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转位蛋白(18 kDa)配体在精神疾病和神经退行性疾病实验模型中的治疗作用。

Therapeutic actions of translocator protein (18 kDa) ligands in experimental models of psychiatric disorders and neurodegenerative diseases.

作者信息

Arbo B D, Benetti F, Garcia-Segura L M, Ribeiro M F

机构信息

Laboratório de Interação Neuro-Humoral, Department of Physiology, ICBS, Universidade Federal do Rio Grande do Sul (UFRGS), Rua Sarmento Leite, 500, CEP 90050-170 Porto Alegre, RS, Brazil; Cajal Institute, CSIC, Avenida Doctor Arce, 37, 28002 Madrid, Spain.

Laboratório de Neurofisiologia Cognitiva e do Desenvolvimento, Department of Physiology, ICBS, Universidade Federal do Rio Grande do Sul (UFRGS), Rua Sarmento Leite, 500, CEP 90050-170 Porto Alegre, RS, Brazil.

出版信息

J Steroid Biochem Mol Biol. 2015 Nov;154:68-74. doi: 10.1016/j.jsbmb.2015.07.007. Epub 2015 Jul 19.

Abstract

Translocator protein (TSPO) is an 18kDa protein located at contact sites between the outer and the inner mitochondrial membrane. Numerous studies have associated TSPO with the translocation of cholesterol across the aqueous mitochondrial intermembrane space and the regulation of steroidogenesis, as well as with the control of some other mitochondrial functions, such as mitochondrial respiration, mitochondrial permeability transition pore opening, apoptosis and cell proliferation. In the brain, changes in TSPO expression occur in several neuropathological conditions including neurodegenerative diseases and psychiatric disorders. Furthermore, TSPO ligands have been shown to promote neuroprotection in animal models of brain pathology. At least in some cases, the mechanisms of neuroprotection are associated with modifications in brain steroidogenesis. In addition, regulation of neuroinflammation seems to be a common mechanism in the neuroprotective actions of TSPO ligands in different animal models of brain pathology.

摘要

转位蛋白(TSPO)是一种18kDa的蛋白质,位于线粒体外膜与内膜的接触部位。大量研究表明,TSPO与胆固醇在线粒体内膜间隙的转运、类固醇生成的调节有关,还与其他一些线粒体功能的控制有关,如线粒体呼吸、线粒体通透性转换孔开放、细胞凋亡和细胞增殖。在大脑中,TSPO表达的变化出现在多种神经病理状态下,包括神经退行性疾病和精神障碍。此外,TSPO配体已被证明在脑病理动物模型中具有神经保护作用。至少在某些情况下,神经保护机制与脑类固醇生成的改变有关。此外,在不同的脑病理动物模型中,神经炎症的调节似乎是TSPO配体神经保护作用中的一种常见机制。

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