Investigational phosphodiesterase inhibitors in phase I and phase II clinical trials for Alzheimer's disease

被引:145
作者
Prickaerts, Jos [1 ]
Heckman, Pim R. A. [1 ,2 ]
Blokland, Arjan [2 ]
机构
[1] Maastricht Univ, Sch Mental Hlth & Neurosci, Dept Psychiat & Neuropsychol, POB 616, NL-6200 MD Maastricht, Netherlands
[2] Maastricht Univ, Dept Neuropsychol & Psychopharmacol, Maastricht, Netherlands
关键词
Alzheimer's disease; cAMP; cGMP; cognition; mild cognitive impairment; neuroprotection; phosphodiesterase; CEREBRAL-BLOOD-FLOW; LONG-TERM-MEMORY; MOUSE MODEL; DOUBLE-BLIND; IMPROVES MEMORY; COGNITIVE PERFORMANCE; SYNAPTIC PLASTICITY; PDE4D INHIBITORS; ENHANCES MEMORY; 10A INHIBITORS;
D O I
10.1080/13543784.2017.1364360
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Phosphodiesterase (PDE) inhibitors improve signaling pathways in brain circuits by increasing intracellular cyclic adenosine monophosphate (cAMP) and/or cyclic guanosine monophosphate (cGMP). In the last decade, the first clinical studies investigating selective PDE inhibitors in Alzheimer's disease (AD) have been initiated, based on their positive effects on cognitive processes and neuroprotection in numerous animal studies.Areas covered: This article reviews the clinical studies investigating the pro-cognitive/neuroprotective effects of PDE inhibitors in patients with AD, as well as in age-associated memory impaired elderly and patients with mild cognitive impairment (MCI), the prodromal stage of AD. PDE inhibitors will also be discussed with respect to adverse effects including safety and tolerability.Expert opinion: The limited available data of clinical studies with PDE inhibitors tested in different populations of AD patients do not allow the drawing of any concrete conclusion yet. Currently, studies with a PDE3 (cilostazol) or PDE9 inhibitor (BI 409,306) are still ongoing in patients with MCI or AD, respectively. Studies with PDE4 inhibitors (HT-0712, roflumilast and BPN14770) in healthy elderly and elderly with age-associated memory impairments indicate that the optimum dose and/or inhibiting the most relevant PDE isoform hold great promise when tested in the appropriate population of patients with MCI or AD eventually.
引用
收藏
页码:1033 / 1048
页数:16
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