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犬尿氨酸途径酶色氨酸2,3-双加氧酶的表达在精神分裂症患者的额叶皮质中增加。

Expression of the kynurenine pathway enzyme tryptophan 2,3-dioxygenase is increased in the frontal cortex of individuals with schizophrenia.

作者信息

Miller Christine L, Llenos Ida C, Dulay Jeanette R, Barillo Meliza M, Yolken Robert H, Weis Serge

机构信息

Stanley Division for Developmental Neurovirology, Department of Pediatrics, Johns Hopkins University, Baltimore, MD 21287, USA.

出版信息

Neurobiol Dis. 2004 Apr;15(3):618-29. doi: 10.1016/j.nbd.2003.12.015.

Abstract

Markers of the kynurenine pathway were studied in postmortem frontal cortex obtained from individuals with schizophrenia and controls. Quantitative endpoint RT-PCR was used to measure mRNA transcripts. Of the two enzymes capable of catalyzing the first step in the pathway, tryptophan 2,3-dioxygenase (TDO2) and indoleamine dioxygenase (IDO), the concentration of mRNA for TDO2 was found to be elevated 1.6-fold in the schizophrenia group (P = 0.03), whereas the concentration of the mRNA for IDO was not significantly different between the schizophrenia and control groups. Immunohistochemistry showed an increased density of TDO2-immunopositive astroglial cells in the white matter of patients with schizophrenia (P = 0.04). Neurons and vessels were also immunopositive for TDO2, but there were no significant differences in labeling of these structures between the two groups. These results add to the evidence that kynurenine pathway changes might be involved in the pathogenesis of schizophrenia and the schizophrenia-like psychoses of other disorders.

摘要

在取自精神分裂症患者及对照者的尸检额叶皮质中,对犬尿氨酸途径的标志物进行了研究。采用定量终点逆转录聚合酶链反应(RT-PCR)来测量信使核糖核酸(mRNA)转录本。在能够催化该途径第一步反应的两种酶——色氨酸2,3-双加氧酶(TDO2)和吲哚胺双加氧酶(IDO)中,发现精神分裂症组中TDO2的mRNA浓度升高了1.6倍(P = 0.03),而精神分裂症组与对照组之间IDO的mRNA浓度无显著差异。免疫组织化学显示,精神分裂症患者白质中TDO2免疫阳性星形胶质细胞的密度增加(P = 0.04)。神经元和血管对TDO2也呈免疫阳性,但两组之间这些结构的标记无显著差异。这些结果进一步证明,犬尿氨酸途径的改变可能参与了精神分裂症以及其他疾病的精神分裂症样精神病的发病机制。

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