Ghavami Afshin, Hirst Warren D, Novak Thomas J
Neuroscience Discovery Research, Wyeth Research, Monmouth Junction, New Jersey 08852-2718, USA.
Drugs R D. 2006;7(2):63-71. doi: 10.2165/00126839-200607020-00001.
Phosphodiesterase-4 (PDE4) belongs to an important family of proteins that regulates the intracellular level of cyclic adenosine monophosphate (cAMP). Several lines of evidence indicate that targeting PDE4 with selective inhibitors may offer novel strategies in the treatment of age-related memory impairment and Alzheimer's disease. The rationale for such an approach stems from preclinical studies indicating that PDE4 inhibitors can counteract deficits in long-term memory caused by pharmacological agents, aging or overexpression of mutant forms of human amyloid precursor proteins. In addition to their pro-cognitive and pro-synaptic plasticity properties, PDE4 inhibitors are potent neuroprotective, neuroregenerative and anti-inflammatory agents. Based on the fact that Alzheimer's disease is a progressive neurodegenerative disorder that is characterised by cognitive impairment, and that neuroinflammation is now recognised as a prominent feature in Alzheimer's pathology, we have concluded that targeting PDE4 with selective inhibitors may offer a novel therapy aimed at slowing progression, prevention and, eventually, therapy of Alzheimer's disease.
磷酸二酯酶-4(PDE4)属于一类重要的蛋白质家族,可调节细胞内环磷酸腺苷(cAMP)的水平。多项证据表明,用选择性抑制剂靶向PDE4可能为治疗与年龄相关的记忆障碍和阿尔茨海默病提供新策略。这种方法的理论依据来自临床前研究,表明PDE4抑制剂可以抵消由药物、衰老或人类淀粉样前体蛋白突变形式的过表达引起的长期记忆缺陷。除了具有促认知和促突触可塑性特性外,PDE4抑制剂还是有效的神经保护、神经再生和抗炎剂。鉴于阿尔茨海默病是一种以认知障碍为特征的进行性神经退行性疾病,且神经炎症现已被认为是阿尔茨海默病病理学的一个突出特征,我们得出结论,用选择性抑制剂靶向PDE4可能提供一种旨在减缓疾病进展、预防并最终治疗阿尔茨海默病的新疗法。