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阿尔茨海默病及其他神经退行性疾病认知缺陷的药物治疗:利用传统工具和既定图谱探索新领域。

Pharmaceutical treatment for cognitive deficits in Alzheimer's disease and other neurodegenerative conditions: exploring new territory using traditional tools and established maps.

作者信息

Bartus Raymond T, Dean Reginald L

机构信息

Ceregene, Inc., 9381 Judicial Dr., Suite 130, San Diego, CA 92121, USA.

出版信息

Psychopharmacology (Berl). 2009 Jan;202(1-3):15-36. doi: 10.1007/s00213-008-1365-7. Epub 2008 Nov 15.

Abstract

RATIONALE

Over 30 years ago, we began to develop a nonhuman primate model to study cognitive deficits of age-related neurodegenerative diseases and their neuroanatomical-neurochemical underpinnings for purposes of translating this work toward first pharmacotherapies. This effort produced several notable findings that eventually received consensus support, which we have been asked to review.

OBJECTIVES

A discussion of these findings, in the context of issues and obstacles confronted and principles applied, might facilitate the development of even more effective models and treatments, not only for Alzheimer's disease (AD) but for many other disorders involving cognitive deficits.

RESULTS

Collectively, our research provided first evidence of the following: aged primates can be used as 'models' for human age-related neurodegenerative diseases; key cognitive deficits in early AD share important conceptual similarities to deficits in both aged monkeys as well as non-demented humans (e.g., age-associated memory impairment and mild cognitive impairment); pharmacological intervention can reduce age-related cognitive impairments in animals that are conceptually similar to those seen in human diseases, including AD; cholinergics would likely be the first approved therapeutics for AD; and that many other classes of drugs would not likely succeed.

CONCLUSIONS

Despite the early promise shown by behavioral/functional approaches to develop treatment strategies, the dramatic shift in focus away from behavioral outcomes in animal neurodegenerative research that began 20 years ago has compromised further progress and continues to impede our ability to understand how these diseases impair human cognition and what pathways might lead to effective therapies. Principles applied successfully in the past should provide guidance for facilitating efforts in the future.

摘要

原理

30多年前,我们开始开发一种非人类灵长类动物模型,以研究与年龄相关的神经退行性疾病的认知缺陷及其神经解剖学 - 神经化学基础,目的是将这项工作转化为首批药物治疗方法。这项努力产生了几个显著的发现,最终得到了共识支持,我们被要求对此进行回顾。

目标

在面对的问题和障碍以及应用的原则的背景下讨论这些发现,可能会促进更有效模型和治疗方法的开发,不仅适用于阿尔茨海默病(AD),也适用于许多其他涉及认知缺陷的疾病。

结果

总体而言,我们的研究首次提供了以下证据:老年灵长类动物可作为人类与年龄相关的神经退行性疾病的“模型”;早期AD的关键认知缺陷与老年猴子以及未患痴呆症的人类的缺陷在重要概念上有相似之处(例如,年龄相关记忆损害和轻度认知障碍);药物干预可以减少动物中与年龄相关的认知障碍,这些障碍在概念上与人类疾病(包括AD)中所见的相似;胆碱能药物可能是首批被批准用于AD的治疗药物;而且许多其他类别的药物可能不会成功。

结论

尽管行为/功能方法在制定治疗策略方面早期显示出前景,但20年前开始的动物神经退行性研究中从行为结果上的重点大幅转移已经损害了进一步的进展,并继续阻碍我们理解这些疾病如何损害人类认知以及哪些途径可能导致有效治疗的能力。过去成功应用的原则应为未来的努力提供指导。

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