugs (TAK-044 and aspirin), there was no enhanced effect when both agents were given in combination.
本研究旨在探讨内皮素拮抗剂TAK - 044与抗炎药物阿司匹林联合应用对大鼠大脑中动脉(MCA)闭塞急性缺血性卒中模型的影响。将雄性Wistar大鼠分为不同组,分别单独及联合给予TAK - 044(5 mg/kg,腹腔注射)和阿司匹林(50 mg/kg,腹腔注射)预处理7天,之后通过腔内丝线闭塞MCA使其局灶性缺血2小时。24小时后,对大鼠进行运动功能测试,随后处死以评估氧化应激标志物丙二醛(MDA)、还原型谷胱甘肽(GSH)和超氧化物歧化酶(SOD)。对照组给予溶媒并遵循相同方案。在给予溶媒处理的MCA闭塞大鼠中,观察到显著的(p < 0.01)运动功能障碍,MDA水平升高(600.8 ± 14.4 nmol/g组织),GSH水平降低(61.1 ± 3.1 μg/g组织),SOD水平降低(8.5 ± 0.5 U/mg蛋白)。与给予溶媒处理的MCA闭塞大鼠相比,TAK - 044和阿司匹林预处理7天显著改善了运动功能,并减轻了MDA水平的升高(分别为475 ± 14和538 ± 17.3 nmol/g组织)以及GSH水平的降低(分别为101 ± 5和100 ± 4.5 μg/g组织)和SOD水平的降低(分别为12.1 ± 0.5和10.5 ± 0.6 U/mg蛋白)。与单独使用两种药物相比,两种药物联合使用未显示出显著差异。本研究表明,尽管两种药物(TAK - 044和阿司匹林)均观察到了保护作用,但联合使用时并未产生增强效应。