[1] Conti M, Richter W, Mehats C, et al. Cyclic AMP-specific PDE4 phosphodiesterases as critical components of cyclic AMP signaling[J]. J Biol Chem, 2003,278 (8): 5493-5496. [2] Greengard P. The neurobiology of slow synaptic transmission[J]. Science, 2001,294 (5544): 1024-1030. [3] Lesch KP, Lerer B. The 5-HT receptor-G-protein-effectorsystem complex in depression. Effect of glucocorticoids[J]. J Neural Transm Gen Sect, 1991,84 (1/2): 3-18. [4] Majewski HK, Musgrave IF. Second messenger pathways in themodulation of neurotransmitter release[J]. AustN Z J Med, 1995,25(6): 817-821. [5] Neve KA, Seamans JK, Trantham-Davidson H. Dopamine receptor signaling[J]. J Recept Signal Transduct Res, 2004,24(3): 165-205. [6] Teng FY, Tang BL. Axonal regeneration in adult CNS neurons-signaling molecules and pathways[J]. J Neurochem,2006, 96(6):1501-1508. [7] Houslay MD, Schafer P, Zhang KY. Keynote review: phosphodiesterase-4 as a therapeutic target[J]. Drug Discov Today,2005, 10(22): 1503-1519. [8] Conti M, Beavo J. Biochemistry and physiology of cyclic nucleotide phosphodiesterases: essential components in cyclic nucleotide signaling[J]. Annu Rev Biochem,2007,76(3): 481-511. [9] Bender AT, Beavo JA. Cyclic nucleotide phosphodiesterases: molecular regulation to clinical use[J]. Pharmacol Rev, 2006, 58(3): 488-520. [10] Esposito K, Reierson GW, Luo HR, et al. Phosphodiesterase genes and antidepressant treatment response: a review[J]. Ann Med, 2009, 41(11): 177-185. [11] Jager R, Schwede F, Genieser HG, et al. Activation of PDE2 and PDE5 by specific GAF ligands: delayed activation of PDE5[J]. Br J Pharmacol,2010,12(13): 123-132. [12] Pandit J, Forman MD, Fennell KF, et al. Mechanism for the allosteric regulation of phosphodiesterase 2A deduced from the X-ray structure of a near full-length construct[J]. PNAS,2009, 106(43): 18225-18230. [13] Aravind L, Ponting CP. The GAF domain: an evolutionary link between diverse phototransducing proteins[J]. Trends Biochem Sci ,1997,22: 458-459. [14] Kleppisch T. Phosphodiesterases in the central nervous system[J]. Handb Exp Pharmacol, 2009,12(191): 71-92. [15] Bender AT, Beavo JA. Cyclic nucleotide phosphodiesterases: molecular regulation to clinical use[J]. Pharmacol Rev,2006, 58(3): 488-520. [16] Boess FG, Hendrix M, van der Staay FJ, et al. Inhibition of phosphodiesterase 2 increases neuronal cGMP, synaptic plasticity and memory performance[J]. Neuropharmacology, 2004, 47(7): 1081-1092. [17] Blokland R, Schreiber R, Prickaerts J. Improving memory: a role for phosphodiesterases[J]. Curr Pharm Des,2006, 12(2): 2511-2523. [18] Tsai LC, Beavo JA. The roles of cyclic nucleotide phosphodiesterases (PDEs) in steroidogenesis[J].Curr Opin Pharmacol, 2011,11(6):670-675. [19] Pollatos O, Kopietz R, Linn J, et al. Emotional stimulation alters olfactory sensitivity and odor judgment[J]. Chem Senses, 2007, 32(6): 583-589. [20] Drobna E, Gazdag Z, Culakova H, et al. Overexpression of the YAP1, PDE2, and STB3 genes enhances the tolerance of yeast to oxidative stress induced by 7-chlorotetrazolo[5,1-c] benzo[1,2,4] triazine[J].FEMS Yeast Res, 2012, 12(8):958-968. [21] Suvarna NU, O'Donnell JM. Hydrolysis of N-Methyl-D-aspartate receptor-stimulated cAMP and cGMP by PDE4 and PDE2 phosphodiesterases in primary neuronal cultures of rat cerebral cortex and hippocampus[J]. J Pharmacol Exp Ther, 2002, 302(4): 249-256. [22] Masood A, Huang Y, Hajjhussein H, et al. Anxiolytic effects of phosphodiesterase-2 inhibitors associated with increased cGMP signaling[J]. J