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本文引用的文献

1
Differential pathological dynamics triggered by distinct Parkinson patient-derived α-synuclein extracts in nonhuman primates.不同帕金森病患者来源的α-突触核蛋白提取物在非人灵长类动物中引发的不同病理动力学。
Sci Adv. 2025 Jun 20;11(25):eadu6050. doi: 10.1126/sciadv.adu6050. Epub 2025 Jun 18.
2
A human brain map of mitochondrial respiratory capacity and diversity.线粒体呼吸能力与多样性的人脑图谱。
Nature. 2025 May;641(8063):749-758. doi: 10.1038/s41586-025-08740-6. Epub 2025 Mar 26.
3
Expression patterns of blood-based biomarkers of neurodegeneration and inflammation across adulthood in rhesus macaques.成年恒河猴神经退行性变和炎症的血液生物标志物表达模式。
Exp Gerontol. 2025 May;203:112736. doi: 10.1016/j.exger.2025.112736. Epub 2025 Mar 21.
4
Brain aging and Alzheimer's disease, a perspective from non-human primates.脑衰老与阿尔茨海默病:非人灵长类动物的视角。
Aging (Albany NY). 2024 Oct 29;16(20):13145-13171. doi: 10.18632/aging.206143.
5
Modeling Parkinson's Disease in Primates.灵长类动物帕金森病模型
Cold Spring Harb Perspect Med. 2025 Feb 3;15(2):a041612. doi: 10.1101/cshperspect.a041612.
6
Neuromelanin accumulation drives endogenous synucleinopathy in non-human primates.神经黑色素积累导致非人类灵长类动物的内源性突触核蛋白病。
Brain. 2023 Dec 1;146(12):5000-5014. doi: 10.1093/brain/awad331.
7
Functional and neuropathological changes induced by injection of distinct alpha-synuclein strains: A pilot study in non-human primates.不同α-突触核蛋白菌株注射引起的功能和神经病理学变化:非人类灵长类动物的初步研究。
Neurobiol Dis. 2023 May;180:106086. doi: 10.1016/j.nbd.2023.106086. Epub 2023 Mar 17.
8
Reframing the perception of outliers and negative data in translational research.重新构建转化研究中外显子和负性数据的认知。
Brain Res Bull. 2023 Jan;192:203-207. doi: 10.1016/j.brainresbull.2022.11.020. Epub 2022 Dec 1.
9
Gene editing monkeys: Retrospect and outlook.基因编辑猴子:回顾与展望。
Front Cell Dev Biol. 2022 Sep 8;10:913996. doi: 10.3389/fcell.2022.913996. eCollection 2022.
10
Lewy Body Disease Primate Model with α-Synuclein Propagation from the Olfactory Bulb.路易体病灵长类模型中嗅球α-突触核蛋白的传播。
Mov Disord. 2022 Oct;37(10):2033-2044. doi: 10.1002/mds.29161. Epub 2022 Aug 21.

立场文件:利用非人灵长类动物(NHP)的特性加速帕金森病和衰老研究。

Position paper: leveraging non-human primate (NHP) specificities to accelerate Parkinson's disease and ageing research.

作者信息

Bezard Erwan, Anderson Rozalyn M, Badin Romina Aron, Bergman Hagai, Boehringer Ashley, Borgognon Simon, Emborg Marina E, Kordower Jeffrey H, Li Jia-Yi, Martel Anne-Caroline, Metzger Jeanette M, Smith Yoland, Takada Masahiko, Takahashi Jun, Takahashi Ryosuke, Dehay Benjamin

机构信息

Univ. Bordeaux, CNRS, IMN, UMR 5293, F-33000, Bordeaux, France.

Division of Geriatrics, Department of Medicine, SMPH, University of Wisconsin-Madison, & GRECC, William S Middleton Memorial Veterans Hospital, Madison, WI, USA.

出版信息

NPJ Parkinsons Dis. 2025 Aug 2;11(1):227. doi: 10.1038/s41531-025-01088-8.

DOI:10.1038/s41531-025-01088-8
PMID:40753086
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12317990/
Abstract

The PD-AGE international task force underscores the pivotal role that non-human primate (NHP) models play in advancing our understanding of Parkinson's disease (PD) and ageing. Due to their close genetic, anatomical, and behavioural similarity to humans, NHPs uniquely enable translational research to bridge basic science towards clinical application. They are indispensable for modelling the complex motor and non-motor symptoms of PD, as well as age-related neurodegeneration. This paper outlines the scientific rationale, methodological strengths, and ethical considerations surrounding NHP use in PD research. We highlight the need for standardised models, innovative tools, and long-term collaborative infrastructure to enhance the translational value of NHP studies. We propose a three-phase roadmap to develop a global research consortium to optimise resource use, improve model fidelity, and accelerate therapeutic development for PD and related neurodegenerative disorders.

摘要

帕金森病与衰老国际特别工作组强调了非人灵长类动物(NHP)模型在增进我们对帕金森病(PD)和衰老的理解方面所发挥的关键作用。由于它们在基因、解剖结构和行为上与人类高度相似,非人灵长类动物为将基础科学转化为临床应用的转化研究提供了独特的条件。它们对于模拟帕金森病复杂的运动和非运动症状以及与年龄相关的神经退行性变至关重要。本文概述了在帕金森病研究中使用非人灵长类动物的科学依据、方法优势和伦理考量。我们强调需要标准化模型、创新工具和长期协作基础设施,以提高非人灵长类动物研究的转化价值。我们提出了一个三阶段路线图,以建立一个全球研究联盟,优化资源利用,提高模型保真度,并加速针对帕金森病及相关神经退行性疾病的治疗开发。