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神经炎症中的炎性小体、兴奋效应与抗氧化剂:NRLP3在阿尔茨海默病中的作用

Inflammasomes, hormesis, and antioxidants in neuroinflammation: Role of NRLP3 in Alzheimer disease.

作者信息

Pennisi Manuela, Crupi Rosalia, Di Paola Rosanna, Ontario Maria Laura, Bella Rita, Calabrese Edward J, Crea Roberto, Cuzzocrea Salvatore, Calabrese Vittorio

机构信息

Department of Biomedical and Biotechnological Sciences, School of Medicine, University of Catania, Catania, Italy.

Spinal Unit, Emergency Hospital "Cannizzaro,", Catania, Italy.

出版信息

J Neurosci Res. 2017 Jul;95(7):1360-1372. doi: 10.1002/jnr.23986. Epub 2016 Nov 8.

Abstract

Alzheimer disease (AD) is a progressive neurodegenerative disorder leading to cognitive decline, neuropsychiatric symptoms, disability, caregiver burden, and premature death. It represents the most prevalent cause of dementia, and its incidence rates exponentially increase with increasing age. The number of Americans living with AD is rapidly increasing. An estimated 5.4 million Americans of all ages have AD in 2016. One in nine people aged 65 and older has AD, and by midcentury, someone in the United States will develop the disease every 33 sec. It is now accepted that neuroinflammation is a common feature of neurological disease. Inflammasomes, which are a multiprotein complex part of the innate immune system, induce inflammation in response to various stimuli, such as pathogens and stress. Inflammasomes activate proinflammatory caspases, such as caspase-1, leading to the activation of the proinflammatory cytokines interleukin (IL)-1b, IL-18, and IL-33, which promote neuroinflammation and brain pathologies. The nucleotide-binding oligomerization domain-like receptor family, pyrin domain-containing-3 (NLRP3) inflammasome is the best characterized in neurodegenerative diseases, in particular AD. Recent research suggests that NLRP3 could possibly be used in targeted therapies to alleviate neuroinflammation. Modulation of endogenous cellular defense mechanisms may be an innovative approach to therapeutic intervention in AD and other disorders associated with neuroinflammation and neurodegeneration. Herein, we introduce the hormetic dose-response concept and present possible mechanisms and applications to neuroprotection. We summarize the mechanisms involved in activation of the NLRP3 inflammasome and its role in neuroinflammation. We also address and propose the potential therapeutic utility of the nutritional antioxidants sulforaphane and hydroxytyrosol against particular signs and symptoms of AD. © 2016 Wiley Periodicals, Inc.

摘要

阿尔茨海默病(AD)是一种进行性神经退行性疾病,可导致认知功能下降、神经精神症状、残疾、照料者负担加重以及过早死亡。它是痴呆症最常见的病因,其发病率随年龄增长呈指数级上升。美国患AD的人数正在迅速增加。2016年估计所有年龄段的美国有540万人患有AD。65岁及以上的人群中每九人就有一人患有AD,到本世纪中叶,美国每33秒就会有一人患上这种疾病。目前人们公认神经炎症是神经系统疾病的一个共同特征。炎性小体是先天免疫系统的一种多蛋白复合体,可响应各种刺激(如病原体和应激)诱导炎症反应。炎性小体激活促炎半胱天冬酶,如半胱天冬酶-1,导致促炎细胞因子白细胞介素(IL)-1β、IL-18和IL-33的激活,这些细胞因子会促进神经炎症和脑部病变。核苷酸结合寡聚化结构域样受体家族含pyrin结构域3(NLRP3)炎性小体在神经退行性疾病尤其是AD中研究得最为深入。最近的研究表明,NLRP3可能可用于靶向治疗以减轻神经炎症。调节内源性细胞防御机制可能是对AD及其他与神经炎症和神经退行性变相关疾病进行治疗干预的一种创新方法。在此,我们介绍 hormetic剂量反应概念,并阐述其对神经保护的可能机制及应用。我们总结了NLRP3炎性小体激活所涉及的机制及其在神经炎症中的作用。我们还探讨并提出了营养抗氧化剂萝卜硫素和羟基酪醇对AD特定体征和症状的潜在治疗作用。© 2016威利期刊公司

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