Pharmacol Exp Ther, 2009, 331(2): 690-699. [23] Pelligrino DA, Wang Q. Cyclic nucleotide crosstalk and the regulation of cerebral vasodilation[J]. Prog Neurobiol,1998, 56(7): 1-18. [24] Heine C, Sygnecka K, Scherf N, et al. Phosphodiesterase 2 inhibitors promote axonal outgrowth in organotypic slice co-cultures[J]. Neurosignals, 2013,21(3/4):197-212. [25] Deng C, Wang D, Bugaj-Gaweda B, et al. Assays for cyclic nucleotide-specific phosphodiesterases (PDEs) in the central nervous system (PDE1, PDE2, PDE4, and PDE10)[J]. Curr Protoc Neurosci, 2007, 7(2): 7-21. [26] Boess FG, Hendrix M, van der Staay FJ, et al. Inhibition of phosphodiesterase 2 increases neuronal cGMP, synaptic plasticity and memory performance[J]. Neuropharmacology, 2004,47(7):1081-1092. [27] Sierksma AS, Rutten K, Sydlik S, et al. Chronic phosphodiesterase type 2 inhibition improves memory in the APPswe/PS1dE9 mouse model of Alzheimer's disease[J]. Neuropharmacology,2013, 64:124-136. [28] O'Donnell JM, Zhang HT. Antidepressant effects of inhibitors of cAMP phosphodiesterase (PDE4)[J]. Trends Pharmacol Sci, 2004, 25(3): 158-163. [29] Pérez-Torres S, Miró X, Palacios JM, et al. Phosphodiesterase type 4 isozymes expression in human brain examined by in situ hybridization histochemistry and[3H] rolipram binding autoradiography. Comparison with monkey and rat brain[J]. J Chem Neuroanat, 2000, 20(3/4): 349-374. [30] Reneerkens OA, Rutten K, Bollen E, et al. Inhibition of phoshodiesterase type 2 or type 10 reverses object memory deficits induced by scopolamine or MK-801[J]. Behav Brain Res, 2013, 236(1):16-22. [31] Masood A, Nadeem A, Mustafa SJ, et al. Reversal of oxidative stress-induced anxiety by inhibition of phosphodiesterase-2 in mice[J]. J Pharmacol Exp Ther, 2008, 326(2): 369-379. [32] Mattson MP, Maudsley S, Martin B. BDNF and 5-HT: adynamic duo in age-related neuronal plasticity andneurodegenerative disorders[J]. Trends Neurosci, 2004,27(3), 589-594. [33] Banasr M, Hery M, Printemps R, et al. Serotonin-induced increases in adult cell proliferation andneurogenesis are mediated through different and common5-HT receptor subtypes in the dentate gryus and thesubventricular zone[J].Neuropsychopharmacology, 2004, 29(3):450-460. [34] Yuasa K, Kanoh Y, Okumura K, et al. Genomic organization of the human phosphodiesterase PDE11A gene, Evolutionary relatedness with other PDEs containing GAF domains[J]. Eur J Biochem, 2001, 268(1): 168-178. [35] Bon CL, Garthwaite J. On the role of nitric oxide in hippocampal long-term potentiation[J]. J Neurosci, 2003,23(1): 1941-1948. [36] Zhang HT, Huang Y, Jin SL, et al. Antidepressant-like profile and reduced sensitivity to rolipram in mice deficient in the PDE4D phosphodiesterase enzyme[J]. Neuropsychopharmacology, 2002, 27(4): 587-595. [37] Zhang HT, Zhao Y, Huang Y, et al. Inhibition of the phosphodiesterase 4 (PDE4) enzyme reverses memory deficits produced by infusion of the MEK inhibitor U0126 into the CA1 subregion of the rat hippocampus[J]. Neuropsychopharmacology, 2004, 29(8):1432-1439. [38] Zhang HT, Huang Y, Suvarna NU, et al. Effects of the novel PDE4 inhibitors MEM1018 and MEM1091 on memory in the radial-arm maze and inhibitory avoidance tests in rats[J]. Psychopharmacology, 2005, 179(3): 613-619. [39] Pickard BS, Thomson PA, Christoforou A, et al. The PDE4B gene confers sex-specific protection against schizophrenia[J]. Psychiatr Genet, 2007, 17(3):129-133. [40] Pilz RB, Broderick KE. Role of cyclic GMP in gene regulation[J]. Front Biosci, 2005, 10: 1239-1268. |