Institute of Pharmacology and Neurosciences, Faculty of Medicine and Unit of Neurosciences, Institute of Molecular Medicine, University of Lisbon, Lisbon, Portugal.
J Alzheimers Dis. 2010;20 Suppl 1:S3-15. doi: 10.3233/JAD-2010-1379.
Caffeine causes most of its biological effects via antagonizing all types of adenosine receptors (ARs): A1, A2A, A3, and A2B and, as does adenosine, exerts effects on neurons and glial cells of all brain areas. In consequence, caffeine, when acting as an AR antagonist, is doing the opposite of activation of adenosine receptors due to removal of endogenous adenosinergic tonus. Besides AR antagonism, xanthines, including caffeine, have other biological actions: they inhibit phosphodiesterases (PDEs) (e.g., PDE1, PDE4, PDE5), promote calcium release from intracellular stores, and interfere with GABA-A receptors. Caffeine, through antagonism of ARs, affects brain functions such as sleep, cognition, learning, and memory, and modifies brain dysfunctions and diseases: Alzheimer's disease, Parkinson's disease, Huntington's disease, Epilepsy, Pain/Migraine, Depression, Schizophrenia. In conclusion, targeting approaches that involve ARs will enhance the possibilities to correct brain dysfunctions, via the universally consumed substance that is caffeine.
咖啡因通过拮抗所有类型的腺苷受体(AR)发挥其大部分生物学作用:A1、A2A、A3 和 A2B,并且像腺苷一样,对所有脑区的神经元和神经胶质细胞发挥作用。因此,咖啡因作为 AR 拮抗剂,通过去除内源性腺苷能紧张来拮抗腺苷受体的激活,从而产生相反的作用。除了 AR 拮抗作用外,黄嘌呤类物质(包括咖啡因)还具有其他生物学作用:它们抑制磷酸二酯酶(PDEs)(如 PDE1、PDE4、PDE5),促进细胞内储存的钙释放,并干扰 GABA-A 受体。咖啡因通过拮抗 AR 影响睡眠、认知、学习和记忆等大脑功能,并调节大脑功能障碍和疾病:阿尔茨海默病、帕金森病、亨廷顿病、癫痫、疼痛/偏头痛、抑郁、精神分裂症。总之,通过靶向涉及 AR 的方法,通过普遍摄入的物质咖啡因,有可能纠正大脑功能障碍。