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p75NTR 作为神经精神疾病的治疗靶点。

p75NTR as a therapeutic target for neuropsychiatric diseases.

机构信息

Department of Mental Disorder Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo, 187-8502, Japan.

出版信息

Curr Mol Pharmacol. 2009 Jan;2(1):70-6. doi: 10.2174/1874467210902010070.

Abstract

The p75 neurotrophin receptor (p75NTR) was originally identified as a low-affinity receptor for neurotrophins. Recent studies have revealed that p75NTR can promote cell death or survival and modulate neurite outgrowth depending on the operative ligands and co-receptors. Up-regulation and ligand activation of p75NTR have been shown to be involved in neuronal cell death in cultured cells and animal models of neurodegenerative diseases. The levels of proneurotrophins, which bind to p75NTR to promote neuronal death, have been found to be increased in postmortem brains of patients with Alzheimer's disease. Furthermore, there is some evidence for the involvement of this molecule in psychiatric diseases, such as depression and schizophrenia. Mice lacking p75NTR have been shown to have several alterations in central nervous system and cognitive function. Notably, recent progress in genome-based drug discovery has enabled the identification of peptides and non-peptide small molecules targeting p75NTR, which may be potentially beneficial in the treatment of neuropsychiatric diseases. In this review, we focus on recent findings on p75NTR as a therapeutic target for neuropsychiatric diseases.

摘要

p75 神经营养因子受体(p75NTR)最初被鉴定为神经营养因子的低亲和力受体。最近的研究表明,p75NTR 可以根据作用配体和共受体促进细胞死亡或存活,并调节轴突生长。在培养细胞和神经退行性疾病动物模型中,已经证明 p75NTR 的上调和配体激活参与神经元细胞死亡。在阿尔茨海默病患者的尸检大脑中发现,与 p75NTR 结合促进神经元死亡的前神经生长因子的水平增加。此外,有一些证据表明该分子参与了精神疾病,如抑郁症和精神分裂症。缺乏 p75NTR 的小鼠表现出中枢神经系统和认知功能的多种改变。值得注意的是,基于基因组的药物发现的最新进展使得能够鉴定针对 p75NTR 的肽和非肽小分子,它们可能对治疗神经精神疾病有益。在这篇综述中,我们重点介绍了 p75NTR 作为神经精神疾病治疗靶点的最新发现。

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