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美金刚通过CD1小鼠的焦虑样行为破坏运动协调。

Memantine Disrupts Motor Coordination through Anxiety-like Behavior in CD1 Mice.

作者信息

Shuvaev Anton N, Belozor Olga S, Mozhei Oleg I, Mileiko Aleksandra G, Mosina Ludmila D, Laletina Irina V, Mikhailov Ilia G, Fritsler Yana V, Shuvaev Andrey N, Teschemacher Anja G, Kasparov Sergey

机构信息

Research Institute of Molecular Medicine and Pathobiochemistry, Krasnoyarsk State Medical University Named after Prof. V.F. Voino-Yasenetsky, 660022 Krasnoyarsk, Russia.

Institute of Living Systems, Immanuel Kant Baltic Federal University, 236041 Kaliningrad, Russia.

出版信息

Brain Sci. 2022 Apr 13;12(4):495. doi: 10.3390/brainsci12040495.

Abstract

Memantine is an FDA approved drug for the treatment of Alzheimer's disease. It reduces neurodegeneration in the hippocampus and cerebral cortex through the inhibition of extrasynaptic NMDA receptors in patients and mouse models. Potentially, it could prevent neurodegeneration in other brain areas and caused by other diseases. We previously used memantine to prevent functional damage and to retain morphology of cerebellar neurons and Bergmann glia in an optogenetic mouse model of spinocerebellar ataxia type-1 (SCA1). However, before suggesting wider use of memantine in clinics, its side effects must be carefully evaluated. Blockers of NMDA receptors are controversial in terms of their effects on anxiety. Here, we investigated the effects of chronic application of memantine over 9 weeks to CD1 mice and examined rotarod performance and anxiety-related behaviors. Memantine-treated mice exhibited an inability to adapt to anxiety-causing conditions which strongly affected their rotarod performance. A tail suspension test revealed increased signs of behavioral despair. These data provide further insights into the potential deleterious effects of memantine which may result from the lack of adaptation to novel, stressful conditions. This effect of memantine may affect the results of tests used to assess motor performance and should be considered during clinical trials of memantine in patients.

摘要

美金刚是一种经美国食品药品监督管理局(FDA)批准用于治疗阿尔茨海默病的药物。在患者和小鼠模型中,它通过抑制突触外N-甲基-D-天冬氨酸(NMDA)受体来减少海马体和大脑皮质中的神经退行性变。它有可能预防其他脑区由其他疾病引起的神经退行性变。我们之前在1型脊髓小脑共济失调(SCA1)的光遗传学小鼠模型中使用美金刚来预防功能损伤并维持小脑神经元和伯格曼胶质细胞的形态。然而,在建议在临床上更广泛地使用美金刚之前,必须仔细评估其副作用。NMDA受体阻滞剂对焦虑的影响存在争议。在此,我们研究了对CD1小鼠长期应用美金刚9周的影响,并检测了转棒试验表现和焦虑相关行为。接受美金刚治疗的小鼠表现出无法适应引起焦虑的条件,这严重影响了它们的转棒试验表现。悬尾试验显示行为绝望的迹象增加。这些数据进一步揭示了美金刚可能存在的有害影响,这可能是由于缺乏对新的应激条件的适应所致。美金刚的这种作用可能会影响用于评估运动表现的测试结果,在美金刚治疗患者的临床试验中应予以考虑。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6816/9027563/cdcb09869d2f/brainsci-12-00495-g001.jpg

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