阿尔茨海默病的预防和治疗:乐观的理由。

Vladimir Volloch, Bjorn Olsen, Sophia Rits
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引用次数: 5

摘要

阿尔茨海默病领域正在发生范式转变。到目前为止,对阿尔茨海默病(AD)的一种观点,即旧的范式,认为它是由β -淀粉样蛋白(Aβ)的过度生产和细胞外积累引发和驱动的;一种被认为在健康和疾病中仅由其大前体βAPP的蛋白水解而产生的肽。根据这一观点,在阿尔茨海默病中,与Aβ过量产生相关的神经退行性变很早就开始了,在整个生命周期中积累,并在生命后期表现出症状。在阿尔茨海默病中β β产生的βAPP蛋白水解/分泌途径的特殊框架内设计的许多药物在动物模型中治疗甚至逆转AD症状方面取得了惊人的成功。无一例外,它们都在人体临床试验中表现出同样惊人的失败。这一范例在预防和治疗阿尔茨海默病方面提供了一些乐观的理由。在这种情况下,该病在症状期被认为是不可治疗的;即使是前驱症状的病例也被认为太迟,无法治疗,因为a β引发的损害已经积累了几十年,大概从20岁出头开始,为了有效,这是治疗干预应该开始并持续一生的时候。新的范式并没有质疑β β在AD中的重要作用,但假设βAPP蛋白水解/分泌途径中产生的β -淀粉样蛋白在人类中引起AD并不比在非人类哺乳动物中引起AD多,这些哺乳动物与人类共享这一途径,随着年龄的增长积累Aβ,但不会发病。根据这一观点,阿尔茨海默病是由ad特异性的Aβ产生途径驱动的,独立于βAPP,在动物中不存在。在生命后期,它的激活通过积累发生,通过细胞摄取分泌的a β和神经元保留在βAPP蛋白水解途径中产生的部分β -淀粉样蛋白,从而触发线粒体功能障碍。与线粒体功能障碍相关的细胞应激,或者可能是由其引发的综合应激反应(ISR),激活了ad特异性的Aβ生成途径。在该研究中,每一个常规生产的βAPP mRNA分子都可能反复作为严重截断的βAPP C99片段mRNA的模板,βAPP C99片段是a β的直接前体,在非分泌途径中加工,显然以神经元特异性的方式进行。由此产生的神经元内保留的Aβ增强了线粒体功能障碍,这反过来又维持了βAPP mRNA扩增途径的活性。这些自我繁殖的Aβ过量生产/线粒体功能障碍相互反馈循环构成了驱动AD并最终引发神经元死亡的引擎。在这种情况下,预防性治疗可以在βAPP mRNA扩增开始前的任何时间开始。此外,有充分的理由相信,通过阻断扩增途径的药物,不仅可以预防疾病,而且可以在早期AD症状已经表现出来的情况下阻止和逆转疾病。因此,新范式引入了阿尔茨海默病的新理论。它解释了观察到的不一致,确定了明确的治疗靶点,为新一代概念上不同的AD模型提供了蓝图,并指定了mRNA扩增途径的报告基因的设计。最重要的是,它为疾病的预防和早期症状阶段的治疗提供了详细的指导和切实的希望。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Alzheimer's Disease Prevention and Treatment: Case for Optimism.
A paradigm shift is under way in the Alzheimer's field. A view of Alzheimer's disease, AD, prevailing until now, the old paradigm, maintains that it is initiated and driven by the overproduction and extracellular accumulation of beta-amyloid, Aβ; a peptide assumed to be derived, both in health and disease, solely by proteolysis of its large precursor, βAPP. In AD, according to this view, Aβ overproduction-associated neurodegeneration begins early, accumulates throughout the lifespan, and manifests symptomatically late in life. A number of drugs, designed within the framework of exceptionality of the βAPP proteolytic/secretory pathway in Aβ production in Alzheimer's disease, achieved spectacular successes in treatment, even the reversal, of AD symptoms in animal models. Without exception, they all exhibited equally spectacular failures in human clinical trials. This paradigm provides few causes for optimism with regard to prevention and treatment of AD. In its context, the disease is considered untreatable in the symptomatic phase; even prodromal cases are assumed too advanced for treatment because Aβ-triggered damages have been accumulating for preceding decades, presumably starting in the early twenties and, to be effective, this is when therapeutic intervention should commence and continue for life. The new paradigm does not dispute the seminal role of Aβ in AD but posits that beta-amyloid produced in the βAPP proteolytic/secretory pathway causes AD in humans no more than it does in non-human mammals that share this pathway with humans, accumulate Aβ as they age, but do not develop the disease. Alzheimer's disease, according to this outlook, is driven by the AD-specific pathway of Aβ production, independent of βAPP and absent in animals. Its activation, late in life, occurs through accumulation, via both cellular uptake of secreted Aβ and neuronal retention of a fraction of beta-amyloid produced in the βAPP proteolytic pathway, of intraneuronal Aβ, which triggers mitochondrial dysfunction. Cellular stresses associated with mitochondrial dysfunction, or, probably, the integrated stress response, ISR, elicited by it, activate an AD-specific Aβ production pathway. In it, every conventionally produced βAPP mRNA molecule potentially serves repeatedly as a template for production of severely 5'-truncated mRNA encoding C99 fragment of βAPP, the immediate precursor of Aβ that is processed in a non-secretory pathway, apparently in a neuron-specific manner. The resulting intraneuronally retained Aβ augments mitochondrial dysfunction, which, in turn, sustains the activity of the βAPP mRNA amplification pathway. These self-propagating Aβ overproduction/mitochondrial dysfunction mutual feedback cycles constitute the engine that drives AD and ultimately triggers neuronal death. In this paradigm, preventive treatment can be initiated any time prior to commencement of βAPP mRNA amplification. Moreover, there are good reasons to believe that with a drug blocking the amplification pathway, it would be possible not only to preempt the disease but also stop and reverse it even when early AD symptoms are already manifested. Thus, the new paradigm introduces a novel theory of Alzheimer's disease. It explains the observed discordances, determines defined therapeutic targets, provides blueprints for a new generation of conceptually distinct AD models and specifies design of a reporter for the mRNA amplification pathway. Most importantly, it offers detailed guidance and tangible hope for prevention of the disease and its treatment at the early symptomatic stages.
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