实验动物与比较医学 ›› 2026, Vol. 46 ›› Issue (2): 153-177.DOI: 10.12300/j.issn.1674-5817.2025.073

• 人类疾病动物模型 •    下一篇

帕金森病药物和干细胞治疗临床前动物实验模型选择指南(2026年版)

中国研究型医院学会医学动物实验专家委员会,中国医药生物技术协会再生医学分会韩发彬(), 陈琳(), 陈志国(), 卢明(), 李英俊()   

  • 收稿日期:2025-05-15 修回日期:2025-08-15 出版日期:2026-04-25 发布日期:2026-04-18
  • 通讯作者:
    韩发彬(1962—),男,博士,教授,研究方向:干细胞移植治疗神经疾病研究。E-mail:fhan2013@126.com。ORCID:0000-0003-0220-0471;

    陈 琳(1971—),男,博士,主任医师,研究方向:神经修复学。E-mail:chenlin_china@163.com。ORCID:0000-0002-0725-4156;

    陈志国(1977—),男,博士,教授/研究员,研究方向:干细胞与再生医学及疾病机制研究。E-mail:chenzhiguo@gmail.com。ORCID:0000-0003-1508-510X;

    卢 明(1959—),男,博士,主任医师,研究方向:神经疾病干细胞移植治疗。E-mail:lumingcs163@163.com。ORCID:0000-0002-8275-7490;
    李英俊(1974—),男,博士,教授,研究方向:病理学与病理生理学。E-mail:bjthst@163.com。ORCID:0009-0003-5971-6599

Guidelines for Selecting Preclinical Animal Models for Drugs and Stem Cell Therapies for Parkinson Disease (2026 Edition)

Committee of Experts on Medical Animal Experiments, Chinese Research Hospital Association;
Committee of Regenerative Medicine Branch, Chinese Medicinal Biotech Association
HAN Fabin(), CHEN Lin(), CHEN Zhiguo(), LU Ming(), LI Yingjun()   

摘要:

帕金森病(Parkinson disease,PD)是中老年人群中常见的一种神经退行性变性疾病,其主要临床特征包括静止性震颤、运动迟缓、肢体僵硬以及姿势步态异常。除上述运动障碍外,大部分PD患者还常伴有记忆力减退、抑郁、疼痛、嗅觉减退和睡眠障碍等非运动障碍症状。PD的发病原因尚未完全明确,其主要病理特征是形成以α突触核蛋白为主要成分的路易体。路易体不仅存在于中脑的黑质致密部,还可扩散至迷走神经背核、蓝斑核等脑区,引起多巴胺能神经元的退行性变性。目前PD的诊断主要依赖于患者的临床表现,颅脑CT和磁共振成像检查通常无明显异常。常用的PD治疗药物包括左旋多巴、多巴胺受体激动剂等,其他疗法还有深部脑电刺激和干细胞替代治疗等。由于PD的核心病理改变是中脑特异多巴胺能神经元的数量减少,移植不同来源的神经干细胞或多巴胺能前体细胞成为目前治疗PD最有潜力的方法。无论是药物、器械或细胞移植疗法,在应用于临床前都需要借助PD动物模型进行临床前研究,以验证其有效性和安全性。因此,中国研究型医院学会医学动物实验专家委员会牵头,联合国内高等院校、科研院所和研究型医院的近70位专家,经过4轮论证以及3轮意见征集和编辑修订,制定了本指南。本指南首先概述了PD的病因、临床表现和分子机制,然后重点介绍了常用PD动物模型——包括药物诱导(小鼠、大鼠和非人灵长类)模型和基因修饰(小鼠和大鼠)模型的造模方法、造模机制、模型评估方法和应用范围,并总结了应用这些动物模型进行药物和干细胞治疗临床前评估的基本原则。本指南旨在为PD治疗新药和新技术研发提供动物模型选择的理论和实验指导,同时为建立标准化的PD模型和评价体系提供参考框架。

关键词: 帕金森病, 帕金森病动物模型, 运动障碍, 多巴胺能神经元, 干细胞治疗

Abstract:

Parkinson disease (PD) is a common neurodegenerative disease in middle-aged and elderly people. Its main clinical features include tremor at rest, bradykinesia, limb rigidity, abnormal posture and gait. In addition to motor dysfunction, most PD patients also show non-motor symptoms, including memory impairment, depression, pain, reduced olfaction, and sleep disorders. The etiology of PD has not been fully clarified, and its main pathological feature is the formation of Lewy bodies mainly composed of α-synuclein. Lewy bodies are not only present in the substantia nigra pars compacta of the midbrain, but can also spread to brain regions such as the dorsal motor nucleus of the vagus and the locus coeruleus, leading to degeneration of dopaminergic neurons. The diagnosis of PD mainly depends on clinical manifestations. Cranial CT and magnetic resonance imaging usually show no obvious abnormalities. Commonly used drugs for PD include levodopa and dopamine receptor agonists, and other therapies include deep brain stimulation and stem cell replacement therapy. Because the core pathological change in PD is the loss of midbrain-specific dopaminergic neurons, transplantation of neural stem cells or dopaminergic progenitor cells from different sources is currently the most promising therapeutic approach for PD. Before clinical application, drugs, novel instruments, and cell transplantation therapies all require preclinical studies using PD animal models to verify their efficacy and safety. Therefore, this guideline is developed under the leadership of the Committee of Experts on Medical Animal Experiments of the Chinese Research Hospital Association, in collaboration with nearly 70 experts from domestic universities, research institutes, and research-oriented hospitals, through four rounds of deliberation and three rounds of opinion solicitation and editorial revision. This guideline first reviews the etiology, clinical manifestations, and molecular mechanisms of PD, and then focuses on the commonly used PD animal models—including drug-induced (mouse, rat, and non-human primate) models and transgenic (mouse and rat) models—covering their modeling methods, mechanisms, evaluation approaches, and application scope, and summarizes the basic principles for preclinical evaluation of drug and stem cell therapies using these models. This guideline aims to provide theoretical and experimental guidance for selecting animal models in the development of new drugs and technologies for PD treatment, and to offer a reference framework for establishing standardized PD models and evaluation systems.

Key words: Parkinson disease, Parkinson disease animal model, Motor dysfunction, Dopaminergic neuron, Stem cell therapy

中图分类号: