• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

多巴胺神经元为了生存而需要刺激的特定需求:对帕金森病的启示。

Specific needs of dopamine neurons for stimulation in order to survive: implication for Parkinson disease.

机构信息

Université Pierre et Marie Curie-Paris 6, Centre de Recherche de l'Institut du Cerveau et de la Moelle Epinière, Unité Mixte de Recherche (UMR) S975, Paris, France.

出版信息

FASEB J. 2013 Sep;27(9):3414-23. doi: 10.1096/fj.12-220418. Epub 2013 May 22.

DOI:10.1096/fj.12-220418
PMID:23699175
Abstract

Parkinson disease (PD) is a degenerative brain disorder characterized by motor symptoms that are unequivocally associated with the loss of dopaminergic (DA) neurons in the substantia nigra (SN). Although our knowledge of the mechanisms that contribute to DA cell death in both hereditary and sporadic forms of the disease has advanced significantly, the nature of the pathogenic process remains poorly understood. In this review, we present evidence that neurodegeneration occurs when the electrical activity and excitability of these neurons is reduced. In particular, we will focus on the specific need these neurons may have for stimulation in order to survive and on the molecular and cellular mechanisms that may be compromised when this need is no longer met in PD.

摘要

帕金森病(PD)是一种退行性脑疾病,其特征为运动症状,这些症状与黑质(SN)中多巴胺能(DA)神经元的丧失明确相关。尽管我们对导致遗传性和散发性疾病中 DA 细胞死亡的机制的了解有了显著进展,但发病过程的本质仍知之甚少。在这篇综述中,我们提出证据表明,当这些神经元的电活动和兴奋性降低时,神经退行性变就会发生。特别是,我们将重点关注这些神经元为了生存可能需要刺激的特定需求,以及当这种需求在 PD 中不再得到满足时可能受到损害的分子和细胞机制。

相似文献

1
Specific needs of dopamine neurons for stimulation in order to survive: implication for Parkinson disease.多巴胺神经元为了生存而需要刺激的特定需求:对帕金森病的启示。
FASEB J. 2013 Sep;27(9):3414-23. doi: 10.1096/fj.12-220418. Epub 2013 May 22.
2
Understanding Dopaminergic Cell Death Pathways in Parkinson Disease.了解帕金森病中的多巴胺能细胞死亡途径。
Neuron. 2016 May 18;90(4):675-91. doi: 10.1016/j.neuron.2016.03.038.
3
Accumulation of mitochondrial DNA deletions within dopaminergic neurons triggers neuroprotective mechanisms.线粒体 DNA 缺失在多巴胺能神经元内的积累引发神经保护机制。
Brain. 2013 Aug;136(Pt 8):2369-78. doi: 10.1093/brain/awt196.
4
Subthalamic GAD gene transfer in Parkinson disease patients who are candidates for deep brain stimulation.对适合进行深部脑刺激的帕金森病患者进行丘脑底核谷氨酸脱羧酶基因转移。
Hum Gene Ther. 2001 Aug 10;12(12):1589-91.
5
Dopamine receptor D3 expressed on CD4+ T cells favors neurodegeneration of dopaminergic neurons during Parkinson's disease.CD4+T 细胞上表达的多巴胺受体 D3 在帕金森病中有利于多巴胺能神经元的神经退行性变。
J Immunol. 2013 May 15;190(10):5048-56. doi: 10.4049/jimmunol.1203121. Epub 2013 Apr 15.
6
Interaction of alpha-synuclein and dopamine metabolites in the pathogenesis of Parkinson's disease: a case for the selective vulnerability of the substantia nigra.α-突触核蛋白与多巴胺代谢产物在帕金森病发病机制中的相互作用:黑质选择性易损性的实例
Acta Neuropathol. 2006 Aug;112(2):115-26. doi: 10.1007/s00401-006-0096-2. Epub 2006 Jun 22.
7
Neuronal vulnerability in Parkinson's disease.帕金森病中的神经元易损性。
Parkinsonism Relat Disord. 2012 Jan;18 Suppl 1:S52-4. doi: 10.1016/S1353-8020(11)70018-9.
8
Can mesenchymal stem cells reduce vulnerability of dopaminergic neurons in the substantia nigra to oxidative insult in individuals at risk to Parkinson's disease?间充质干细胞能否降低帕金森病高危个体黑质多巴胺能神经元对氧化应激的易损性?
Cell Biol Int. 2012 Jul;36(7):617-24. doi: 10.1042/CBI20110602.
9
Dopaminergic neurons reduced to silence by oxidative stress: an early step in the death cascade in Parkinson's disease?多巴胺能神经元因氧化应激而沉默:帕金森病死亡级联反应的早期步骤?
Sci STKE. 2006 Apr 25;2006(332):pe19. doi: 10.1126/stke.3322006pe19.
10
Mitochondria, calcium, and endoplasmic reticulum stress in Parkinson's disease.线粒体、钙和内质网应激与帕金森病。
Biofactors. 2011 May-Jun;37(3):228-40. doi: 10.1002/biof.159. Epub 2011 Jun 14.

