Laboratory Animal and Comparative Medicine ›› 2026, Vol. 46 ›› Issue (2): 153-177.DOI: 10.12300/j.issn.1674-5817.2025.073
• Animal Models of Human Diseases • Next Articles
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(
)
Received:2025-05-15
Revised:2025-08-15
Online:2026-04-25
Published:2026-04-18
Correspondence to:
HAN Fabin, CHEN Lin, CHEN Zhiguo, LU Ming, LI Yingjun
CLC Number:
Committee of Experts on Medical Animal Experiments, Chinese Research Hospital Association,Committee of Regenerative Medicine Branch, Chinese Medicinal Biotech Association,HAN Fabin,et al. Guidelines for Selecting Preclinical Animal Models for Drugs and Stem Cell Therapies for Parkinson Disease (2026 Edition)[J]. Laboratory Animal and Comparative Medicine, 2026, 46(2): 153-177. DOI: 10.12300/j.issn.1674-5817.2025.073.
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URL: https://www.slarc.org.cn/dwyx/EN/10.12300/j.issn.1674-5817.2025.073
Figure 1 The projection pathway of striatal dopaminergic neurons in the direct and indirect pathways of the basal ganglia
分类 Classification | 症状 Symptom | 出现阶段 Stages of emergence | 临床表现 Clinical manifestation |
|---|---|---|---|
运动症状 Motor symptoms | 运动迟缓 | PD早期 | 自发运动普遍缓慢,手臂摆动、面部表情和手势减少,床上翻身困难,声音低沉;自主重复运动的速度和幅度逐渐降低,包括手指敲击、握力、旋前-旋后运动、脚趾敲击和足跟踩踏 |
| 肌强直 | PD早期 | 肌肉僵硬 | |
| 震颤 | PD早期 | 静止性震颤常发生于四肢、嘴唇和下颌,很少发生在头部。在以目标为导向的随意运动中,震颤幅度减少或消失;检查手部震颤时,患者处于坐位,双手放松,双臂支撑在大腿部 | |
| 步态改变 | PD早期 | 手臂摆动幅度减小,拖着一条腿,走路时姿势微弯 | |
| 姿势改变 | PD后期 | 站立时,躯干向前弯曲,双臂外展,肘部弯曲 | |
| 冻结步态 | PD后期 | 在行走开始、行走期间、转弯或接近狭窄空间时,突然或短暂地无法进行有效向前迈步 | |
| 平衡运动 | PD后期 | 站立和行走时身体不稳,容易跌倒 | |
| 构音障碍和吞咽困难 | PD后期 | 语言障碍,进食困难 | |
非运动症状 Non-motor symptoms | 嗅觉减退 | PD早期 | 多达70%患者表现为嗅觉丧失 |
| 睡眠障碍 | PD早期 | 快速眼动睡眠行为障碍,失眠,周期性肢体运动,静坐不能,白天嗜睡等 | |
| 精神科特征 | PD早期 | 明显的冷漠、焦虑、抑郁 | |
| 自主神经功能障碍 | PD早期 | 便秘,胃排空延迟,尿急或尿失禁,勃起功能障碍,直立性低血压,怕热 | |
| 轻度认知障碍 | PD早期 | 注意力和认知能力轻度下降 | |
| 疼痛和躯体感觉障碍 | PD早期 | 疼痛,感觉异常和烧灼感 | |
| 痴呆 | PD后期 | 约30%患者会出现痴呆的症状,该症状的发病率随着PD病程的发展而增加 |
Table 1 Motor and non-motor symptoms in early and late stages of Parkinson disease(PD)
分类 Classification | 症状 Symptom | 出现阶段 Stages of emergence | 临床表现 Clinical manifestation |
|---|---|---|---|
运动症状 Motor symptoms | 运动迟缓 | PD早期 | 自发运动普遍缓慢,手臂摆动、面部表情和手势减少,床上翻身困难,声音低沉;自主重复运动的速度和幅度逐渐降低,包括手指敲击、握力、旋前-旋后运动、脚趾敲击和足跟踩踏 |
| 肌强直 | PD早期 | 肌肉僵硬 | |
| 震颤 | PD早期 | 静止性震颤常发生于四肢、嘴唇和下颌,很少发生在头部。在以目标为导向的随意运动中,震颤幅度减少或消失;检查手部震颤时,患者处于坐位,双手放松,双臂支撑在大腿部 | |
| 步态改变 | PD早期 | 手臂摆动幅度减小,拖着一条腿,走路时姿势微弯 | |
| 姿势改变 | PD后期 | 站立时,躯干向前弯曲,双臂外展,肘部弯曲 | |
