Aparicio-Legarza M I, Davis B, Hutson P H, Reynolds G P
Department of Biomedical Science, The University of Sheffield, UK.
Neurosci Lett. 1998 Jan 30;241(2-3):143-6. doi: 10.1016/s0304-3940(98)00017-2.
Saturable radioligand binding of [3H]L-689,560 to the glycine site of the N-methyl-D-aspartate (NMDA) glutamate receptor complex was employed to determine the density of this receptor in putamen, caudate and nucleus accumbens taken post mortem from schizophrenic patients and matched controls. Receptor density was found to be significantly increased in putamen of schizophrenics (P=0.012), although no significant change was found in the other two areas studied. Further experiments following 21 days administration of haloperidol to rats provided no evidence that the increase was related to prior drug treatment.
采用[3H]L-689,560与N-甲基-D-天冬氨酸(NMDA)谷氨酸受体复合物甘氨酸位点的饱和放射性配体结合法,来测定精神分裂症患者和匹配对照组死后壳核、尾状核和伏隔核中该受体的密度。结果发现,精神分裂症患者壳核中的受体密度显著增加(P = 0.012),不过在所研究的其他两个区域未发现显著变化。对大鼠给予氟哌啶醇21天后进行的进一步实验未提供证据表明这种增加与先前的药物治疗有关。