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磷酸二酯酶与认知加工:超越记忆领域

PDE and cognitive processing: beyond the memory domain.

作者信息

Heckman P R A, Blokland A, Ramaekers J, Prickaerts J

机构信息

Department of Psychiatry and Neuropsychology, School for Mental Health and Neuroscience, Maastricht University, 6200 MD Maastricht, The Netherlands; Department of Neuropsychology and Psychopharmacology, Maastricht University, 6200 MD Maastricht, The Netherlands.

Department of Neuropsychology and Psychopharmacology, Maastricht University, 6200 MD Maastricht, The Netherlands.

出版信息

Neurobiol Learn Mem. 2015 Mar;119:108-22. doi: 10.1016/j.nlm.2014.10.011. Epub 2014 Nov 13.

Abstract

Phosphodiesterase inhibitors (PDE-Is) enhance cAMP and/or cGMP signaling via reducing the degradation of these cyclic nucleotides. Both cAMP and cGMP signaling are essential for a variety of cellular functions and exert their effects both pre- and post-synaptically. Either of these second messengers relays and amplifies incoming signals at receptors on the cell surface making them important elements in signal transduction cascades and essential in cellular signaling in a variety of cell functions including neurotransmitter release and neuroprotection. Consequently, these processes can be influenced by PDE-Is as they increase cAMP and/or cGMP concentrations. PDE-Is have been considered as possible therapeutic agents to treat impaired memory function linked to several brain disorders, including depression, schizophrenia and Alzheimer's disease (AD). This review will, however, focus on the possible role of phosphodiesterases (PDEs) in cognitive decline beyond the memory domain. Here we will discuss the involvement of PDEs on three related domains: attention, information filtering (sensory- and sensorimotor gating) and response inhibition (drug-induced hyperlocomotion). Currently, these are emerging cognitive domains in the field of PDE research. Here we discuss experimental studies and the potential beneficial effects of PDE-I drugs on these cognitive domains, as effects of PDE-Is on these domains could potentially influence effects on memory performance. Overall, PDE4 seems to be the most promising target for all domains discussed in this review.

摘要

磷酸二酯酶抑制剂(PDE-Is)通过减少这些环核苷酸的降解来增强环磷酸腺苷(cAMP)和/或环磷酸鸟苷(cGMP)信号传导。cAMP和cGMP信号传导对于多种细胞功能都至关重要,并且在突触前和突触后都发挥作用。这两种第二信使中的任何一种都能在细胞表面的受体处中继和放大传入信号,使其成为信号转导级联反应中的重要元素,并且在包括神经递质释放和神经保护在内的多种细胞功能的细胞信号传导中必不可少。因此,这些过程会受到PDE-Is的影响,因为它们会增加cAMP和/或cGMP的浓度。PDE-Is被认为是治疗与多种脑部疾病相关的记忆功能受损的潜在治疗药物,这些疾病包括抑郁症、精神分裂症和阿尔茨海默病(AD)。然而,本综述将聚焦于磷酸二酯酶(PDEs)在超出记忆领域的认知衰退中的可能作用。在此,我们将讨论PDEs在三个相关领域的参与情况:注意力、信息过滤(感觉和感觉运动门控)以及反应抑制(药物诱导的活动亢进)。目前,这些是PDE研究领域中正在兴起的认知领域。我们在此讨论实验研究以及PDE-I药物对这些认知领域的潜在有益作用,因为PDE-Is对这些领域的作用可能会潜在地影响对记忆表现的作用。总体而言,PDE4似乎是本综述中所讨论的所有领域最有前景的靶点。

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