Cyclic nucleotide phosphodiesterases: potential therapeutic targets for alcohol use disorder

被引:24
作者
Wen, Rui-Ting [1 ]
Zhang, Fang-Fang [2 ]
Zhang, Han-Ting [2 ,3 ,4 ,5 ]
机构
[1] Peking Univ, Dept Pharm, Peoples Hosp, Beijing 100044, Peoples R China
[2] Qilu Med Univ, Inst Pharmacol, Tai An 271016, Shandong, Peoples R China
[3] West Virginia Univ, Rockefeller Neurosci Inst, Hlth Sci Ctr, Dept Behav Med, Morgantown, WV 26506 USA
[4] West Virginia Univ, Rockefeller Neurosci Inst, Hlth Sci Ctr, Dept Psychiat, Morgantown, WV 26506 USA
[5] West Virginia Univ, Rockefeller Neurosci Inst, Hlth Sci Ctr, Dept Physiol Pharmacol & Neurosci, Morgantown, WV 26506 USA
关键词
Alcohol use disorder (AUD); Central nervous system; Alcohol dependence; cAMP; cGMP; Phosphodiesterase (PDE); ELEMENT-BINDING PROTEIN; GENE-TRANSCRIPTION FACTOR; CONDITIONED PLACE PREFERENCE; INDUCED MOTOR INCOORDINATION; CEREBELLAR GRANULE CELLS; I ADENYLYL-CYCLASE; RAT-BRAIN; INHIBITOR ROLIPRAM; NUCLEUS-ACCUMBENS; MESSENGER-RNA;
D O I
10.1007/s00213-018-4895-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Alcohol use disorder (AUD), which combines the criteria of both alcohol abuse and dependence, contributes as an important causal factor to multiple health and social problems. Given the limitation of current treatments, novel medications for AUD are needed to better control alcohol consumption and maintain abstinence. It has been well established that the intracellular signal transduction mediated by the second messengers cyclic AMP (cAMP) and cyclic GMP (cGMP) crucially underlies the genetic predisposition, rewarding properties, relapsing features, and systemic toxicity of compulsive alcohol consumption. On this basis, the upstream modulators phosphodiesterases (PDEs), which critically control intracellular levels of cyclic nucleotides by catalyzing their degradation, are proposed to play a role in modulating alcohol abuse and dependent process. Here, we highlight existing evidence that correlates cAMP and cGMP signal cascades with the regulation of alcohol-drinking behavior and discuss the possibility that PDEs may become a novel class of therapeutic targets for AUD.
引用
收藏
页码:1793 / 1805
页数:13
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