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阿尔茨海默病:基础与治疗方面

Alzheimer's disease: fundamental and therapeutic aspects.

作者信息

Schorderet M

机构信息

Département de Pharmacologie, Centre Médical Universitaire, Genève, Switzerland.

出版信息

Experientia. 1995 Feb 15;51(2):99-105. doi: 10.1007/BF01929348.

Abstract

Alzheimer's disease is the most common type of progressive and debilitating dementia affecting aged people. In some early--as well as late--onset familial cases, a genetic linkage with chromosomes 14, 21 (early-onset) or 19 (late-onset) has been indicated. Furthermore, a direct or indirect role has been attributed to normal or structurally altered amyloid beta-protein (concentrated in senile plaques) and/or excessively phosphorylated tau protein (located in neurofibrillary tangles). Degeneration of cholinergic neurons and concomitant impairment of cortical and hippocampal neurotransmission lead to cognitive and memory deficits. Several compounds are being tested in attempts to prevent and/or cure Alzheimer's disease, including tacrine, which has very modest efficacy in a sub-group of patients, and new acetylcholinesterase inhibitors. Pilot experiments have also been launched using nerve growth factor (NGF) to prevent or stabilize the processes of cholinergic pathway degeneration. Alternatively, antioxidants, free radical scavengers and/or non steroidal anti-inflammatory agents may be screened as potential therapies for neurodegenerative diseases induced by multiple endogenous and/or exogenous factors. The recent use of transgenic mice, in parallel with other genetic, biochemical and neurobiological systems, in vivo and/or in vitro (cell cultures), should accelerate the discovery and development of specific drugs for the treatment of Alzheimer's disease.

摘要

阿尔茨海默病是影响老年人的最常见的进行性和致残性痴呆类型。在一些早发性和晚发性家族病例中,已表明与14号、21号染色体(早发性)或19号染色体(晚发性)存在基因连锁关系。此外,正常或结构改变的β-淀粉样蛋白(集中在老年斑中)和/或过度磷酸化的tau蛋白(位于神经原纤维缠结中)被认为具有直接或间接作用。胆碱能神经元的退化以及随之而来的皮质和海马神经传递受损导致认知和记忆缺陷。目前正在测试几种化合物以试图预防和/或治愈阿尔茨海默病,包括他克林(在一小部分患者中疗效甚微)以及新型乙酰胆碱酯酶抑制剂。还开展了使用神经生长因子(NGF)来预防或稳定胆碱能途径退化过程的初步实验。此外,抗氧化剂、自由基清除剂和/或非甾体抗炎药可能被筛选作为由多种内源性和/或外源性因素引起的神经退行性疾病的潜在治疗方法。最近使用转基因小鼠,以及其他遗传、生化和神经生物学系统,在体内和/或体外(细胞培养)进行研究,应能加速用于治疗阿尔茨海默病的特定药物的发现和开发。

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