Simon R P, Swan J H, Griffiths T, Meldrum B S
Science. 1984 Nov 16;226(4676):850-2. doi: 10.1126/science.6093256.
In rats ischemia of the forebrain induced by a 30-minute occlusion of the carotid artery, followed by 120 minutes of arterial reperfusion, produced ischemic lesions of selectively vulnerable pyramidal cells in both hippocampi. Focal microinfusion into the dorsal hippocampus of 2-amino-7-phosphonoheptanoic acid, an antagonist of excitation at the N-methyl-D-aspartate-preferring receptor, before ischemia was induced protected against the development of ischemic damage. It is proposed that excitatory neurotransmission plays an important role in selective neuronal loss due to cerebral ischemia.
在大鼠中,通过30分钟的颈动脉闭塞诱导前脑缺血,随后进行120分钟的动脉再灌注,导致双侧海马中选择性易损锥体细胞出现缺血性损伤。在诱导缺血前,向背侧海马局部微量注入N-甲基-D-天冬氨酸优先受体兴奋拮抗剂2-氨基-7-磷酸庚酸,可预防缺血性损伤的发展。有人提出,兴奋性神经传递在脑缺血导致的选择性神经元丢失中起重要作用。