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首页> 外文期刊>Brain research >Extended therapeutic time window after focal cerebral ischemia by non-competitive inhibition of AMPA receptors.
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Extended therapeutic time window after focal cerebral ischemia by non-competitive inhibition of AMPA receptors.

机译:通过非竞争性抑制AMPA受体延长局灶性脑缺血后的治疗时间范围。

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摘要

In acute stroke, the therapeutic time window is a critical factor which may have contributed to the failure of several phase III clinical trials with so-called neuroprotective agents. Since cerebral glutamate levels are elevated for many hours in progressing stroke, we investigated the novel AMPA glutamate receptor antagonist ZK 187638 in rodent models of stroke using up to 12 h delays in the start of therapy after permanent occlusion of the middle cerebral artery (MCA). In rats, ZK 187638 reduced total infarct volume by 43% and 33% when therapy was started immediately or with a delay of 6 h, respectively, but no effect was observed after a 12 h delay. Dose-dependent decreases of total infarct volume (up to 42%) were measured in mice given the first injection of ZK 187638 6 h after permanent MCA occlusion. In conclusion, the AMPA receptor antagonist ZK 187638 has a therapeutic time window of at least 6 h after permanent focal cerebral ischemia in rodents.
机译:在急性中风中,治疗时间窗是一个关键因素,可能会导致使用所谓的神经保护剂的几项III期临床试验失败。由于在进行性脑卒中后许多小时大脑谷氨酸水平都会升高,因此我们在啮齿动物模型中研究了新型AMPA谷氨酸受体拮抗剂ZK 187638,在大脑中动脉(MCA)永久性闭塞后开始治疗最多延迟了12小时。在大鼠中,当立即开始治疗或延迟6 h进行治疗时,ZK 187638分别将总梗死体积减少了43%和33%,但在延迟12 h后未观察到效果。在永久性MCA闭塞6小时后首次注射ZK 187638的小鼠中,测量了总梗塞体积的剂量依赖性减少(最高42%)。总之,AMPA受体拮抗剂ZK 187638在啮齿动物永久性局灶性脑缺血后的治疗时间窗至少为6小时。

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