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辛伐他汀可抑制阿尔茨海默病小鼠模型中海马细胞的凋亡。

Simvastatin inhibits the apoptosis of hippocampal cells in a mouse model of Alzheimer's disease.

作者信息

Hu Xiaoqin, Song Chengwei, Fang Ming, Li Chengyan

机构信息

Department of Neurology, Remnin Hospital of Wuhan University, Wuhan, Hubei 430060, P.R. China.

Department of Neurology, The First Hospital of Yichang, The Gorges University College of Medicine, Yichang, Hubei 443000, P.R. China.

出版信息

Exp Ther Med. 2018 Feb;15(2):1795-1802. doi: 10.3892/etm.2017.5620. Epub 2017 Dec 12.

Abstract

Alzheimer's disease is associated with cognitive impairments that affect memory and executive functions. Simvastatin is a cholesterol-lowering statin drug that is used to control levels of cholesterol in the blood, particularly in cases of hypercholesterolemia, and may be used in the treatment of aneurysmal subarachnoid hemorrhage. Previous results have indicated that the apoptosis of hippocampal cells may serve a critical role in the progression of Alzheimer's disease. In the present study, it was determined whether Simvastatin inhibited the apoptosis of hippocampal cells and . The therapeutic effects of Simvastatin were evaluated in 24-month-old triple-transgenic Alzheimer's disease (3×Tg-AD) mice, and the efficacy of Simvastatin in attenuating memory and cognitive impairment was investigated. Levels of apoptosis-related gene expression in the hippocampus and hippocampal cells of experimental mice were also detected. In addition, neuron excitability was assessed in the functionally relevant brain regions in the hippocampus. The data indicated that Simvastatin significantly suppressed the apoptosis of hippocampal cells in 3×Tg-AD model mice compared with controls (P<0.01). Furthermore, treatment with Simvastatin improved the dementia status of 3×Tg-AD mice, as determined by a learning task in which mice exhibited significantly reduced attention impairment, impulsivity and compulsivity (P<0.01). In addition, results demonstrated that Simvastatin significantly inhibited hippocampal damage and significantly improved neuronal loss in hippocampal structures classically associated with attentional performance when compared with untreated mice (P<0.01). Thus, Simvastatin prevented cognitive impairment by decreasing hippocampal cell apoptosis and improving learning-memory ability. Simvastatin treatment also increased the expression of anti-apoptotic genes and decreased the expression pro-apoptotic genes (P<0.01), which may have been associated with improved motor attention and cognitive competence in 3×Tg-AD mice. Collectively, these preclinical data indicated that Simvastatin was efficient in attenuating memory lapse and hippocampal cell apoptosis in a 3×Tg-AD mouse model. Thus, Simvastatin may be useful in improving the clinical outcome of patients with Alzheimer's disease.

摘要

阿尔茨海默病与影响记忆和执行功能的认知障碍有关。辛伐他汀是一种降胆固醇的他汀类药物,用于控制血液中的胆固醇水平,尤其是在高胆固醇血症的情况下,也可用于治疗动脉瘤性蛛网膜下腔出血。先前的结果表明,海马细胞的凋亡可能在阿尔茨海默病的进展中起关键作用。在本研究中,确定了辛伐他汀是否抑制海马细胞的凋亡。在24月龄的三联转基因阿尔茨海默病(3×Tg-AD)小鼠中评估了辛伐他汀的治疗效果,并研究了辛伐他汀在减轻记忆和认知障碍方面的疗效。还检测了实验小鼠海马和海马细胞中凋亡相关基因的表达水平。此外,在海马功能相关的脑区评估了神经元兴奋性。数据表明,与对照组相比,辛伐他汀显著抑制了3×Tg-AD模型小鼠海马细胞的凋亡(P<0.01)。此外,通过一项学习任务确定,辛伐他汀治疗改善了3×Tg-AD小鼠的痴呆状态,在该任务中,小鼠表现出注意力障碍、冲动性和强迫性显著降低(P<0.01)。此外,结果表明,与未治疗的小鼠相比,辛伐他汀显著抑制了海马损伤,并显著改善了经典上与注意力表现相关的海马结构中的神经元丢失(P<0.01)。因此,辛伐他汀通过减少海马细胞凋亡和提高学习记忆能力预防了认知障碍。辛伐他汀治疗还增加了抗凋亡基因的表达,降低了促凋亡基因的表达(P<0.01),这可能与3×Tg-AD小鼠运动注意力和认知能力的改善有关。总的来说,这些临床前数据表明,辛伐他汀在减轻3×Tg-AD小鼠模型中的记忆衰退和海马细胞凋亡方面是有效的。因此,辛伐他汀可能有助于改善阿尔茨海默病患者的临床结局。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0e4/5776644/82cdc83d370e/etm-15-02-1795-g00.jpg

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