精神分裂症患者和对照组内嗅皮层神经紧张素受体的放射自显像特征。

S S Wolf, T M Hyde, R C Saunders, M M Herman, D R Weinberger, J E Kleinman
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引用次数: 26

摘要

神经紧张素是一种内源性肽,被认为是一种神经递质,它与多巴胺能神经元有广泛的相互作用,并表现出一些类似于抗精神病药的作用。此外,神经紧张素受体在内嗅皮层的特定层中丰富,而在精神分裂症中,细胞结构异常已被报道。因此,我们使用受体放射自显影检查了5名对照患者和6名精神分裂症患者的死后标本的内嗅皮层,以观察神经紧张素受体的数量和分布的变化。特异性的125I-神经紧张素结合集中在第II层细胞簇中,精神分裂症组的结合减少了40% (p < 0.05)。在两个队列中,在深V/VI层均观察到中度结合,而在海马层的结合可忽略不计。与对照组相比,精神分裂症患者内嗅皮质其他层的神经紧张素结合量无统计学差异。典型的层流结合模式在队列之间没有差异。精神分裂症患者神经紧张素结合的减少与越来越多的关于精神分裂症患者内侧颞叶结构异常的报道是一致的,尤其是内鼻皮层。需要进一步的研究来检验内嗅皮层的神经解剖学和神经化学病理学证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Autoradiographic characterization of neurotensin receptors in the entorhinal cortex of schizophrenic patients and control subjects.

Neurotensin, an endogenous peptide and putative neurotransmitter, exhibits a wide range of interactions with dopaminergic neurons and displays some actions akin to neuroleptics. Moreover, neurotensin receptors are abundant in specific layers of the entorhinal cortex where cytoarchitectural abnormalities have been reported in schizophrenia. We therefore examined the entorhinal cortex from postmortem specimens of five control patients and six schizophrenic patients for alterations in neurotensin receptor quantitation and distribution using receptor autoradiography. Specific 125I- neurotensin binding was concentrated in layer II cell clusters, with a 40% reduction in binding in the schizophrenic group (p < 0.05). Moderate binding was observed in both cohorts in deep layers V/VI, with negligible binding in the hippocampus. There was no statistical difference in quantitative neurotensin binding in other lamina of the entorhinal cortex of schizophrenics compared with controls. The characteristic laminar pattern of binding did not differ between cohorts. The reduction in neurotensin binding in schizophrenics is consistent with an increasing number of reports of structural abnormalities in the medial temporal lobe of schizophrenics in general and the entorhinal cortex in particular. Further studies are required to examine the evidence for neuroanatomic and neurochemical pathology in the entorhinal cortex.

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