Medina Alexandre E
Department of Anatomy and Neurobiology, Virginia Commonwealth University Medical Center Richmond, VA, USA.
Front Neurosci. 2011 Feb 18;5:21. doi: 10.3389/fnins.2011.00021. eCollection 2011.
Neuronal plasticity is an essential property of the brain that is impaired in different neurological conditions. Phosphodiesterase type 1 (PDE1) inhibitors can enhance levels of the second messengers cAMP/cGMP leading to the expression of neuronal plasticity-related genes, neurotrophic factors, and neuroprotective molecules. These neuronal plasticity enhancement properties make PDE1 inhibitors good candidates as therapeutic agents in many neurological conditions. However, the lack of specificity of the drugs currently available poses a challenge to the systematic evaluation of the beneficial effect of these agents. The development of more specific drugs may pave the way for the use of PDE1 inhibitors as therapeutic agents in cases of neurodevelopmental conditions such as fetal alcohol spectrum disorders and in degenerative disorders such as Alzheimer's and Parkinson's.
神经元可塑性是大脑的一种基本特性,在不同的神经疾病中会受到损害。1型磷酸二酯酶(PDE1)抑制剂可提高第二信使cAMP/cGMP的水平,从而导致与神经元可塑性相关的基因、神经营养因子和神经保护分子的表达。这些增强神经元可塑性的特性使PDE1抑制剂成为许多神经疾病治疗药物的理想候选者。然而,目前可用药物缺乏特异性,这对系统评估这些药物的有益效果构成了挑战。开发更具特异性的药物可能为在诸如胎儿酒精谱系障碍等神经发育疾病以及诸如阿尔茨海默病和帕金森病等退行性疾病中使用PDE1抑制剂作为治疗药物铺平道路。