• 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

特发性帕金森病中的迈内特基底核。

The basal nucleus of Meynert in idiopathic Parkinson's disease.

作者信息

Tagliavini F, Pilleri G, Bouras C, Constantinidis J

出版信息

Acta Neurol Scand. 1984 Jul;70(1):20-8. doi: 10.1111/j.1600-0404.1984.tb00798.x.

DOI:10.1111/j.1600-0404.1984.tb00798.x
PMID:6475484
Abstract

The basal nucleus of Meynert (bnM) was examined in 6 patients with idiopathic Parkinson's disease and in 5 age-matched controls. The histopathological study was followed by a quantitative analysis of the magnocellular population of the nucleus, with the determination of the number of neurons and their nucleolar volume. In Parkinson's disease, there was a neuronal loss ranging from 29.9% to 68.3% (mean 45.8%) and numerous surviving cells containing Lewy inclusion bodies. The percentage loss of cells did not display a significant correlation with the age of the patients, the duration of the illness, the mental state or the drug regime. On the other hand, no significant differences in nucleolar volume of bnM neurons were detected between patients and controls. The damage of the basal nucleus of Meynert in Parkinson's disease is less severe than that generally observed in Alzheimer's disease, and is slightly more pronounced than that reported for progressive supranuclear palsy.

摘要

对6例特发性帕金森病患者和5例年龄匹配的对照者的Meynert基底核(bnM)进行了检查。组织病理学研究之后,对该核的大细胞群体进行了定量分析,测定了神经元数量及其核仁体积。在帕金森病中,神经元丢失率为29.9%至68.3%(平均45.8%),且有大量含有路易小体的存活细胞。细胞丢失百分比与患者年龄、病程、精神状态或用药方案均无显著相关性。另一方面,患者与对照者之间bnM神经元的核仁体积未检测到显著差异。帕金森病中Meynert基底核的损伤程度不如阿尔茨海默病中通常观察到的严重,且比进行性核上性麻痹中报道的损伤稍明显。

相似文献

1
The basal nucleus of Meynert in idiopathic Parkinson's disease.特发性帕金森病中的迈内特基底核。
Acta Neurol Scand. 1984 Jul;70(1):20-8. doi: 10.1111/j.1600-0404.1984.tb00798.x.
2
Parkinson's disease: neuron loss in the nucleus basalis without concomitant Alzheimer's disease.帕金森病:基底核神经元丢失,无阿尔茨海默病伴随
Ann Neurol. 1984 May;15(5):415-8. doi: 10.1002/ana.410150503.
3
The basal nucleus of Meynert in patients with progressive supranuclear palsy.进行性核上性麻痹患者的迈内特基底核。
Neurosci Lett. 1984 Jan 27;44(1):37-42. doi: 10.1016/0304-3940(84)90217-9.
4
Correlative decrease of large neurons in the neostriatum and basal nucleus of Meynert in Alzheimer's disease.阿尔茨海默病中新纹状体和迈内特基底核大神经元的相关性减少。
Brain Res. 1989 Dec 18;504(2):354-7. doi: 10.1016/0006-8993(89)91384-x.
5
A comparison of changes in the nucleus basalis and locus caeruleus in Alzheimer's disease.阿尔茨海默病中基底核与蓝斑核变化的比较。
J Neurol Neurosurg Psychiatry. 1984 Feb;47(2):201-3. doi: 10.1136/jnnp.47.2.201.
6
Clinical and neurochemical consequences of neuronal loss in the nucleus basalis of Meynert in Parkinson's disease and Alzheimer's disease.帕金森病和阿尔茨海默病中迈内特基底核神经元丢失的临床和神经化学后果。
Adv Neurol. 1987;45:393-7.
7
The nucleus basalis of Meynert in neurological disease: a quantitative morphological study.迈内特基底核在神经疾病中的研究:一项定量形态学研究
Ann Neurol. 1985 Feb;17(2):163-70. doi: 10.1002/ana.410170210.
8
The nucleus basalis of Meynert in multi-infarct (vascular) dementia.多梗死性(血管性)痴呆中的迈内特基底核
Acta Neuropathol. 1986;71(3-4):332-7. doi: 10.1007/BF00688058.
9
Galanin hyperinnervates surviving neurons of the human basal nucleus of Meynert in dementias of Alzheimer's and Parkinson's disease: a hypothesis for the role of galanin in accentuating cholinergic dysfunction in dementia.在阿尔茨海默病和帕金森病所致痴呆中,甘丙肽对人类迈内特基底核存活神经元的神经支配增加:甘丙肽在加重痴呆中胆碱能功能障碍作用的一种假说。
J Comp Neurol. 1988 Jul 22;273(4):543-57. doi: 10.1002/cne.902730409.
10
Hyperinnervation of surviving neurons of the human basal nucleus of meynert by galanin in dementias of Alzheimer's and Parkinson's disease.在阿尔茨海默病和帕金森病所致痴呆中,甘丙肽对人类迈内特基底核存活神经元的神经支配过强。
Adv Neurol. 1990;51:253-5.

