Johnson M, Perry E K, Ince P G, Shaw P J, Perry R H
MRC Neurochemical Pathology Unit, Newcastle General Hospital, Newcastle upon Tyne, UK.
Brain Res. 1993 Jul 2;615(2):259-66. doi: 10.1016/0006-8993(93)90036-m.
The autoradiographic distribution of N-methyl-D-aspartate (NMDA) and D,L-a-amino-3-hydroxyl-5-methyl-4-isoxazoleproprionic acid/quisqualate (AMPA/QUIS) receptors was determined in cerebellum obtained at autopsy from 37 human individuals, aged from 24 weeks gestation to 95 years. [3H]MK801 was used to label the NMDA receptor and [3H]CNQX to label the AMPA/QUIS receptor. AMPA/QUIS receptors were concentrated in the cerebellar molecular layer, and NMDA receptors in the granular layer. Significant (3- to 4-fold) increases in binding were seen for both ligands from the fetal to neonatal periods in the molecular layer (CNQX) and in both molecular and granular layers (MK801). MK801 binding in the molecular layer continued to increase with age up to the tenth decade and together with binding in the granular layer, increased 2-fold between 10-40 years. The Purkinje cell layer was negative for MK801 binding until the 6-7th decade when it became positive. [3H]CNQX binding in the molecular layer increased significantly with age between the fetal period and the tenth decade, whereas in the granular layer binding increased from neonate to 40 years, but then decreased significantly from 60 years to the tenth decade. Lamination of the molecular and granular layers was absent during the fetal period and appeared with both ligands during the neonatal period. These marked differences in age-related expression of ligand binding sites in the granular layer during development and aging are of potential significance in relation both to selective vulnerability to ischemia, and synaptic plasticity and remodelling related to neuronal loss in senescence.
在取自37名年龄从妊娠24周至95岁个体尸检的小脑中,测定了N-甲基-D-天冬氨酸(NMDA)和D,L-α-氨基-3-羟基-5-甲基-4-异恶唑丙酸/quisqualate(AMPA/QUIS)受体的放射自显影分布。[3H]MK801用于标记NMDA受体,[3H]CNQX用于标记AMPA/QUIS受体。AMPA/QUIS受体集中在小脑分子层,而NMDA受体集中在颗粒层。在分子层(CNQX)以及分子层和颗粒层(MK801)中,从胎儿期到新生儿期,两种配体的结合均显著增加(3至4倍)。分子层中MK801的结合随年龄增长持续增加,直至第十个十年,并且与颗粒层中的结合一起,在10至40岁之间增加了2倍。直到第六至第七个十年浦肯野细胞层对MK801结合呈阴性,之后变为阳性。分子层中[3H]CNQX的结合在胎儿期到第十个十年之间随年龄显著增加,而在颗粒层中,结合从新生儿期到40岁增加,但随后从60岁到第十个十年显著下降。在胎儿期分子层和颗粒层不存在分层现象,在新生儿期两种配体均出现分层。在发育和衰老过程中颗粒层中配体结合位点与年龄相关的表达存在这些显著差异,对于与缺血选择性易损性以及与衰老中神经元丢失相关的突触可塑性和重塑均具有潜在意义。