Reneerkens Olga A H, Rutten Kris, Steinbusch Harry W M, Blokland Arjan, Prickaerts Jos
Department of Neuroscience, Faculty of Health, Medicine and Life Sciences, School for Mental Health and Neuroscience, Maastricht University, P.O. Box 616, 6200 MD Maastricht, The Netherlands.
Psychopharmacology (Berl). 2009 Jan;202(1-3):419-43. doi: 10.1007/s00213-008-1273-x. Epub 2008 Aug 16.
One of the major complaints most people face during aging is an impairment in cognitive functioning. This has a negative impact on the quality of daily life and is even more prominent in patients suffering from neurodegenerative and psychiatric disorders including Alzheimer's disease, schizophrenia, and depression. So far, the majority of cognition enhancers are generally targeting one particular neurotransmitter system. However, recently phosphodiesterases (PDEs) have gained increased attention as a potential new target for cognition enhancement. Inhibition of PDEs increases the intracellular availability of the second messengers cGMP and/or cAMP.
The aim of this review was to provide an overview of the effects of phosphodiesterase inhibitors (PDE-Is) on cognition, the possible underlying mechanisms, and the relationship to current theories about memory formation.
Studies of the effects of inhibitors of different PDE families (2, 4, 5, 9, and 10) on cognition were reviewed. In addition, studies related to PDE-Is and blood flow, emotional arousal, and long-term potentiation (LTP) were described.
PDE-Is have a positive effect on several aspects of cognition, including information processing, attention, memory, and executive functioning. At present, these data are likely to be explained in terms of an LTP-related mechanism of action.
PDE-Is are a promising target for cognition enhancement; the most suitable candidates appear to be PDE2-Is or PDE9-Is. The future for PDE-Is as cognition enhancers lies in the development of isoform-specific PDE-Is that have limited aversive side effects.
大多数人在衰老过程中面临的主要问题之一是认知功能受损。这对日常生活质量有负面影响,在患有神经退行性疾病和精神疾病(包括阿尔茨海默病、精神分裂症和抑郁症)的患者中更为突出。到目前为止,大多数认知增强剂通常针对一种特定的神经递质系统。然而,最近磷酸二酯酶(PDEs)作为一种潜在的认知增强新靶点受到了越来越多的关注。抑制磷酸二酯酶可增加第二信使环鸟苷酸(cGMP)和/或环磷酸腺苷(cAMP)的细胞内可用性。
本综述的目的是概述磷酸二酯酶抑制剂(PDE-Is)对认知的影响、可能的潜在机制以及与当前记忆形成理论的关系。
综述了不同磷酸二酯酶家族(2、4、5、9和10)抑制剂对认知影响的研究。此外,还描述了与磷酸二酯酶抑制剂和血流、情绪唤醒及长时程增强(LTP)相关的研究。
磷酸二酯酶抑制剂对认知的多个方面有积极影响,包括信息处理、注意力、记忆和执行功能。目前,这些数据可能用与长时程增强相关的作用机制来解释。
磷酸二酯酶抑制剂是一种有前景的认知增强靶点;最合适的候选药物似乎是磷酸二酯酶2抑制剂(PDE2-Is)或磷酸二酯酶9抑制剂(PDE9-Is)。磷酸二酯酶抑制剂作为认知增强剂的未来在于开发具有有限厌恶副作用的亚型特异性磷酸二酯酶抑制剂。