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小分子转化生长因子-β模拟物作为潜在的神经保护因子。

Small molecule tgf-beta mimetics as potential neuroprotective factors.

作者信息

Zhang Hui, Zou Kun, Tesseur Ina, Wyss-Coray Tony

机构信息

Department of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, CA 94305, USA.

出版信息

Curr Alzheimer Res. 2005 Apr;2(2):183-6. doi: 10.2174/1567205053585756.

Abstract

Neurodegenerative and dementing illnesses are becoming an increasing social and economical burden as the number of older people continues to grow in industrialized countries. Current knowledge of the processes leading to these diseases is still limited, and very few effective treatments are available. Because neurodegeneration is associated with an activation of injury and innate immune responses in the brain, drugs that could mimic the beneficial aspects of this response are potential therapeutic candidates. The cytokine transforming growth factor (TGF)-beta1 is an organizer of the brain's response to injury and is known to be neuroprotective. Previous studies from our lab also showed that TGF-beta1 can reduce accumulation of beta-amyloid peptide (Abeta), which appears to be central to Alzheimer's disease (AD) pathogenesis, and we therefore initiated a search for small molecule chemical compounds that could mimic this effect. We report here the identification of several such TGF-beta mimetics detected in an in vitro screen of a library with 5000 chemically diverse compounds. If active in vivo, these mimetics could be developed into candidates for the treatment of neurodegeneration.

摘要

随着工业化国家老年人数量持续增长,神经退行性疾病和痴呆症正成为日益沉重的社会和经济负担。目前对于导致这些疾病的过程的了解仍然有限,并且几乎没有有效的治疗方法。由于神经退行性变与大脑中损伤和固有免疫反应的激活有关,能够模拟这种反应有益方面的药物是潜在的治疗候选物。细胞因子转化生长因子(TGF)-β1是大脑对损伤反应的组织者,并且已知具有神经保护作用。我们实验室之前的研究还表明,TGF-β1可以减少β-淀粉样肽(Aβ)的积累,而Aβ似乎是阿尔茨海默病(AD)发病机制的核心,因此我们开始寻找能够模拟这种作用的小分子化合物。我们在此报告在对一个包含5000种化学结构不同化合物的文库进行体外筛选时发现了几种这样的TGF-β模拟物。如果这些模拟物在体内具有活性,它们可能会被开发成为治疗神经退行性变的候选药物。

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