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本文引用的文献

1
Midlife coffee and tea drinking and the risk of late-life dementia: a population-based CAIDE study.中年时期喝咖啡和茶与晚年患痴呆症的风险:一项基于人群的CAIDE研究。
J Alzheimers Dis. 2009;16(1):85-91. doi: 10.3233/JAD-2009-0920.
2
Involvement of cholesterol in the pathogenesis of Alzheimer's disease: role of statins.胆固醇在阿尔茨海默病发病机制中的作用:他汀类药物的角色。
Psychiatr Danub. 2008 Jun;20(2):162-7.
3
Potential therapeutic interest of adenosine A2A receptors in psychiatric disorders.腺苷A2A受体在精神疾病中的潜在治疗价值。
Curr Pharm Des. 2008;14(15):1512-24. doi: 10.2174/138161208784480090.
4
Silk polymer-based adenosine release: therapeutic potential for epilepsy.基于丝聚合物的腺苷释放:癫痫的治疗潜力
Biomaterials. 2008 Sep;29(26):3609-16. doi: 10.1016/j.biomaterials.2008.05.010. Epub 2008 Jun 2.
5
Caffeine prevents age-associated recognition memory decline and changes brain-derived neurotrophic factor and tirosine kinase receptor (TrkB) content in mice.咖啡因可预防与年龄相关的认知记忆衰退,并改变小鼠大脑源性神经营养因子和酪氨酸激酶受体(TrkB)的含量。
Neuroscience. 2008 Jun 2;153(4):1071-8. doi: 10.1016/j.neuroscience.2008.03.038. Epub 2008 Mar 22.
6
Neuroprotection by adenosine in the brain: From A(1) receptor activation to A (2A) receptor blockade.腺苷对大脑的神经保护作用:从 A(1)受体激活到 A (2A)受体阻断。
Purinergic Signal. 2005 Jun;1(2):111-34. doi: 10.1007/s11302-005-0649-1. Epub 2005 Mar 17.
7
Enhancement of long-term potentiation by brain-derived neurotrophic factor requires adenosine A2A receptor activation by endogenous adenosine.脑源性神经营养因子增强长期增强效应需要内源性腺苷激活腺苷A2A受体。
Neuropharmacology. 2008 May;54(6):924-33. doi: 10.1016/j.neuropharm.2008.01.011. Epub 2008 Feb 8.
8
Up-regulation of adenosine receptors in the frontal cortex in Alzheimer's disease.阿尔茨海默病患者额叶皮质中腺苷受体的上调。
Brain Pathol. 2008 Apr;18(2):211-9. doi: 10.1111/j.1750-3639.2007.00112.x. Epub 2008 Jan 29.
9
Adenosine receptor antagonists for cognitive dysfunction: a review of animal studies.用于认知功能障碍的腺苷受体拮抗剂:动物研究综述
Front Biosci. 2008 Jan 1;13:2614-32. doi: 10.2741/2870.
10
Adenosine as a neuromodulator in neurological diseases.腺苷作为神经疾病中的一种神经调质
Curr Opin Pharmacol. 2008 Feb;8(1):2-7. doi: 10.1016/j.coph.2007.09.002. Epub 2007 Oct 17.

腺苷在阿尔茨海默病中的作用。

The role of adenosine in Alzheimer's disease.

机构信息

Legacy Research, R.S Dow Neurobiology Laboratories, 1225 NE 2nd Avenue, Portland OR 97232, USA.

出版信息

Curr Neuropharmacol. 2009 Sep;7(3):207-16. doi: 10.2174/157015909789152119.

DOI:10.2174/157015909789152119
PMID:20190962
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2769004/
Abstract

Alzheimer's disease (AD) is a neurodegenerative disorder of the central nervous system manifested by cognitive and memory deterioration, a variety of neuropsychiatric symptoms, behavioral disturbances, and progressive impairment of daily life activities. Current pharmacotherapies are restricted to symptomatic interventions but do not prevent progressive neuronal degeneration. Therefore, new therapeutic strategies are needed to intervene with these progressive pathological processes. In the past several years adenosine, a ubiquitously released purine ribonucleoside, has become important for its neuromodulating capability and its emerging positive experimental effects in neurodegenerative diseases. Recent research suggests that adenosine receptors play important roles in the modulation of cognitive function. The present paper attempts to review published reports and data from different studies showing the evidence of a relationship between adenosinergic function and AD-related cognitive deficits. Epidemiological studies have found an association between coffee (a nonselective adenosine receptor antagonist) consumption and improved cognitive function in AD patients and in the elderly. Long-term administration of caffeine in transgenic animal models showed a reduced amyloid burden in brain with better cognitive performance. Antagonists of adenosine A2A receptors mimic these beneficial effects of caffeine on cognitive function. Neuronal cell cultures with amyloid beta in the presence of an A2A receptor antagonist completely prevented amyloid beta-induced neurotoxicity. These findings suggest that the adenosinergic system constitutes a new therapeutic target for AD, and caffeine and A2A receptor antagonists may have promise to manage cognitive dysfunction in AD.

摘要

阿尔茨海默病(AD)是一种中枢神经系统的神经退行性疾病,表现为认知和记忆恶化、各种神经精神症状、行为障碍以及日常生活活动能力的逐渐受损。目前的药物治疗仅限于对症干预,但不能预防进行性神经元变性。因此,需要新的治疗策略来干预这些进行性的病理过程。在过去的几年中,腺苷作为一种广泛释放的嘌呤核糖核苷,因其具有神经调节能力及其在神经退行性疾病中的积极实验效果而变得重要。最近的研究表明,腺苷受体在调节认知功能方面发挥着重要作用。本文试图综述不同研究的已发表报告和数据,以证明腺苷能功能与 AD 相关认知缺陷之间存在关系。流行病学研究发现,咖啡(一种非选择性腺苷受体拮抗剂)的摄入与 AD 患者和老年人认知功能的改善有关。在转基因动物模型中,长期给予咖啡因可减少大脑中的淀粉样蛋白负担,提高认知能力。腺苷 A2A 受体拮抗剂模拟了咖啡因对认知功能的这些有益影响。在存在 A2A 受体拮抗剂的情况下,含有淀粉样β的神经元细胞培养物完全阻止了淀粉样β诱导的神经毒性。这些发现表明,腺苷能系统构成了 AD 的一个新的治疗靶点,咖啡因和 A2A 受体拮抗剂可能有希望用于治疗 AD 的认知功能障碍。