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6-羟多巴胺在体内诱导大鼠黑质纹状体系统中 GDF5 和 GDNF mRNA 表达的明显改变。

6-Hydroxydopamine induces distinct alterations in GDF5 and GDNF mRNA expression in the rat nigrostriatal system in vivo.

机构信息

Department of Anatomy and Neuroscience, Biosciences Institute, University College Cork, Cork, Ireland.

School of Biosciences, Cardiff University, Museum Avenue, Cardiff CF10 3AX, UK.

出版信息

Neurosci Lett. 2014 Feb 21;561:176-81. doi: 10.1016/j.neulet.2013.12.046. Epub 2013 Dec 25.

DOI:10.1016/j.neulet.2013.12.046
PMID:24373993
Abstract

Growth/differentiation factor (GDF)5 and glial cell line-derived neurotrophic factor (GDNF) are neurotrophic factors that promote the survival of midbrain dopaminergic neurons in vitro and in vivo. Both factors have potent neurotrophic and neuroprotective effects in rat models of Parkinson's disease (PD) and represent promising new therapies for PD. The aim of this study was to investigate the expression of GDF5, GDNF and their receptors in the nigrostriatal dopaminergic system in rat models of PD. It found that endogenous GDF5, GDNF and their receptors are differentially expressed in two 6-hydroxydopamine lesion models of PD. In both striatal and medial forebrain bundle (MFB) lesion models, striatal levels of GDF5 mRNA increased at 10 days post-lesion, while GDNF mRNA levels in the nigrostriatal system decreased after 10 and 28 days. Midbrain mRNA levels for both GDF5 receptors transiently increased after striatal lesion, whereas those of two GDNF receptors decreased at later time-points in both models. Despite the fact that exogenous GDF5 and GDNF have comparable effects on dopaminergic neurons in vitro and in vivo, their endogenous responses to neurotoxic injury are different. This highlights the importance of studying neurotrophic factor expression at distinct disease stages and in various animal models of PD.

摘要

生长/分化因子 (GDF)5 和胶质细胞源性神经营养因子 (GDNF) 是神经营养因子,可促进中脑多巴胺能神经元在体外和体内的存活。这两种因子在帕金森病 (PD) 的大鼠模型中均具有强大的神经营养和神经保护作用,是 PD 有前途的新疗法。本研究旨在研究 GDF5、GDNF 及其受体在 PD 大鼠模型黑质纹状体多巴胺能系统中的表达。研究发现,内源性 GDF5、GDNF 及其受体在两种 6-羟多巴胺损伤 PD 模型中表达不同。在纹状体和中脑束 (MFB) 损伤模型中,纹状体 GDF5mRNA 的水平在损伤后 10 天增加,而黑质纹状体系统中的 GDNFmRNA 水平在 10 和 28 天后下降。两种 GDF5 受体的中脑 mRNA 水平在纹状体损伤后短暂增加,而两种 GDNF 受体的水平在两种模型的后期下降。尽管外源性 GDF5 和 GDNF 在体外和体内对多巴胺能神经元具有相似的作用,但它们对神经毒性损伤的内源性反应不同。这突出表明在不同的疾病阶段和各种 PD 动物模型中研究神经营养因子表达的重要性。

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引用本文的文献

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Expression of endogenous Mkp1 in 6-OHDA rat models of Parkinson's disease.帕金森病6-羟多巴胺大鼠模型中内源性Mkp1的表达
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Roles for the TGFβ superfamily in the development and survival of midbrain dopaminergic neurons.
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Mol Neurobiol. 2014 Oct;50(2):559-73. doi: 10.1007/s12035-014-8639-3. Epub 2014 Feb 7.