| 冻结步态 | PD后期 | 在行走开始、行走期间、转弯或接近狭窄空间时,突然或短暂地无法进行有效向前迈步 | |
| 平衡运动 | PD后期 | 站立和行走时身体不稳,容易跌倒 | |
| 构音障碍和吞咽困难 | PD后期 | 语言障碍,进食困难 | |
非运动症状 Non-motor symptoms | 嗅觉减退 | PD早期 | 多达70%患者表现为嗅觉丧失 |
| 睡眠障碍 | PD早期 | 快速眼动睡眠行为障碍,失眠,周期性肢体运动,静坐不能,白天嗜睡等 | |
| 精神科特征 | PD早期 | 明显的冷漠、焦虑、抑郁 | |
| 自主神经功能障碍 | PD早期 | 便秘,胃排空延迟,尿急或尿失禁,勃起功能障碍,直立性低血压,怕热 | |
| 轻度认知障碍 | PD早期 | 注意力和认知能力轻度下降 | |
| 疼痛和躯体感觉障碍 | PD早期 | 疼痛,感觉异常和烧灼感 | |
| 痴呆 | PD后期 | 约30%患者会出现痴呆的症状,该症状的发病率随着PD病程的发展而增加 |
α突触核蛋白基因 α-synuclein | 启动子 Promoter | 品种品系 Breed and strain | 多巴胺能神经元的损失率 Loss rate of dopaminergic neurons | α突触核蛋白的病理表型 Pathological phenotype of α-synuclein | 运动表型 Motor phenotype | 非运动表型 Non-motor phenotype |
|---|---|---|---|---|---|---|
| Gene fragments(1~130)[ | Thy-1 | C57BL/6J小鼠 | 约50% | 异常聚集 | 自发运动减少 | NA |
| A30P+A53T[ | Thy-1 | C57BL/6J小鼠 | 约50% | 包涵体 | 自发运动减少 | NA |
| A53T[ | PrP | C57BL/6J小鼠 | 约40% | 异常聚集 | 自发运动和在棒时间减少、步幅缩短 | NA |
| Wild type(SNCA-OVX line)[ | PrP | C57BL/6J×B6小鼠 | 约30% | 异常聚集 | 在棒时间减少,前爪步幅缩短 | 粪便重量增加 |
| Wild type[ | PrP | SD大鼠 | 约40% | 包涵体 | 自发活动和直立活动减少 | 嗅觉障碍 |
Table 2 Characteristics of transgenic mouse PD models with different α-synuclein
α突触核蛋白基因 α-synuclein | 启动子 Promoter | 品种品系 Breed and strain | 多巴胺能神经元的损失率 Loss rate of dopaminergic neurons | α突触核蛋白的病理表型 Pathological phenotype of α-synuclein | 运动表型 Motor phenotype | 非运动表型 Non-motor phenotype |
|---|---|---|---|---|---|---|
| Gene fragments(1~130)[ | Thy-1 | C57BL/6J小鼠 | 约50% | 异常聚集 | 自发运动减少 | NA |
| A30P+A53T[ | Thy-1 | C57BL/6J小鼠 | 约50% | 包涵体 | 自发运动减少 | NA |
| A53T[ | PrP | C57BL/6J小鼠 | 约40% | 异常聚集 | 自发运动和在棒时间减少、步幅缩短 | NA |
| Wild type(SNCA-OVX line)[ | PrP | C57BL/6J×B6小鼠 | 约30% | 异常聚集 | 在棒时间减少,前爪步幅缩短 | 粪便重量增加 |
| Wild type[ | PrP | SD大鼠 | 约40% | 包涵体 | 自发活动和直立活动减少 | 嗅觉障碍 |
模型类型 Model type | 建模成功时间 Time to successful model establishment | 损伤部位 Site of injury | 路易体 Lewy body | 成模检测时间 Detection time | 运动行为测试方法 Motor behavior testing method | 可重复性 Repeatability | 应用范围 Scope of application |
|---|---|---|---|---|---|---|---|
6-OHDA大鼠PD模型 6-OHDA rat PD model | 给药后1~3周内模型稳定 | 黑质致密部和纹状体 | 无 | 2~4周 | 旷场,转圈,转棒,步态运动明显减少 | 高(旋转行为与神经元损伤程度高度一致,成功率>90%) | DBS、药物、干细胞治疗干预 |
MPTP小鼠PD模型 MPTP mouse PD model | 给药后1~2周内模型稳定 | 黑质致密部和纹状体 | 无 | 2~4周 | 旷场,转棒,爬杆,步态运动明显减少 | 中(行为学测试结果可能存在个体差异) | DBS、药物、干细胞治疗干预 |
SNCA转基因大鼠PD模型 SNCA transgenic rat PD model | 3个月以上 | 根据转基因类型而定,可影响多个脑区 | 有 | 出生后数周至数月 | 旷场,转棒,步态运动减少 | 高(转基因技术可重复性强) | 基因治疗、药物干预 |
Parkin基因敲除小鼠PD模型 Parkin gene knockout mouse PD model | 3个月以上 | 根据转基因类型而定,可能影响多个脑区 | 无 | 出生后数周 | 旷场,爬杆,步态运动减少 | 高(转基因技术可重复性强) | 基因治疗、药物干预 |
