Amisulpride Decreases Tau Protein Hyperphosphorylation in the Brain of OXYS Rats.

IF 1.8 4区 医学 Q3 CLINICAL NEUROLOGY
Camilla A Molobekova, Elena M Kondaurova, Tatiana V Ilchibaeva, Alexander Ya Rodnyy, Natalia A Stefanova, Nataliya G Kolosova, Vladimir S Naumenko
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引用次数: 0

Abstract

Aim: In this study, OXYS rats of three ages (1, 3, and 6 months), a proven model of Alzheimer's disease (AD), at various stages of disease progression were used to thoroughly study the effects of amisulpride on behavior and tau protein phosphorylation.

Background: With the growing number of patients with AD, the problem of finding a cure is very acute. Neurodegeneration in AD has various causes, one of which is hyperphosphorylation of tau protein.

Objective: This study aimed to investigate whether amisulpride would affect pathological tau phosphorylation in AD.

Methods: We assessed the influence of chronic administration of amisulpride (3 weeks, 3 mg/kg per day, intraperitoneally)-a 5-HT7 receptor inverse agonist-on behavior and tau hyperphosphorylation in OXYS rats (at ages of 1, 3, and 6 months).

Results: Chronic administration of amisulpride dramatically decreased tau phosphorylation in the frontal cortex and hippocampus of 3-month-old OXYS rats. Additionally, in 1- and 3-month-old rats' hippocampi, amisulpride diminished the mRNA level of the Cdk5 gene encoding one of the main tau kinases involved in the 5-HT7 receptor-induced effect on tau phosphorylation.

Conclusion: Thus, We found that chronic administration of amisulpride could reduce pathological tau hyperphosphorylation while reducing anxiety. We propose amisulpride to have therapeutic potential against AD and that it can be the most effective in the early stages of the disease.

氨硫pride降低OXYS大鼠脑内Tau蛋白过度磷酸化。
目的:在本研究中,采用三龄(1、3和6个月)的OXYS大鼠(一种已证实的阿尔茨海默病(AD)模型),在疾病进展的不同阶段,深入研究氨硫pride对行为和tau蛋白磷酸化的影响。背景:随着AD患者数量的不断增加,寻找治疗方法的问题非常紧迫。阿尔茨海默病的神经退行性变有多种原因,其中之一是tau蛋白的过度磷酸化。目的:探讨氨硫pride对AD病理性tau蛋白磷酸化的影响。方法:我们评估了长期给药氨硫pride(3周,每天3mg /kg,腹腔注射)-一种5-HT7受体逆激动剂对OXYS大鼠(1、3和6个月大)行为和tau过度磷酸化的影响。结果:长期服用氨硫pride可显著降低3月龄OXYS大鼠额叶皮质和海马的tau磷酸化。此外,在1个月和3个月大鼠的海马中,氨硫pride降低了Cdk5基因的mRNA水平,Cdk5基因编码一种主要的tau激酶,参与5-HT7受体诱导的tau磷酸化作用。结论:因此,我们发现长期服用氨硫pride可以减少病理性tau过度磷酸化,同时减少焦虑。我们认为氨硫pride具有治疗AD的潜力,并且在疾病的早期阶段是最有效的。
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来源期刊
Current Alzheimer research
Current Alzheimer research 医学-神经科学
CiteScore
4.00
自引率
4.80%
发文量
64
审稿时长
4-8 weeks
期刊介绍: Current Alzheimer Research publishes peer-reviewed frontier review, research, drug clinical trial studies and letter articles on all areas of Alzheimer’s disease. This multidisciplinary journal will help in understanding the neurobiology, genetics, pathogenesis, and treatment strategies of Alzheimer’s disease. The journal publishes objective reviews written by experts and leaders actively engaged in research using cellular, molecular, and animal models. The journal also covers original articles on recent research in fast emerging areas of molecular diagnostics, brain imaging, drug development and discovery, and clinical aspects of Alzheimer’s disease. Manuscripts are encouraged that relate to the synergistic mechanism of Alzheimer''s disease with other dementia and neurodegenerative disorders. Book reviews, meeting reports and letters-to-the-editor are also published. The journal is essential reading for researchers, educators and physicians with interest in age-related dementia and Alzheimer’s disease. Current Alzheimer Research provides a comprehensive ''bird''s-eye view'' of the current state of Alzheimer''s research for neuroscientists, clinicians, health science planners, granting, caregivers and families of this devastating disease.
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