Shaw P J
Department of Neurology, Royal Victoria Infirmary, Newcastle upon Tyne, UK.
Curr Opin Neurol Neurosurg. 1993 Jun;6(3):414-22.
Glutamate receptors continued to be the subject of intense investigation during 1992. It is clear that there is great structural and functional diversity within this receptor family, although the precise subunit structure of excitatory amino acid (EAA) receptors in specific neuronal groups within the human central nervous system remains to be determined. Molecular studies have shown the existence of five genes encoding N-methyl-D-aspartate receptor subunits that have specific anatomic profiles and differing functional properties. The chromosomal localization of several genes encoding EAA receptor subunits has been established and some of these represent candidate genes for clinical neurologic disorders. Further insights were gained into the functions of metabotropic receptors, and three distinct genes encoding glutamate transporters were cloned. The interaction between neurotrophic factors and EAA neurotransmitters is increasingly recognized. Excitotoxicity is considered to represent a final common pathway of neuronal injury in an ever-increasing range of neurologic disorders. The development of therapeutic agents has focused on methods for reducing excitotoxicity without interfering with EAA receptor activation.
1992年期间,谷氨酸受体仍是深入研究的对象。很明显,该受体家族存在巨大的结构和功能多样性,尽管人类中枢神经系统特定神经元群中兴奋性氨基酸(EAA)受体的确切亚基结构仍有待确定。分子研究表明,存在五个编码N-甲基-D-天冬氨酸受体亚基的基因,这些亚基具有特定的解剖学特征和不同的功能特性。已确定了几个编码EAA受体亚基的基因的染色体定位,其中一些是临床神经系统疾病的候选基因。对代谢型受体的功能有了进一步的认识,克隆了三个编码谷氨酸转运体的不同基因。神经营养因子与EAA神经递质之间的相互作用越来越受到认可。兴奋性毒性被认为是越来越多神经系统疾病中神经元损伤的最终共同途径。治疗药物的开发集中在减少兴奋性毒性而不干扰EAA受体激活的方法上。