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慢性精神分裂症中ATP结合盒转运蛋白ABCB1脑表达的形态计量学分析:缰核的局限性缺陷

Morphometric analysis of the cerebral expression of ATP-binding cassette transporter protein ABCB1 in chronic schizophrenia: Circumscribed deficits in the habenula.

作者信息

Bernstein Hans-Gert, Hildebrandt Jens, Dobrowolny Henrik, Steiner Johann, Bogerts Bernhard, Pahnke Jens

机构信息

Department of Psychiatry and Psychotherapy, University of Magdeburg, Germany.

Department of Psychiatry and Psychotherapy, University of Magdeburg, Germany.

出版信息

Schizophr Res. 2016 Nov;177(1-3):52-58. doi: 10.1016/j.schres.2016.02.036. Epub 2016 Mar 3.

Abstract

There is increasing evidence that microvascular abnormalities and malfunction of the blood-brain barrier (BBB) significantly contribute to schizophrenia pathophysiology. The ATP-binding cassette transporter ABCB1 is an important molecular component of the intact BBB, which has been implicated in a number of neurodegenerative and psychiatric disorders, including schizophrenia. However, the regional and cellular expression of ABCB1 in schizophrenia is yet unexplored. Therefore, we studied ABCB1 protein expression immunohistochemically in twelve human post-mortem brain regions known to play a role in schizophrenia, in 13 patients with schizophrenia and nine controls. In ten out of twelve brain regions under study, no significant differences were found with regard to the numerical density of ABCB1-expressing capillaries between all patients with schizophrenia and control cases. The left and right habenular complex, however, showed significantly reduced capillary densities in schizophrenia patients. In addition, we found a significantly reduced density of ABCB1-expressing neurons in the left habenula. Reduced ABCB1 expression in habenular capillaries might contribute to increased brain levels of proinflammatory cytokines in patients with schizophrenia, while decreased expression of this protein in a subpopulation of medial habenular neurons (which are probably purinergic) might be related to abnormalities of purines and their receptors found in this disease.

摘要

越来越多的证据表明,微血管异常和血脑屏障(BBB)功能障碍在精神分裂症的病理生理学中起重要作用。ATP结合盒转运蛋白ABCB1是完整血脑屏障的重要分子成分,它与包括精神分裂症在内的多种神经退行性疾病和精神疾病有关。然而,ABCB1在精神分裂症中的区域和细胞表达尚未得到研究。因此,我们采用免疫组织化学方法研究了13例精神分裂症患者和9例对照者中已知在精神分裂症中起作用的12个人类死后脑区的ABCB1蛋白表达。在研究的12个脑区中的10个脑区,所有精神分裂症患者和对照病例之间,表达ABCB1的毛细血管的数量密度没有发现显著差异。然而,精神分裂症患者的左右缰核复合体显示毛细血管密度显著降低。此外,我们发现左侧缰核中表达ABCB1的神经元密度显著降低。缰核毛细血管中ABCB1表达降低可能导致精神分裂症患者脑内促炎细胞因子水平升高,而内侧缰核神经元亚群(可能是嘌呤能神经元)中该蛋白表达降低可能与该疾病中发现的嘌呤及其受体异常有关。

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