氯唑沙宗和叶酸的组合能改善 SCA3-84Q 小鼠的识别记忆、焦虑和抑郁。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-08-06 DOI:10.1093/hmg/ddae079
Ksenia S Marinina, Ilya B Bezprozvanny, Polina A Egorova
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引用次数: 0

摘要

据报道,脊髓小脑共济失调 3 型(SCA3)又称马查多-约瑟夫病,是常染色体显性小脑共济失调(ADCA)中最常见的一种类型。SCA3 患者的运动协调能力会逐渐下降,并伴有其他疾病相关症状。此外,最近有研究报告称,SCA3 患者还表现出小脑认知情感综合征(CCAS)的症状。我们曾在SCA3小鼠模型中观察到CCAS的症状。特别是,SCA3-84Q小鼠患有焦虑症、识别记忆力下降,还表现出情绪低落和厌恶活动的症状。在此,我们研究了长期注射 SK 通道激活剂氯唑沙宗(CHZ)和叶酸(FA)对 SCA3-84Q 半杂合子转基因小鼠小脑普肯耶细胞(PC)发射和组织学、运动和认知功能以及情绪改变的影响。我们发现,CHZ和CHZ-FA组合对SCA3-84Q小鼠的纯小脑损伤(包括PC发射精确度、PC组织学和运动表现)具有相似的积极作用。然而,只有CHZ-FA组合(而非CHZ)能显著改善SCA3-84Q小鼠的焦虑和抑郁症状,并明显改善其识别记忆。我们的研究结果表明,共济失调和非运动症状的联合治疗是ADCA的复合治疗所必需的。
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A combination of chlorzoxazone and folic acid improves recognition memory, anxiety and depression in SCA3-84Q mice.

Spinocerebellar ataxia type 3 (SCA3), also known as Machado-Joseph disease, is reported to be the most common type of autosomal dominant cerebellar ataxia (ADCA). SCA3 patients suffer from a progressive decline in motor coordination and other disease-associated symptoms. Moreover, recent studies have reported that SCA3 patients also exhibit symptoms of cerebellar cognitive affective syndrome (CCAS). We previously observed signs of CCAS in mouse model of SCA3. Particularly, SCA3-84Q mice suffer from anxiety, recognition memory decline, and also exhibit signs of low mood and aversion to activity. Here we studied the effect of long-term injections of SK channels activator chlorzoxazone (CHZ) together and separately with the folic acid (FA) on the cerebellar Purkinje cell (PC) firing and histology, and also on the motor and cognitive functions as well as mood alterations in SCA3-84Q hemizygous transgenic mice. We realized that both CHZ and CHZ-FA combination had similar positive effect on pure cerebellum impairments including PC firing precision, PC histology, and motor performance in SCA3-84Q mice. However, only the CHZ-FA combination, but not CHZ, had significantly ameliorated the signs of anxiety and depression, and also noticeably improved recognition memory in SCA3-84Q mice. Our results suggest that the combination therapy for both ataxia and non-motor symptoms is required for the complex treatment of ADCA.

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4.30%
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567
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