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Phosphodiesterase Type 4 Inhibition in CNS Diseases
被引:48
作者:
Blokland, Arjan
[1
]
Heckman, Pim
[2
]
Vanmierlo, Tim
[3
,4
]
Schreiber, Rudy
[1
]
Paes, Dean
[3
,4
]
Prickaerts, Jos
[4
]
机构:
[1] Maastricht Univ, Fac Psychol & Neurosci, EURON, Dept Neuropsychol & Psychopharmacol, Maastricht, Netherlands
[2] Univ Groningen, Neurobiol Expertise Grp, Groningen Inst Evolutionary Life Sci GELIFES, Fac Sci & Engn, Groningen, Netherlands
[3] Hasselt Univ, Biomed Res Inst, Dept Immunol & Biochem, Hasselt, Belgium
[4] Maastricht Univ, EURON, Sch Mental Hlth & Neurosci, Dept Psychiat & Neuropsychol, Maastricht, Netherlands
关键词:
SUBCELLULAR-LOCALIZATION;
THERAPEUTIC STRATEGY;
STRUCTURAL BASIS;
DOUBLE-BLIND;
CAMP;
BRAIN;
PDE4;
MEMORY;
BINDING;
HIPPOCAMPUS;
D O I:
10.1016/j.tips.2019.10.006
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Phosphodiesterases (PDEs) have been an interesting drug target for many diseases. Although a vast number of mainly preclinical studies demonstrates beneficial effects of PDE inhibitors for central nervous system (CNS) diseases, no drugs are currently available for CNS indications. In this review, we discuss the rationale of PDE4 inhibitors for different CNS diseases, including memory impairments, striatal disorders, multiple sclerosis (MS), and acquired brain injury (ABU). However, clinical development has been problematic due to mechanism-based adverse effects of these drugs in humans. Our increased understanding of factors influencing the conformational state of the PDE4 enzyme and of how to influence the binding affinity of PDE4 subtype inhibitors, holds promise for the successful development of novel selective PDE4 inhibitors with higher efficacy and fewer adverse effects.
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页码:971 / 985
页数:15
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