Henrich-Noack P, Hatton C D, Reymann K G
Department of Neurophysiology, Federal Institute for Neurobiology, Magdeburg, Germany.
Neuroreport. 1998 Apr 20;9(6):985-8. doi: 10.1097/00001756-199804200-00006.
(S)-4-Carboxy-3-hydroxy-phenylglycine [(S)-4C3HPG] is a potent competitive antagonist at the metabotropic glutamate receptor 1 subtype (mGlu1 receptor) and an agonist at mGlu2/3 receptor. We evaluated histologically the effect of this compound on transient global ischaemia in gerbils and observed pronounced neuroprotection in the CA1 layer of the hippocampus. When (S)-4C3HPG (1 microM) was administered intra-cerebroventricularly (i.c.v.) 20 min before clamping both common carotid arteries neuronal density was comparable with that in sham-operated animals. A single injection (1 microM) 65 min after ischaemia also significantly reduced neuronal damage. The results suggest that metabotropic glutamate receptors play a role in the deleterious cascade which leads to neuronal damage of pyramidal cells in the CA1 layer of the hippocampus after transient global ischaemia.
(S)-4-羧基-3-羟基苯甘氨酸[(S)-4C3HPG]是代谢型谷氨酸受体1亚型(mGlu1受体)的强效竞争性拮抗剂,也是mGlu2/3受体的激动剂。我们通过组织学方法评估了该化合物对沙鼠短暂性全脑缺血的影响,并在海马体CA1层观察到明显的神经保护作用。在夹闭双侧颈总动脉前20分钟经脑室内(i.c.v.)给予(S)-4C3HPG(1微摩尔)时,神经元密度与假手术动物相当。缺血65分钟后单次注射(1微摩尔)也显著减少了神经元损伤。结果表明,代谢型谷氨酸受体在导致短暂性全脑缺血后海马体CA1层锥体细胞神经元损伤的有害级联反应中起作用。