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首页> 外文期刊>Journal of biological inorganic chemistry: JBIC: a publication of the Society of Biological Inorganic Chemistry >Metals in medicine: metal-related diseases-Peptide-based chelating drugs in diagnosis and treatment of Alzheimer disease
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Metals in medicine: metal-related diseases-Peptide-based chelating drugs in diagnosis and treatment of Alzheimer disease

机译:药物中的金属:与金属有关的疾病-肽基螯合剂在阿尔茨海默氏病的诊断和治疗中

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Alzheimer's disease (AD) is a devastating neuro-degenerative disorder characterized by the progressive and irreversible loss of memory followed by complete dementia. Despite the disease's high prevalence and great economic and social burden, an explicative aetiology or viable cure is still not available. Currently available therapeutics for AD only alleviate its symptoms [1]. TheAD-affected brain suffers from metal-ion homeostasis (metallostasis), resulting in redistribution of metals into inappropriate compartments. This metal disorder gives rise to the production of amyloid-β aggregates (SPs) and oxidative stress, which are two associated signs ofADpathology. To date, all clinical trials targeting amyloid β have failed; however, some clinical trials targeting metal interactions with amyloid b have all shown benefit for patients [2]. In addition, recent data indicate thatmetals play a role more upstream in the disease process than previously thought and might provide new targets for pharmacotherapy [3]. Consequently, targeting metals probably represents a tractable avenue for an AD-modifying therapy.
机译:阿尔茨海默氏病(AD)是一种破坏性神经退行性疾病,其特征在于进行性和不可逆的记忆力丧失,然后是完全性痴呆。尽管该病的高流行和巨大的经济和社会负担,但仍无法获得明确的病因学或可行的治疗方法。目前可用的AD疗法仅减轻其症状[1]。受AD影响的大脑患有金属离子稳态(金属稳态),导致金属重新分配到不适当的隔室中。这种金属异常会引起淀粉样β聚集体(SPs)的产生和氧化应激,这是AD病理学的两个相关征兆。迄今为止,所有针对β淀粉样蛋白的临床试验均失败。但是,一些针对金属与淀粉样蛋白b相互作用的临床试验均显示对患者有益[2]。此外,最新数据表明,金属在疾病过程中的上游作用比以前认为的要高,并且可能为药物治疗提供新的靶点[3]。因此,靶向金属可能代表了修饰AD的治疗方法。

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