Antidepressant effects of inhibitors of cAMP phosphodiesterase (PDE4)

被引:243
作者
O'Donnell, JM [1 ]
Zhang, HT [1 ]
机构
[1] Univ Tennessee, Ctr Hlth Sci, Dept Pharmacol, Memphis, TN 38163 USA
关键词
D O I
10.1016/j.tips.2004.01.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Despite initial promise, the development of type 4 phosphodiesterase (PDE4) inhibitors as antidepressants has not advanced significantly. This is due to an incomplete understanding of the functional importance of PDE4 subtypes and high-affinity and low-affinity inhibitor-binding conformers. However, recent developments have rekindled interest in the therapeutic potential of PDE4 inhibitors. First, PDE4 has been shown to be involved in cAMP signaling pathways that are affected by antidepressants. Second, data obtained using mouse knockout lines indicate that PDE4D and PDE4B mediate antidepressant effects. Third, it appears that the interaction of inhibitors with the high-affinity binding conformer of PDE4 is particularly important for antidepressant efficacy. These developments highlight the difficulties of dissociating the actions of PDE4 inhibitors and provide a guide for future research.
引用
收藏
页码:158 / 163
页数:6
相关论文
共 59 条
[11]  
Francis SH, 2001, PROG NUCLEIC ACID RE, V65, P1
[12]  
FRAZER A, 1997, J CLIN PSYCHOPHAR S1, V17, P2
[13]   Phosphodiesterase 4 inhibitors and the treatment of asthma - Where are we now and where do we go from here? [J].
Giembycz, MA .
DRUGS, 2000, 59 (02) :193-212
[14]   The MAP kinase ERK2 inhibits the cyclic AMP-specific phosphodiesterase HSPDE4D3 by phosphorylating it at Ser579 [J].
Hoffmann, R ;
Baillie, GS ;
MacKenzie, SJ ;
Yarwood, SJ ;
Houslay, MD .
EMBO JOURNAL, 1999, 18 (04) :893-903
[15]   PDE4 cAMP-specific phosphodiesterases [J].
Houslay, MD .
PROGRESS IN NUCLEIC ACID RESEARCH AND MOLECULAR BIOLOGY, VOL 69, 2001, 69 :249-315
[16]  
Houslay MD, 2003, BIOCHEM J, V370, P1, DOI 10.1042/bj20021698
[17]   Characterization of the rolipram-sensitive, cyclic AMP-specific phosphodiesterases: Identification and differential expression of immunologically distinct forms in the rat brain [J].
Iona, S ;
Cuomo, M ;
Bushnik, T ;
Naro, F ;
Sette, C ;
Hess, M ;
Shelton, ER ;
Conti, M .
MOLECULAR PHARMACOLOGY, 1998, 53 (01) :23-32
[18]  
Jacobitz S, 1996, MOL PHARMACOL, V50, P891
[19]   Localization of phosphodiesterase-4 isoforms in the medulla and nodose ganglion of the squirrel monkey [J].
Lamontagne, S ;
Meadows, E ;
Luk, P ;
Normandin, D ;
Muise, E ;
Boulet, L ;
Pon, DJ ;
Robichaud, A ;
Robertson, GS ;
Metters, KM ;
Nantel, F .
BRAIN RESEARCH, 2001, 920 (1-2) :84-96
[20]   CLINICAL AND BIOCHEMICAL EFFECTS OF THE SELECTIVE PHOSPHODIESTERASE INHIBITOR ROLIPRAM IN DEPRESSED INPATIENTS CONTROLLED BY DETERMINATION OF PLASMA-LEVEL [J].
LAUX, G ;
BECKER, T ;
KUHNE, G ;
LESCH, KP ;
RIEDERER, P ;
BECKMANN, H .
PHARMACOPSYCHIATRY, 1988, 21 (06) :378-379