引用本文的文献

1
Single-nucleus analysis reveals oxidative stress in Down syndrome basal forebrain neurons at birth.单核分析揭示唐氏综合征基底前脑神经元在出生时存在氧化应激。
Alzheimers Dement. 2025 Jul;21(7):e70445. doi: 10.1002/alz.70445.
2
Single-nucleus analysis reveals dysregulated oxidative phosphorylation in Down syndrome basal forebrain at birth.单核分析揭示唐氏综合征出生时基底前脑氧化磷酸化失调。
bioRxiv. 2025 Feb 6:2025.02.05.636750. doi: 10.1101/2025.02.05.636750.
3
Parkinson's Disease Mild Cognitive Impairment with MRI evidence of Cholinergic Nucleus 4 Degeneration: A New Subtype?
伴有胆碱能核4变性MRI证据的帕金森病轻度认知障碍:一种新亚型?
Res Sq. 2024 Nov 11:rs.3.rs-5278177. doi: 10.21203/rs.3.rs-5278177/v1.
4
Cholinergic Basal Forebrain Integrity and Cognition in Parkinson's Disease: A Reappraisal of Magnetic Resonance Imaging Evidence.帕金森病中胆碱能基底前脑完整性与认知:对磁共振成像证据的重新评估
Mov Disord. 2024 Dec;39(12):2155-2172. doi: 10.1002/mds.30023. Epub 2024 Oct 3.
5
Neurotrophin mimetics and tropomyosin kinase receptors: a futuristic pharmacological tool for Parkinson's.神经营养因子模拟物和原肌球蛋白激酶受体:治疗帕金森病的未来药物靶点。
Neurol Sci. 2023 Jul;44(7):2265-2275. doi: 10.1007/s10072-023-06684-1. Epub 2023 Mar 4.
6
Imaging Cognitive Impairment and Impulse Control Disorders in Parkinson's Disease.帕金森病中的认知障碍与冲动控制障碍成像
Front Neurol. 2021 Nov 5;12:733570. doi: 10.3389/fneur.2021.733570. eCollection 2021.
7
The Cholinergic Brain in Parkinson's Disease.帕金森病中的胆碱能脑
Mov Disord Clin Pract. 2021 Aug 23;8(7):1012-1026. doi: 10.1002/mdc3.13319. eCollection 2021 Oct.
8
Basal forebrain cholinergic system in the dementias: Vulnerability, resilience, and resistance.痴呆症中的基底前脑胆碱能系统:脆弱性、弹性和抗性。
J Neurochem. 2021 Sep;158(6):1394-1411. doi: 10.1111/jnc.15471. Epub 2021 Aug 6.
9
On Cell Loss and Selective Vulnerability of Neuronal Populations in Parkinson's Disease.帕金森病中神经元群体的细胞丢失与选择性易损性
Front Neurol. 2018 Jun 19;9:455. doi: 10.3389/fneur.2018.00455. eCollection 2018.
10
Chronic MPTP administration regimen in monkeys: a model of dopaminergic and non-dopaminergic cell loss in Parkinson's disease.慢性 MPTP 给药方案在猴子中的应用:帕金森病多巴胺能和非多巴胺能细胞丧失的模型。
J Neural Transm (Vienna). 2018 Mar;125(3):337-363. doi: 10.1007/s00702-017-1774-z. Epub 2017 Aug 31.