Lam A G, Soriano M A, Monn J A, Schoepp D D, Lodge D, McCulloch J
Wellcome Surgical Institute and Hugh Fraser Neuroscience Laboratories, University of Glasgow, UK. 9509428/@udcf.gla.ac.uk
Neurosci Lett. 1998 Sep 25;254(2):121-3. doi: 10.1016/s0304-3940(98)00651-x.
The neuroprotective effects of a systemically active, potent, group II selective metabotropic glutamate receptor agonist, LY354740, was assessed in the middle cerebral artery occlusion model of focal ischaemia in rats. LY354740 (0.3, 3.0 or 30.0 mg/kg) was administered subcutaneously (s.c.) 30 min prior to and 3 hours after the induction of ischaemia. Twenty four hours after the ischaemic insult, the brains were processed for the evaluation of infarct volumes. No significant reduction in infarct volumes were observed in treated animals at any of the doses investigated. These data provide no support for the view that group II metabotropic glutamate receptors have a major influence on ischaemic damage in this model.
在大鼠局灶性缺血的大脑中动脉闭塞模型中,评估了一种具有全身活性、强效的II组选择性代谢型谷氨酸受体激动剂LY354740的神经保护作用。在缺血诱导前30分钟和缺血诱导后3小时,皮下注射(s.c.)LY354740(0.3、3.0或30.0mg/kg)。缺血损伤24小时后,对大脑进行处理以评估梗死体积。在所研究的任何剂量下,未观察到治疗动物的梗死体积有显著减少。这些数据不支持II组代谢型谷氨酸受体对该模型中的缺血性损伤有重大影响的观点。