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首页> 外文期刊>Brain research >Cerebroprotective effects of TAK-937, a novel cannabinoid receptor agonist, in permanent and thrombotic focal cerebral ischemia in rats: Therapeutic time window, combination with t-PA and efficacy in aged rats
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Cerebroprotective effects of TAK-937, a novel cannabinoid receptor agonist, in permanent and thrombotic focal cerebral ischemia in rats: Therapeutic time window, combination with t-PA and efficacy in aged rats

机译:TAK-937,一种新型大麻素受体激动剂,对大鼠永久性和血栓性局灶性脑缺血的脑保护作用:治疗时间窗,t-PA联合治疗和对老年大鼠的疗效

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摘要

Some occluded arteries of acute ischemic stroke (AIS) patients are not recanalized, even if thrombolytic therapy is performed. Considering such clinical settings, we examined the potential cerebroprotective efficacy of TAK-937, a novel cannabinoid receptor agonist, in young adult and aged rats with a permanent middle cerebral artery occlusion (MCAO) model and conducted a combination study with TAK-937 and tissue type plasminogen activator (t-PA) in a rat thrombotic MCAO model. TAK-937 significantly reduced infarct volume when it was administered 3 and 5 h after permanent MCAO in young adult rats. A thrombotic MCAO was induced by photo-irradiation of the middle cerebral artery with Rose Bengal administration and a permanent MCAO was produced by thermoelectric coagulation of occluded arteries. TAK-937 (10, 30 and 100 μg/kg/h) was intravenously infused 1, 3, 5, or 8-24 h after MCAO. t-PA (3 or 10 mg/kg) was intravenously administered 1, 1.5 or 2 h after MCAO. Infarct volume was determined using a 2,3,5-triphenyltetrazolium chloride staining method 24 or 48 h after MCAO. The combined treatment of TAK-937 with t-PA significantly reduced the cerebral infarction compared with t-PA treatment alone in a rat thrombotic MCAO model. TAK-937 reduced infarct volume of aged rats as well, when it was administered 1 h after permanent MCAO. These results suggest that TAK-937 exerts protective effects regardless of age and has a wide therapeutic time window in permanent occlusion. Furthermore, combined treatment of TAK-937 with t-PA would provide more therapeutic efficacy compared to t-PA treatment alone.
机译:即使进行了溶栓治疗,某些急性缺血性卒中(AIS)患者的阻塞动脉也不会再通。考虑到这种临床情况,我们研究了新型大麻素受体激动剂TAK-937在具有永久性大脑中动脉闭塞(MCAO)模型的成年和成年大鼠中的潜在脑保护作用,并与TAK-937和组织进行了联合研究大鼠血栓性MCAO模型中的纤溶酶原激活剂(t-PA)类型。当在年轻成年大鼠中进行永久性MCAO后3和5小时给予TAK-937时,可显着减少梗死体积。玫瑰红给药后,通过大脑中动脉的光照射可诱发血栓性MCAO,而热热凝结闭塞的动脉可产生永久性MCAO。在MCAO后1、3、5或8-24小时静脉内注入TAK-937(10、30和100μg/ kg / h)。在MCAO后1、1.5或2小时静脉内施用t-PA(3或10 mg / kg)。在MCAO后24或48小时,使用2,3,5-三苯基四唑氯化物染色法测定梗塞体积。在大鼠血栓性MCAO模型中,与单独使用t-PA治疗相比,将TAK-937与t-PA联合治疗可显着减少脑梗塞。当永久性MCAO给药1小时后,TAK-937也减少了老年大鼠的梗塞体积。这些结果表明,TAK-937不论年龄大小都发挥保护作用,并且在永久性闭塞方面具有宽广的治疗时间范围。此外,与单独的t-PA治疗相比,TAK-937与t-PA的联合治疗将提供更多的治疗功效。

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