Brain dopamine receptors in schizophrenia and tardive dyskinesia.

Psychopharmacology. Supplementum Pub Date : 1985-01-01
P Seeman
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Abstract

Brain dopamine receptors (type D2) mediate the psychomotor effects of dopamine. The D2 dopamine receptor can exist in either a high-affinity state for dopamine (nanomolar dissociation constant) or in a low-affinity state (micromolar dissociation constant). Both states of the receptor, however, have high affinity for neuroleptics (60 pM for spiperone). The postsynaptic receptor probably operates mainly in the D2 slow state. The presynaptic dopamine receptor, and also the dopamine receptors in the pituitary gland and the area postrema, probably function in the D2 high state. The density of brain D2 dopamine receptors is elevated in schizophrenia. The control densities were 10.5 pmol per g tissue. Half of the schizophrenic tissues (putamen, caudate nucleus, and nucleus accumbens) revealed densities of about 11.9 pmol per g, while the other half of the tissues revealed a density mode of 23.8 pmol per g. The bimodal distribution may support the concept of two types of schizophrenia. Future work must decide which group has more tardive dyskinesia.

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精神分裂症和迟发性运动障碍的脑多巴胺受体。
脑多巴胺受体(D2型)介导多巴胺的精神运动效应。D2多巴胺受体可以存在于多巴胺的高亲和力状态(纳摩尔解离常数)或低亲和力状态(微摩尔解离常数)。然而,受体的两种状态都对神经抑制剂有高亲和力(60 pM对spiperone)。突触后受体可能主要在D2慢状态下起作用。突触前多巴胺受体,以及脑垂体和脑后区域的多巴胺受体,可能在D2高状态下起作用。精神分裂症患者脑D2多巴胺受体密度升高。对照密度为10.5 pmol / g组织。一半的精神分裂症组织(壳核、尾状核和伏隔核)显示密度约为11.9 pmol / g,而另一半组织显示密度模式为23.8 pmol / g。这种双峰分布可能支持两种精神分裂症的概念。未来的工作必须确定哪一组有更多的迟发性运动障碍。
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Tardive dyskinesia: reversible and irreversible. Receptor-binding profiles of neuroleptics. Pathophysiological mechanisms underlying tardive dyskinesia. Chemical and structural changes in the brain in patients with movement disorder. Medical treatment of dystonia.
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