引用本文的文献

1
GDNF receptor GFRα1 is necessary for the maintenance of dopaminergic neurons in the adult substantia nigra.胶质细胞源性神经营养因子受体GFRα1对于成年黑质中多巴胺能神经元的维持是必需的。
PLoS One. 2025 Sep 4;20(9):e0331369. doi: 10.1371/journal.pone.0331369. eCollection 2025.
2
Neurotransmitters' white matter mapping unveils the neurochemical fingerprints of stroke.神经递质的白质图谱揭示了中风的神经化学指纹。
Nat Commun. 2025 Mar 15;16(1):2555. doi: 10.1038/s41467-025-57680-2.
3
Astrocytic Calcium and cAMP in Neurodegenerative Diseases.
神经退行性疾病中的星形胶质细胞钙和环磷酸腺苷
Front Cell Neurosci. 2022 May 19;16:889939. doi: 10.3389/fncel.2022.889939. eCollection 2022.
4
GLP-1 Suppresses Feeding Behaviors and Modulates Neuronal Electrophysiological Properties in Multiple Brain Regions.胰高血糖素样肽-1抑制摄食行为并调节多个脑区的神经元电生理特性。
Front Mol Neurosci. 2021 Dec 17;14:793004. doi: 10.3389/fnmol.2021.793004. eCollection 2021.
5
Functional Importance of Transient Receptor Potential (TRP) Channels in Neurological Disorders.瞬时受体电位(TRP)通道在神经系统疾病中的功能重要性
Front Cell Dev Biol. 2021 Mar 4;9:611773. doi: 10.3389/fcell.2021.611773. eCollection 2021.
6
Allosterism of Nicotinic Acetylcholine Receptors: Therapeutic Potential for Neuroinflammation Underlying Brain Trauma and Degenerative Disorders.乙酰胆碱受体变构调节:脑创伤和退行性疾病相关神经炎症的治疗潜力。
Int J Mol Sci. 2020 Jul 12;21(14):4918. doi: 10.3390/ijms21144918.
7
TRP Channels as Emerging Therapeutic Targets for Neurodegenerative Diseases.瞬时受体电位通道作为神经退行性疾病的新兴治疗靶点
Front Physiol. 2020 Apr 15;11:238. doi: 10.3389/fphys.2020.00238. eCollection 2020.
8
Neuroprotective Mechanisms of Three Natural Antioxidants on a Rat Model of Parkinson's Disease: A Comparative Study.三种天然抗氧化剂对帕金森病大鼠模型的神经保护机制:一项比较研究
Antioxidants (Basel). 2020 Jan 6;9(1):49. doi: 10.3390/antiox9010049.
9
Critical Role of Oxidatively Damaged DNA in Selective Noradrenergic Vulnerability.氧化损伤 DNA 在选择性去甲肾上腺素能易损性中的关键作用。
Neuroscience. 2019 Dec 1;422:184-201. doi: 10.1016/j.neuroscience.2019.09.036. Epub 2019 Nov 5.
10
Nurr1, Pitx3, and α7 nAChRs mRNA Expression in Nigral Tissue of Rats with Pedunculopontine Neurotoxic Lesion.红核神经元转录因子 1、pituitary homeobox 3 和 α7 烟碱型乙酰胆碱受体 mRNA 在被脑桥被盖部神经毒损伤的大鼠黑质组织中的表达。
Medicina (Kaunas). 2019 Sep 20;55(10):616. doi: 10.3390/medicina55100616.