Table 3 Comparison of characteristics of several commonly used rat and mouse models of Parkinson disease
模型类型 Model type | 建模成功时间 Time to successful model establishment | 损伤部位 Site of injury | 路易体 Lewy body | 成模检测时间 Detection time | 运动行为测试方法 Motor behavior testing method | 可重复性 Repeatability | 应用范围 Scope of application |
|---|---|---|---|---|---|---|---|
6-OHDA大鼠PD模型 6-OHDA rat PD model | 给药后1~3周内模型稳定 | 黑质致密部和纹状体 | 无 | 2~4周 | 旷场,转圈,转棒,步态运动明显减少 | 高(旋转行为与神经元损伤程度高度一致,成功率>90%) | DBS、药物、干细胞治疗干预 |
MPTP小鼠PD模型 MPTP mouse PD model | 给药后1~2周内模型稳定 | 黑质致密部和纹状体 | 无 | 2~4周 | 旷场,转棒,爬杆,步态运动明显减少 | 中(行为学测试结果可能存在个体差异) | DBS、药物、干细胞治疗干预 |
SNCA转基因大鼠PD模型 SNCA transgenic rat PD model | 3个月以上 | 根据转基因类型而定,可影响多个脑区 | 有 | 出生后数周至数月 | 旷场,转棒,步态运动减少 | 高(转基因技术可重复性强) | 基因治疗、药物干预 |
Parkin基因敲除小鼠PD模型 Parkin gene knockout mouse PD model | 3个月以上 | 根据转基因类型而定,可能影响多个脑区 | 无 | 出生后数周 | 旷场,爬杆,步态运动减少 | 高(转基因技术可重复性强) | 基因治疗、药物干预 |
特性 Characteristic | 猕猴 Macaque | 食蟹猴 Cynomolgus monkey | 狨猴 Marmoset |
|---|---|---|---|
MPTP敏感性(ED50值) MPTP sensitivity (ED50 value) | 猕猴对MPTP的敏感性存在个体差异。常用肌内注射MPTP的剂量从0.2 mg/kg开始,逐渐增加至0.5 mg/kg | 食蟹猴对MPTP的敏感性存在个体差异,且中老年食蟹猴对MPTP的敏感性更高。颈内动脉注射2~3 mg MPTP后辅以静脉注射(≤0.4 mg/kg) | 狨猴对MPTP的敏感性相对较低,通常需要更高的剂量(如每周0.5 mg/kg,连续5周)才能诱导出PD症状 |
行为学表型差异 Behavioral phenotype differences | 会出现静止性震颤、姿势/意向性震颤、运动迟缓、步态不稳、面部表情减少、姿势僵硬等典型症状,还可能伴有嗜睡、打哈欠、便秘、生活自理能力下降、发声减少等非典型症状 | 会出现明显的PD症状,如运动迟缓、震颤等,且症状的严重程度和进展速度因个体而异 | 会出现运动迟缓、震颤等症状,但症状的严重程度相对较低 |
成本评估 Cost assessment | 猕猴体型较大,饲养成本较高,且该动物对MPTP的敏感性存在个体差异,建模过程可能需要更多的时间和精力来调整给药方案 | 食蟹猴体型相对较小,饲养成本略低于猕猴,但其对MPTP的敏感性存在个体差异,建模过程中需要根据个体情况调整给药方案 | 狨猴体型最小,饲养成本相对较低,但需要更高的剂量才能诱导出症状,可能会增加药物成本 |
Table 4 Main characteristics of Parkinson disease models in macaques, cynomolgus monkeys, and marmosets
特性 Characteristic | 猕猴 Macaque | 食蟹猴 Cynomolgus monkey | 狨猴 Marmoset |
|---|---|---|---|
MPTP敏感性(ED50值) MPTP sensitivity (ED50 value) | 猕猴对MPTP的敏感性存在个体差异。常用肌内注射MPTP的剂量从0.2 mg/kg开始,逐渐增加至0.5 mg/kg | 食蟹猴对MPTP的敏感性存在个体差异,且中老年食蟹猴对MPTP的敏感性更高。颈内动脉注射2~3 mg MPTP后辅以静脉注射(≤0.4 mg/kg) | 狨猴对MPTP的敏感性相对较低,通常需要更高的剂量(如每周0.5 mg/kg,连续5周)才能诱导出PD症状 |
行为学表型差异 Behavioral phenotype differences | 会出现静止性震颤、姿势/意向性震颤、运动迟缓、步态不稳、面部表情减少、姿势僵硬等典型症状,还可能伴有嗜睡、打哈欠、便秘、生活自理能力下降、发声减少等非典型症状 | 会出现明显的PD症状,如运动迟缓、震颤等,且症状的严重程度和进展速度因个体而异 | 会出现运动迟缓、震颤等症状,但症状的严重程度相对较低 |
成本评估 Cost assessment | 猕猴体型较大,饲养成本较高,且该动物对MPTP的敏感性存在个体差异,建模过程可能需要更多的时间和精力来调整给药方案 | 食蟹猴体型相对较小,饲养成本略低于猕猴,但其对MPTP的敏感性存在个体差异,建模过程中需要根据个体情况调整给药方案 | 狨猴体型最小,饲养成本相对较低,但需要更高的剂量才能诱导出症状,可能会增加药物成本 |
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