参考文献/References:
[1]黄浩.以磷酸二酯酶为主要靶点的阿魏酸抗阿尔兹海默病作用机制研究[D]. 北京:北京工业大学,2016.
[2]万素馨,方伟. 阿尔茨海默病的治疗药物作用机制研究进展[J]. 现代药物与临床,2018,33(12):3406-3410.
[3]ADLIMOGHADDAM A, NEUENDORF M,ROY B,et a1.A review of clinical treatment considerations of donepezil in severe Alzheimer’s disease[J].CNS Neurosci Ther, 2018,24(10):876-888.
[4]LOVESTONE S,BOADA M,DUBOIS B,et a1.A phase II trial of tideglusib in Alzheimer’s disease[J].Alzheimers Dis,2015,45(1):75-88.
[5]MATHURAM T L,REECE L M,CHERIAN K M.GSK-3inhibitors:a double edged sword-an updam on tideglusib[J].Drug Res(Stuttg),2018,68(8):436-443.
[6]张莉,杜冠华. 磷酸二酯7:一个新的抗炎免疫药物靶点研究进展[J]. 中国药理学通报,2009,25(1):1-4.
[7]XU Y, ZHANG H T,ODONNELL J M. Phosphodiesterases in the central nervous system:implications in mood and cognitive disorders[J]. Handb Exp Pharmacol,2011(204):447-485.
[8]HECKMAN P R,BLOKLAND A,RAMAEKERS J,et al. PDE and cognitive processing:beyond the memory domain[J]. Neurobiol Learn Mem,2015(119):108-122.
[9]BENDER A T, BEAVO J A. Cyclic nucleotide phosphodiesterases: molecular regulation to clinical use[J]. Pharmacol Rev,2006,58(3):488-520.
[10]JUNG W Y, KIM H, PARK H J,et al. The ethanolic extract of the Eclipat prostrata L. ameliorates the cognitive impairment in mice induced by scopolamine[J]. Journal of Ethnopharmacology, 2016,190:165-173.
[11]GINTER E,SIMKO V,WEINREBOVA D,et al. Novel potential for the management of Alzheimer disease[J]. Bratisl Lek Listy,2015,116(10):580-581.
[12]ROULEAU N,TUROTTE S,MONDOU M H,et al. Development of a versatile platform for nuclear receptor screening using AlphaScreen[J]. J Biomol Screen,2003,8:191-197.
[13]BERNABEU R,SCHMITZ P, FAILLACE M P,et al. Hippocampal cGMP and cAMP are differentially involved in memory processing of inhibitory avoidance learning[J]. Neuroreport,1996,7:585-588.
[14]MORITA H,MURATA T,SHIMIZU K,et al. Characterization of phosphodiesterase 2A in human malignant melanoma PMP cells[J]. Oncol REP,2013,29(4):1275-1284.
[15]RENEERKENS O A,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.
[16]LUGNIER C.Cyclic nucleotide phosphodiesterase(PDE)super family:a new target for the development of specific therapeuticgents[J].Pharmacol Ther,2006,109(3):366-398.
[17]GOMEZ L, MASSARI M E, VICKERS T, et al. Design and synthesis of novel and selective phosphodiesterase 2(PDE2a)inhibitors for the treatment of memory disorders[J]. J Med Chem,2017,60(5):2037-2051.
[18]MENNITI F S, FARACI W S, SCHMIDT C J. Phosphodiesterases in the CNS: targets for drug development[J]. Nat Rev Drug Discovery,2006,5(8):660-670.
[19]LUEPTOW L M, ZHAN C G, O’DONNELL J M. Cyclic GMP-mediated memory enhancement in the object recognition test by inhibitors of phosphodiesterase-2 in mice[J]. Psychopharmacology,2016,233(3):447-456.
[20]BOESS F G, HENDRIX M, VANDERSTAAY F J, et al. Inhibition of phosphodiesterase 2 increases neuronal cGMP, synaptic plasticity and memory performance[J]. Neuropharmacology,2004,47(7):1081-1092.