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中国临床药理学与治疗学 ›› 2024, Vol. 29 ›› Issue (6): 629-636.doi: 10.12092/j.issn.1009-2501.2024.06.004

• 基础研究 • 上一篇    下一篇

抗震止痉方对亚急性帕金森模型小鼠的病程进展干预研究

白雪纯1,2,陈硕1,李珊珊1,李庆林1   

  1. 1安徽中医药大学新安医学教育部重点实验室,合肥  230038,安徽;2安徽中医药大学药学院,合肥  230038,安徽

  • 收稿日期:2023-11-09 修回日期:2023-12-05 出版日期:2024-06-26 发布日期:2024-05-20
  • 通讯作者: 李庆林,教授,博士生导师,研究方向:中药及天然活性成分干预肿瘤及神经退行性疾病的分子机制研究。 E-mail: liqinlin@ahtcm.edu.com
  • 作者简介:白雪纯,硕士,研究方向:神经药理学方向研究。 E-mail: 1099265091@qq.com
  • 基金资助:
    特色皖药(黄精、凤丹、茯苓)综合利用与开发研究(GXXT-2020-025);2023年安徽省高校自然科学研究项目(2023AH050742);安徽中医药大学自然科学研究项目计划(2021zrzd05)

Intervention study on the progress of subacute Parkinson's disease in mice with Kangzhen Zhijing spasmodic decoction Ⅰ

BAI Xuechun1,2, CHEN Shuo1, LI Shanshan1, LI Qinglin1   

  1. 1Key Laboratory of Xin'an Medicine, Ministry of Education, Anhui University of Chinese Medicine, Hefei 230038, Anhui, Chin; 2School of Pharmacy, Anhui University of Chinese Medicine, Hefei 230038, Anhui, China 
  • Received:2023-11-09 Revised:2023-12-05 Online:2024-06-26 Published:2024-05-20

摘要:

目的:观察中药抗震止痉Ⅰ号方对帕金森模型小鼠病程进展的干预作用,并探讨其神经保护的潜在机制。方法:36只C57BL/6小鼠随机平均分为对照组、模型组、给药组、阳性药组。模型组、给药组及阳性药组采用1-甲基-4-苯基-1,2,3,6-四氢吡啶(1-METHYL-4-PHENYL-1,2,3,6-TETRAHYDROPYRIDINE,MPTP)(30 mg/kg)连续腹腔注射5 d,制备PD小鼠模型。对照组给与等量的生理盐水,给药组采用1.25、2.5、5 mg/kg的剂量灌胃中药抗震止痉Ⅰ号,阳性药组采用75 mg/kg美多芭灌胃给药。给药结束后第2天进行行为学检测各组小鼠的运动能力。采用免疫组织化学法检测酪氨酸羟化酶(TH)、淀粉样前体蛋白(APP)、α-突触核蛋白(α-syn)、溶质载体家族6成员11(SLC6A11)免疫阳性细胞情况;采用Western Blot方法考察各组小鼠TH、APP、α-syn、SLC6A11的蛋白表达情况。结果:抗震止痉Ⅰ号方可以明显改善模型组小鼠体质量减轻现象,缓解模型组小鼠旷场实验自主活动能力减退和爬杆实验及悬挂实验协调能力的下降;提高模型组小鼠脑中TH、SLC6A11的蛋白表达,降低APP、α-syn的蛋白表达。结论:抗震止痉Ⅰ号可以明显改善帕金森模型小鼠的行为学表现,并有效改善神经元递质的丢失。

关键词: 动物模型, 行为学, 帕金森, 神经保护, 神经退行性疾病

Abstract:

AIM: To observe the intervention effect of Chinese medicine Kangzhen Zhijing spasmodic decoction Ⅰ on the progression of Parkinson's disease in mice, and to explore the potential mechanism of neuroprotection. METHODS: Thirty-six C57BL/6 mice were randomly divided into control group, model group, drug group and positive drug group. In the model group, the drug administration group and the positive drug group,1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) (30 mg/kg) was injected intraperitoneally for 5 days to establish the mouse model. The control group was given the same amount of normal saline,the drug administration group was given 1.25 mg/kg, 2.5 mg/kg, 5 mg/kg dose of Chinese medicine Kangzhen Zhijing spasmodic Decoction Ⅰ by gavage, and the positive drug group was given 75 mg/kg Madopar by gavage. Behavioral tests were performed on the second day after the administration in each group. Immunopositive cells of Tyrosine hydroxylase (TH),Amyloid precursor protein (APP), α-synuclein (α-syn) and solute carrier family 6 member 11 (SLC6A11) were detected by immunohistochemistry. The protein expressions of TH, APP, α-syn and SLC6A11 in each group were detected by Western blot. RESULTS: It could significantly improve the weight loss of mice in the model group, alleviate the decline of autonomic activity in open field test and the decline of coordination ability in pole test and suspension test. In the reverse immunohistochemistry and Western Blot experiments, the expressions of TH and SLC6A11 in the brain of the Parkinson's model group were significantly decreased, and the expressions of APP and α-syn were significantly increased. CONCLUSION: Kangzhen Zhijing spasmodic decoction Ⅰ can significantly improve the behavioral performance of Parkinson's disease mice and effectively improve the reduction of neuronal transmitters.

Key words: animal model, behavioral science, Parkinson's disease, neuroprotection, neurodegenerative diseases

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