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胶质细胞源性神经营养因子和转化生长因子β1 的抗帕金森营养作用在大鼠共输注后增强。

Antiparkinsonian trophic action of glial cell line-derived neurotrophic factor and transforming growth factor β1 is enhanced after co-infusion in rats.

机构信息

Departamento de Fisiologia Medica y Biofisica, Universidad de Sevilla, Av. Sanchez Pizjuan 4, 41009 Sevilla, Spain.

出版信息

Exp Neurol. 2010 Nov;226(1):136-47. doi: 10.1016/j.expneurol.2010.08.016. Epub 2010 Aug 14.

Abstract

The objective was to analyze functional effects of the combination of GDNF and TGF-β1 in the retrograde model of Parkinsonism in rats, based on the intrastriatal infusion of 6-hydroxydopamine, which leads to protracted and progressive cell death in the substantia nigra. Hemiparkinsonian rats were implanted with osmotic minipumps 2 months after striatal lesion, pumps delivering GDNF alone (10 ng/day), TGF-β1 alone (2 ng/day), or a GDNF and TGF-β1 combination. The findings confirmed that GDNF alone has potent dopaminotrophic effects but they also revealed, for the first time, that GDNF and TGF-β1 co-infusion led to stronger trophic effects relative to the infusion of GDNF alone. TGF-β1 allowed further reducing dopamine receptor hypersensitivity, and potentiated GDNF-mediated effects. This cooperation could be accounted for by the recruitment of GFRα1 on striatal membranes, and by enhanced expression and activation of TH through augmented pSer31TH and pSer40TH. Co-infusion induced striatal sprouting, as revealed by augmentation of p21-Arc, stathmin, and synaptophysin, and led to a reliable recovery of phenotypic expression of TH in surviving nigral neurons. Functional recovery and improvement of TH signal in the nigrostriatal system were long-lasting and sustained, remaining after cessation of trophic infusion.

摘要

目的在于分析 GDNF 和 TGF-β1 联合应用在大鼠帕金森病逆行模型中的功能效应,该模型基于纹状体中 6-羟多巴胺的注入,导致黑质神经元进行性和持续性死亡。半侧帕金森大鼠在纹状体损伤后 2 个月植入渗透微型泵,泵内分别输送 GDNF(10ng/天)、TGF-β1(2ng/天)或 GDNF 和 TGF-β1 联合。研究结果证实 GDNF 具有很强的多巴胺能营养作用,但也首次表明 GDNF 和 TGF-β1 联合输注相对于单独输注 GDNF 具有更强的营养作用。TGF-β1 进一步减轻多巴胺受体超敏性,并增强 GDNF 介导的作用。这种协同作用可以通过 GFRα1 在纹状体膜上的募集以及通过增强的 pSer31TH 和 pSer40TH 来解释,从而增强 TH 的表达和激活。联合输注诱导纹状体发芽,表现为 p21-Arc、stathmin 和突触小体素的增加,并导致存活的黑质神经元中 TH 的表型表达可靠恢复。黑质纹状体系统中的功能恢复和 TH 信号的改善是持久的,在营养输注停止后仍然存在。

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