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
), CHEN Lin(
), CHEN Zhiguo(
), LU Ming(
), LI Yingjun(
)
Received:2025-05-15
Revised:2025-08-15
Online:2026-04-25
Published:2026-04-18
Contact:
HAN Fabin, CHEN Lin, CHEN Zhiguo, LU Ming, LI Yingjun
CLC Number:
HAN Fabin,CHEN Lin,CHEN Zhiguo,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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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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