Dean B, Pavey G, Scarr E, Goeringer K, Copolov D L
The Rebecca L. Cooper Research Laboratory, The Mental Health Research Institute of Victoria, Parkville, Victoria 3052, Australia.
Life Sci. 2004 May 7;74(25):3115-31. doi: 10.1016/j.lfs.2003.11.004.
In situ radioligand binding with autoradiography and anti-human dopamine D(2) receptor antibodies with Western blots have been used to measure the density of dopamine D(2)-like receptors in the caudate-putamen and pituitary from schizophrenic subjects who did or did not have residual antipsychotic drugs in their tissue at death. There was a significant decrease in the Ki for haloperidol displaceable [(125)I]iodosulpride binding in the pituitary (p < 0.01) and caudate-putamen (p < 0.05) from subjects with schizophrenia with residual drugs in their tissue. There was a significant decrease in the density of [(125)I]iodosulpride in the pituitary (p < 0.001) and a strong trend to a decrease in binding in the caudate-putamen (p = 0.055) from subjects with schizophrenia. By contrast, [(3)H]spiperone binding was decreased in the caudate-putamen (p < 0.05) with a trend to decreased binding in the pituitary (p = 0.07) from subjects with schizophrenia. There was no difference in the density of dopamine D(2) receptors in the caudate-putamen from subjects with schizophrenia (p = 0.31). All the findings on receptor densities were independent of drug status. [(125)I]iodosulpride binds to the dopamine D(2&3) receptors. We have shown that there is no change in the dopamine D(2) receptor in the caudate-putamen from subjects with schizophrenia and therefore, these data would be consistent with there being a decrease in the dopamine D(3) in the caudate-putamen from subjects with schizophrenia. Since dopamine D(3) receptors are absent or present at low concentrations in the pituitary, our data would suggest the dopamine D(2) receptor is decreased in that tissue from schizophrenic subjects.
采用放射自显影原位放射配体结合法以及蛋白质免疫印迹法检测抗人多巴胺D(2)受体抗体,以测量精神分裂症患者尾状核-壳核和垂体中多巴胺D(2)样受体的密度,这些患者在死亡时组织中有无残留抗精神病药物。在组织中存在残留药物的精神分裂症患者的垂体(p < 0.01)和尾状核-壳核(p < 0.05)中,氟哌啶醇可置换的[(125)I]碘舒必利结合的Ki值显著降低。精神分裂症患者垂体中[(125)I]碘舒必利的密度显著降低(p < 0.001),尾状核-壳核中的结合有强烈的降低趋势(p = 0.055)。相比之下,精神分裂症患者尾状核-壳核中[(3)H]螺哌隆结合降低(p < 0.05),垂体中的结合有降低趋势(p = 0.07)。精神分裂症患者尾状核-壳核中多巴胺D(2)受体的密度没有差异(p = 0.31)。所有关于受体密度的发现均与药物状态无关。[(125)I]碘舒必利与多巴胺D(2&3)受体结合。我们已经表明,精神分裂症患者尾状核-壳核中的多巴胺D(2)受体没有变化,因此,这些数据与精神分裂症患者尾状核-壳核中多巴胺D(3)降低一致。由于垂体中不存在多巴胺D(3)受体或其浓度较低,我们的数据表明精神分裂症患者该组织中的多巴胺D(2)受体减少。