The phosphodiesterase-4 inhibitor roflumilast decreases ethanol consumption in C57BL/6J mice

被引:28
|
作者
Liu, Xin [1 ,2 ,3 ]
Hao, Pi-Da [1 ]
Yang, Ming-Feng [1 ]
Sun, Jing-Yi [1 ]
Mao, Lei-Lei [1 ]
Fan, Cun-Dong [1 ]
Zhang, Zong-Yong [1 ]
Li, Da-Wei
Yang, Xiao-Yi [1 ]
Sun, Bao-Liang [1 ,4 ]
Zhang, Han-Ting [2 ,5 ,6 ]
机构
[1] Taishan Med Univ, Univ Shandong, Inst Neurol Disorders, Key Lab Cerebral Microcirculat, Tai An 271000, Shandong, Peoples R China
[2] Taishan Med Univ, Inst Pharmacol, Tai An 271016, Shandong, Peoples R China
[3] Taishan Med Univ, Sch Basic Med Sci, Dept Med Psychol, Tai An 271000, Shandong, Peoples R China
[4] Taishan Med Univ, Affiliated Hosp, Dept Neurol, Tai An 271000, Shandong, Peoples R China
[5] West Virginia Univ, Hlth Sci Ctr, Blanchette Rockefeller Neurosci Inst, Dept Behav Med & Psychiat, Morgantown, WV 26506 USA
[6] West Virginia Univ, Hlth Sci Ctr, Blanchette Rockefeller Neurosci Inst, Dept Physiol & Pharmacol, Morgantown, WV 26506 USA
基金
中国国家自然科学基金;
关键词
cAMP signaling; Phosphodiesterase-4 (PDE4); Roflumilast; C57BL/6J mice; Ethanol consumption; ELEMENT-BINDING PROTEIN; ALCOHOL-DRINKING; MEMORY FUNCTION; CAMP RESPONSE; ROLIPRAM; PDE4; ANXIETY; ANTIDEPRESSANT; DEFICITS; RATS;
D O I
10.1007/s00213-017-4631-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Rationale Alcohol use disorders have become one of the most damaging psychiatric disorders in the world; however, there are no ideal treatments in clinic. Phosphodiesterase-4 (PDE4), an enzyme that specifically hydrolyzes intracellular cyclic AMP (cAMP), has been involved in alcohol use disorders. Roflumilast is the first PDE4 inhibitor approved for treatment of chronic obstructive pulmonary diseases in clinic. It was of particular interest to researchers to determine whether roflumilast altered ethanol consumption. Objectives The present study tried to determine the effects of roflumilast on ethanol intake and preference. Methods We used the two-bottle choice paradigm to assess ethanol intake and preference in C57BL/6J mice treated with roflumilast (1, 3, or 10 mg/kg) or rolipram (0.5 mg/kg; positive control). The effect of roflumilast was verified using the ethanol drinking-in-dark (DID) test. Locomotor activity was examined using the open-field test. Intake of sucrose or quinine was also tested to determine whether natural reward preference and aversive stimuli were involved in the effect of PDE4 inhibitors. Results Similar to rolipram, roflumilast decreased ethanol intake and preference in two-bottle choice and DID tests in a dose-dependent manner, with significant changes at the dose of 10 mg/kg; in contrast, roflumilast did not affect sucrose or quinine drinking, although it decreased locomotor activity at the high dose within 3 h of treatment. Conclusions These data provide novel demonstration for the effect of roflumilast on ethanol consumption and suggest that roflumilast may be beneficial for treatment of alcoholism.
引用
收藏
页码:2409 / 2419
页数:11
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