Bowes M P, Swanson S, Zivin J A
Department of Neurosciences, School of Medicine, University of California, San Diego, La Jolla 92093-0624, USA.
J Cereb Blood Flow Metab. 1996 Sep;16(5):967-72. doi: 10.1097/00004647-199609000-00021.
Glutamate (Glu) neurotoxicity is an important element of a number of neurological disorders including central nervous system (CNS) ischemia. We evaluated the effects of the novel AMPA Glu antagonist LY293558 on functional neurological outcome in two rabbit stroke models. In the reversible spinal cord ischemia model, ischemia of the caudal lumbar spinal cord was produced by temporary occlusion of the abdominal aorta. LY293558 was administered 5 min after recirculation as a 16 mg/kg i.v. bolus followed by 2.2 mg/kg infused over 1 h. Control animals received saline. LY293558 significantly increased the duration of ischemia required to produce paraplegia, from 30.5 +/- 15.8 min (mean +/- SD) controls to 50.1 +/- 11.5 in treated animals (p < 0.01). In an irreversible model of cerebral ischemia, 50 microns plastic microspheres were injected into the carotid artery and lodged in the cerebral microvasculature. LY293558 did not significantly reduce neurological damage in this model. These data suggest that LY293558 may have therapeutic benefit following some types of ischemic injury.
谷氨酸(Glu)神经毒性是包括中枢神经系统(CNS)缺血在内的多种神经系统疾病的重要因素。我们评估了新型AMPA Glu拮抗剂LY293558对两种兔中风模型功能神经学转归的影响。在可逆性脊髓缺血模型中,通过暂时阻断腹主动脉产生尾侧腰段脊髓缺血。再灌注5分钟后静脉推注16mg/kg的LY293558,随后1小时内输注2.2mg/kg。对照动物接受生理盐水。LY293558显著增加了导致截瘫所需的缺血持续时间,从对照组的30.5±15.8分钟(平均值±标准差)增加到治疗组动物的50.1±11.5分钟(p<0.01)。在不可逆性脑缺血模型中,将50微米的塑料微球注入颈动脉并滞留在脑微血管中。在该模型中,LY293558并未显著减轻神经损伤。这些数据表明,LY293558可能对某些类型的缺血性损伤具有治疗益处。