Legacy Research, R.S Dow Neurobiology Laboratories, 1225 NE 2nd Avenue, Portland OR 97232, USA.
Curr Neuropharmacol. 2009 Sep;7(3):207-16. doi: 10.2174/157015909789152119.
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.
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。