Brucine N-Oxide Reduces Ethanol Intake and Preference in Alcohol-Preferring Male Fawn-Hooded Rats

被引:6
|
作者
Wei, Shoupeng [1 ]
Li, Yu-ling [2 ]
Gong, Qi [1 ]
Liang, Hui [1 ]
Liu, Qing [1 ]
Bernardi, Rick E. [3 ]
Zhang, Han-Ting [4 ,5 ]
Chen, Feng [6 ]
Lawrence, Andrew J. [6 ]
Liang, Jian-hui [7 ]
机构
[1] Peking Univ, Sch Basic Med Sci, Dept Pharmacol, Beijing, Peoples R China
[2] Tongji Univ, Sch Med, East Hosp, Dept Pharm, Shanghai, Peoples R China
[3] Heidelberg Univ, Cent Inst Mental Hlth, Med Fac Mannheim, Mannheim, Germany
[4] West Virginia Univ, Hlth Sci Ctr, Dept Behav Med & Psychiat, Morgantown, WV 26506 USA
[5] West Virginia Univ, Hlth Sci Ctr, Dept Physiol & Pharmacol, Morgantown, WV 26506 USA
[6] Univ Melbourne, Florey Inst Neurosci & Mental Hlth, Parkville, Vic 3010, Australia
[7] Peking Univ, Sch Pharmaceut Sci, Dept Mol & Cellular Pharmacol, Beijing 100191, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
Brucine N-Oxide; Alcohol; Alcohol Use Disorder; Fawn-Hooded (FH; Wjd) rat; Glycine Receptor; NONENZYMATIC REDUCTION; GLYCINE; DRINKING; ACAMPROSATE; MECHANISMS; STRYCHNINE; CANCER; METAANALYSIS; ENHANCEMENT; DEPRIVATION;
D O I
10.1111/acer.14344
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
Background Alcohol use disorder places a heavy burden on global public health systems and thus is in urgent need of improved pharmacotherapies. Previously, our group has demonstrated that 30 mg/kg of the indole alkaloid brucine significantly attenuates alcohol-drinking behavior; however, the high toxicity, poor water solubility, short half-life, and limited therapeutic window of brucine restrain its clinical application as an antialcoholism medication. We subsequently hypothesized that the oxide of brucine (brucine N-oxide) would produce a similar behavioral effect without the risk profile associated with brucine. Methods Male Fawn-Hooded rats with high innate alcohol preference underwent 2-bottle choice procedures (Experiments 1 to 3). Experiment 1 examined the effects of 7 daily BNO injections of 0, 30, 50, or 70 mg/kg (s.c.) on voluntary alcohol consumption (n = 9/group). Experiment 2 evaluated the impact of a single dose of 0 or 70 mg/kg BNO on the increased alcohol intake induced by a 4-day alcohol deprivation (n = 8/group). Experiment 3 tested the effect of 7 daily BNO injections of 0 or 70 mg/kg (s.c.) on sucrose preference (n = 6/group). Experiment 4 measured the median lethal dose (LD50) values of BNO and brucine to compare their acute toxicity in rats. Experiment 5 tested whether BNO (0, 30, 50, and 70 mg/kg, s.c.) affected locomotor activity using an open-field paradigm (n = 8/group). Finally, Experiment 6 evaluated the possible conditioned rewarding effects of 0, 30, 50, and 70 mg/kg BNO using the conditioned place preference paradigm (n = 6/group). Results BNO administration dose-dependently attenuated alcohol consumption without affecting food intake, total fluid consumption, or the natural preference for a sucrose solution, with 70 mg/kg BNO reducing consumption by 22.8%. A single dose of 70 mg/kg BNO significantly inhibited the alcohol deprivation effect. The LD50 values of BNO and brucine in rats were determined to be 1,103.5 +/- 177.0 mg/kg and 264.6 +/- 17.7 mg/kg, respectively. Finally, BNO administration did not affect spontaneous locomotor activity or induce a place preference. Conclusions BNO may help to control excessive alcohol use and should be considered a treatment strategy for future study and development.
引用
收藏
页码:1321 / 1328
页数:8
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