Institute of Cardiovascular and Medical Science, College of Veterinary, Medical and Life Science, University of Glasgow, Glasgow, U.K.
Biochem Soc Trans. 2019 Oct 31;47(5):1557-1565. doi: 10.1042/BST20190763.
Phosphodiesterases (PDEs) have long been considered as targets for the treatment of Alzheimer's disease (AD) and a substantial body of evidence suggests that one sub-family from the super-family of PDEs, namely PDE4D, has particular significance in this context. This review discusses the role of PDE4 in the orchestration of cAMP response element binding signaling in AD and outlines the benefits of targeting PDE4D specifically. We examine the limited available literature that suggests PDE4 expression does not change in AD brains together with reports that show PDE4 inhibition as an effective treatment in this age-related neurodegenerative disease. Actually, aging induces changes in PDE4 expression/activity in an isoform and brain-region specific manner that proposes a similar complexity in AD brains. Therefore, a more detailed account of AD-related alterations in cellular/tissue location and the activation status of PDE4 is required before novel therapies can be developed to target cAMP signaling in this disease.
磷酸二酯酶(PDEs)长期以来一直被认为是治疗阿尔茨海默病(AD)的靶点,大量证据表明,该超家族中的一个亚家族,即 PDE4D,在这种情况下具有特殊意义。本文综述了 PDE4 在 AD 中 cAMP 反应元件结合信号转导中的作用,并概述了特异性靶向 PDE4D 的益处。我们研究了有限的可用文献,这些文献表明 AD 大脑中的 PDE4 表达没有改变,同时也有报道表明 PDE4 抑制是这种与年龄相关的神经退行性疾病的有效治疗方法。实际上,衰老以特定于亚型和脑区的方式诱导 PDE4 表达/活性的改变,这表明 AD 大脑中存在类似的复杂性。因此,在开发针对这种疾病中 cAMP 信号的新疗法之前,需要更详细地了解 AD 相关的 PDE4 在细胞/组织位置和激活状态方面的改变。