Selective phosphodiesterase inhibitors: a promising target for cognition enhancement

被引:223
作者
Reneerkens, Olga A. H. [1 ,3 ]
Rutten, Kris [1 ,3 ]
Steinbusch, Harry W. M. [1 ,3 ]
Blokland, Arjan [2 ]
Prickaerts, Jos [1 ,3 ]
机构
[1] Maastricht Univ, Dept Neurosci, Fac Hlth Med & Life Sci, Sch Mental Hlth & Neurosci, NL-6200 MD Maastricht, Netherlands
[2] Maastricht Univ, Dept Neuropsychol & Psychopharmacol, Fac Psychol & Neurosci, Sch Mental Hlth & Neurosci, NL-6200 MD Maastricht, Netherlands
[3] European Grad Sch Neurosci EURON, Maastricht, Netherlands
关键词
PDE inhibitors; Cognition; cAMP; cGMP; Memory; LTP; CYCLIC-NUCLEOTIDE PHOSPHODIESTERASE; LONG-TERM POTENTIATION; OBJECT RECOGNITION MEMORY; SIGNAL-TRANSDUCTION SYSTEM; MESSENGER-RNA EXPRESSION; CEREBRAL-BLOOD-FLOW; RADIAL-ARM MAZE; SPLICE VARIANTS; NITRIC-OXIDE; RAT-BRAIN;
D O I
10.1007/s00213-008-1273-x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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.
引用
收藏
页码:419 / 443
页数:25
相关论文
共 174 条
[71]   Molecular pharmacological dissection of short- and long-term memory [J].
Izquierdo, LA ;
Barros, DM ;
Vianna, MRM ;
Coitinho, A ;
Silva, TDE ;
Choi, H ;
Moletta, B ;
Medina, JH ;
Izquierdo, I .
CELLULAR AND MOLECULAR NEUROBIOLOGY, 2002, 22 (03) :269-287
[72]   Rolipram: A specific phosphodiesterase 4 inhibitor with potential antipsychotic activity [J].
Kanes, S. J. ;
Tokarczyk, J. ;
Siegel, S. J. ;
Bilker, W. ;
Abel, T. ;
Kelly, M. P. .
NEUROSCIENCE, 2007, 144 (01) :239-246
[73]   Mnemonic functions of the hippocampus: A comparison between animals and humans [J].
Kesner, Raymond P. ;
Hopkins, Ramona O. .
BIOLOGICAL PSYCHOLOGY, 2006, 73 (01) :3-18
[74]   Molecular comparison of rat cyclic nucleotide phosphodiesterase 8 family: unique expression of PDE8B in rat brain [J].
Kobayashi, T ;
Gamanuma, M ;
Sasaki, T ;
Yamashita, Y ;
Yuasa, K ;
Kotera, J ;
Omori, K .
GENE, 2003, 319 :21-31
[75]   Immunohistochemical localization of cGMP-binding cGMP-specific phosphodiesterase (PDE5) in rat tissues [J].
Kotera, J ;
Fujishige, K ;
Omori, K .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 2000, 48 (05) :685-693
[76]   Central regulation of autonomic function: No brakes? [J].
Krukoff, TL .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 1998, 25 (06) :474-478
[77]   The phosphodiesterase 5 inhibitor sildenafil has no effect on cerebral blood flow or blood velocity, but nevertheless induces headache in healthy subjects [J].
Kruuse, C ;
Thomsen, LL ;
Jacobsen, TB ;
Olesen, J .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2002, 22 (09) :1124-1131
[78]  
Kurt M, 2004, POL J PHARMACOL, V56, P353
[79]   Immunohistochemical localization of calmodulin-dependent cyclic phosphodiesterase in the human brain [J].
Lal, S ;
Sharma, RK ;
McGregor, C ;
Macaulay, RJB .
NEUROCHEMICAL RESEARCH, 1999, 24 (01) :43-49
[80]   Isolation and characterization of PDE10A, a novel human 3′, 5′-cyclic nucleotide phosphodiesterase [J].
Loughney, K ;
Snyder, PB ;
Uher, L ;
Rosman, GJ ;
Ferguson, K ;
Florio, VA .
GENE, 1999, 234 (01) :109-117