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本文引用的文献

1
Naringin: a protector of the nigrostriatal dopaminergic projection.柚皮苷:黑质纹状体多巴胺能投射的保护者。
Exp Neurobiol. 2014 Jun;23(2):124-9. doi: 10.5607/en.2014.23.2.124. Epub 2014 Jun 13.
2
Induction of GDNF and BDNF by hRheb(S16H) transduction of SNpc neurons: neuroprotective mechanisms of hRheb(S16H) in a model of Parkinson's disease.通过向黑质致密部神经元转导hRheb(S16H)诱导胶质细胞源性神经营养因子(GDNF)和脑源性神经营养因子(BDNF):帕金森病模型中hRheb(S16H)的神经保护机制
Mol Neurobiol. 2015 Apr;51(2):487-99. doi: 10.1007/s12035-014-8729-2. Epub 2014 May 25.
3
Naringin protects the nigrostriatal dopaminergic projection through induction of GDNF in a neurotoxin model of Parkinson's disease.柚皮苷通过在帕金森病神经毒素模型中诱导 GDNF 来保护黑质纹状体多巴胺能投射。
J Nutr Biochem. 2014 Jul;25(7):801-6. doi: 10.1016/j.jnutbio.2014.03.006. Epub 2014 Apr 1.
4
Parkinson's disease gene therapy: success by design meets failure by efficacy.帕金森病基因治疗:设计上的成功与疗效上的失败相遇。
Mol Ther. 2014 Mar;22(3):487-497. doi: 10.1038/mt.2013.281. Epub 2013 Dec 20.
5
AAV2-mediated striatum delivery of human CDNF prevents the deterioration of midbrain dopamine neurons in a 6-hydroxydopamine induced parkinsonian rat model.腺相关病毒 2 介导的纹状体递送人神经细胞营养因子可预防 6-羟多巴胺诱导的帕金森病大鼠模型中中脑多巴胺神经元的恶化。
Exp Neurol. 2013 Oct;248:148-56. doi: 10.1016/j.expneurol.2013.06.002. Epub 2013 Jun 10.
6
GDNF, NGF and BDNF as therapeutic options for neurodegeneration.GDNF、NGF 和 BDNF 作为神经退行性疾病的治疗选择。
Pharmacol Ther. 2013 May;138(2):155-75. doi: 10.1016/j.pharmthera.2013.01.004. Epub 2013 Jan 21.
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Parkinson's disease: gene therapies.帕金森病:基因疗法。
Cold Spring Harb Perspect Med. 2012 Apr;2(4):a009431. doi: 10.1101/cshperspect.a009431.
8
Neurotoxin-induced ER stress in mouse dopaminergic neurons involves downregulation of TRPC1 and inhibition of AKT/mTOR signaling.神经毒素诱导的小鼠多巴胺能神经元内质网应激涉及 TRPC1 的下调和 AKT/mTOR 信号的抑制。
J Clin Invest. 2012 Apr;122(4):1354-67. doi: 10.1172/JCI61332. Epub 2012 Mar 26.
9
Axon degeneration in Parkinson's disease.帕金森病中的轴突变性。
Exp Neurol. 2013 Aug;246:72-83. doi: 10.1016/j.expneurol.2012.01.011. Epub 2012 Jan 18.
10
AAV transduction of dopamine neurons with constitutively active Rheb protects from neurodegeneration and mediates axon regrowth.AAV 转导具有组成型激活 Rheb 的多巴胺神经元可防止神经退行性变并介导轴突再生。
Mol Ther. 2012 Feb;20(2):275-86. doi: 10.1038/mt.2011.213. Epub 2011 Oct 18.

Rheb(S16H)在黑质致密部多巴胺能神经元中的作用

Roles of Rheb(S16H) in substantia nigra pars compacta dopaminergic neurons .

作者信息

Jeon Min-Tae, Kim Sang Ryong

机构信息

School of Life Sciences, Kyungpook National University, Daegu 700-842, Republic of Korea ; BK21 plus KNU Creative BioResearch Group, Kyungpook National University, Daegu 700-842, Republic of Korea.

School of Life Sciences, Kyungpook National University, Daegu 700-842, Republic of Korea ; BK21 plus KNU Creative BioResearch Group, Kyungpook National University, Daegu 700-842, Republic of Korea ; Institute of Life Science and Biotechnology, Kyungpook National University, Daegu 702-701, Republic of Korea ; Brain Science and Engineering Institute, Kyungpook National University, Daegu 700-842, Republic of Korea.

出版信息

Biomed Rep. 2015 Mar;3(2):137-140. doi: 10.3892/br.2014.397. Epub 2014 Dec 9.

DOI:10.3892/br.2014.397
PMID:25798236
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4360870/
Abstract

Although there are ongoing intensive research efforts, no effective pharmacological therapies for Parkinson's disease (PD) have been developed thus far. However, with the development of efficient gene delivery systems, gene therapy for PD has become a focus of research and increasing evidence suggests that continuous production of neurotrophic factors play a significant role in the functional restoration of the nigrostriatal dopaminergic (DA) system. Our recent study reported that the transduction of DA neurons with ras homolog enriched in brain, which has an S16H mutation [Rheb(S16H)], protected the nigrostriatal DA projection in a neurotoxin model of PD . In addition, Rheb(S16H) expression significantly increased the levels of glial cell line-derived neurotrophic factor and brain-derived neurotrophic factor, which contributed to the neuroprotective effects of Rheb(S16H) in DA neurons in the adult brain, indicating that the activation of the signaling pathways involved in cell survival by a specific gene delivery, such as Rheb(S16H) to adult neurons, may be a useful strategy to protect neural systems in the adult brain. In the present study, a brief overview of our recent studies is provided, which demonstrates the neuroprotective mechanisms of Rheb(S16H) on the nigrostriatal DA projection in the adult brain.

摘要

尽管目前正在进行深入的研究,但迄今为止尚未开发出针对帕金森病(PD)的有效药物治疗方法。然而,随着高效基因递送系统的发展,PD的基因治疗已成为研究热点,越来越多的证据表明神经营养因子的持续产生在黑质纹状体多巴胺能(DA)系统的功能恢复中起重要作用。我们最近的研究报告称,用富含脑的ras同源物(具有S16H突变[Rheb(S16H)])转导DA神经元,在PD神经毒素模型中保护了黑质纹状体DA投射。此外,Rheb(S16H)的表达显著增加了胶质细胞系源性神经营养因子和脑源性神经营养因子的水平,这有助于Rheb(S16H)对成年大脑DA神经元的神经保护作用,表明通过特定基因递送(如将Rheb(S16H)递送至成年神经元)激活细胞存活相关信号通路可能是保护成年大脑神经系统的有用策略。在本研究中,对我们最近的研究进行了简要概述,展示了Rheb(S16H)对成年大脑黑质纹状体DA投射的神经保护机制。