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长期使用大麻二酚对雌性阿尔茨海默病小鼠模型学习能力和焦虑情绪的影响

Effect of long-term cannabidiol on learning and anxiety in a female Alzheimer's disease mouse model.

作者信息

Chesworth Rose, Cheng David, Staub Chloe, Karl Tim

机构信息

School of Medicine, Western Sydney University, Campbelltown, NSW, Australia.

Neuroscience Research Australia, Randwick, NSW, Australia.

出版信息

Front Pharmacol. 2022 Sep 27;13:931384. doi: 10.3389/fphar.2022.931384. eCollection 2022.

DOI:10.3389/fphar.2022.931384
PMID:36238565
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9551202/
Abstract

Cannabidiol is a promising potential therapeutic for neurodegenerative diseases, including Alzheimer's disease (AD). Our laboratory has shown that oral CBD treatment prevents cognitive impairment in a male genetic mouse model of AD, the hemizygous () mouse. However, as sex differences are evident in clinical populations and in AD mouse models, we tested the preventive potential of CBD therapy in female mice. In this study, 2.5-month-old female wildtype-like (WT) and mice were fed 20 mg/kg CBD or a vehicle gel pellets daily for 8 months and tested at 10.5 months in behavioural paradigms relevant to cognition (fear conditioning, FC; cheeseboard, CB; and novel object recognition test, NORT) and anxiety-like behaviours (elevated plus maze, EPM). In the CB, CBD reduced latencies to find a food reward in mice, compared to vehicle-treated controls, and this treatment effect was not evident in WT mice. In addition, CBD also increased speed early in the acquisition of the CB task in mice. In the EPM, CBD increased locomotion in mice but not in WT mice, with no effects of CBD on anxiety-like behaviour. CBD had limited effects on the expression of fear memory. These results indicate preventive CBD treatment can have a moderate spatial learning-enhancing effect in a female amyloid-β-based AD mouse model. This suggests CBD may have some preventive therapeutic potential in female familial AD patients.

摘要

大麻二酚是一种有前景的神经退行性疾病潜在治疗药物,包括阿尔茨海默病(AD)。我们实验室已表明,口服大麻二酚治疗可预防AD雄性基因小鼠模型——半合子()小鼠的认知障碍。然而,由于临床人群和AD小鼠模型中存在明显的性别差异,我们测试了大麻二酚疗法对雌性小鼠的预防潜力。在本研究中,给2.5月龄的雌性野生型样(WT)和小鼠每日喂食20mg/kg大麻二酚或载体凝胶颗粒,持续8个月,并在10.5月龄时在与认知相关的行为范式(恐惧条件反射,FC;棋盘,CB;和新物体识别测试,NORT)以及焦虑样行为(高架十字迷宫,EPM)中进行测试。在CB中,与载体处理的对照相比,大麻二酚缩短了小鼠找到食物奖励的潜伏期,而这种治疗效果在WT小鼠中不明显。此外,大麻二酚还提高了小鼠在CB任务获取早期的速度。在EPM中,大麻二酚增加了小鼠的运动,但对WT小鼠没有影响,且大麻二酚对焦虑样行为没有影响。大麻二酚对恐惧记忆的表达影响有限。这些结果表明,预防性大麻二酚治疗在基于淀粉样β蛋白的雌性AD小鼠模型中可产生适度的空间学习增强作用。这表明大麻二酚可能对女性家族性AD患者具有一定的预防性治疗潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0747/9551202/ec349da7a561/fphar-13-931384-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0747/9551202/cbdd22a4edf9/fphar-13-931384-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0747/9551202/a156968a002a/fphar-13-931384-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0747/9551202/e8d8b19e9ebf/fphar-13-931384-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0747/9551202/ec349da7a561/fphar-13-931384-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0747/9551202/cbdd22a4edf9/fphar-13-931384-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0747/9551202/a156968a002a/fphar-13-931384-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0747/9551202/e8d8b19e9ebf/fphar-13-931384-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0747/9551202/ec349da7a561/fphar-13-931384-g004.jpg

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