Brucine N-Oxide Reduces Ethanol Intake and Preference in Alcohol-Preferring Male Fawn-Hooded Rats. 2020

Shoupeng Wei, and Yu-Ling Li, and Qi Gong, and Hui Liang, and Qing Liu, and Rick E Bernardi, and Han-Ting Zhang, and Feng Chen, and Andrew J Lawrence, and Jian-Hui Liang
From the, Department of Pharmacology, (SW, QG, HL, QL), School of Basic Medicine Sciences, Peking University, Beijing, China.

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. 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). 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. BNO may help to control excessive alcohol use and should be considered a treatment strategy for future study and development.

UI MeSH Term Description Entries
D008124 Locomotion Movement or the ability to move from one place or another. It can refer to humans, vertebrate or invertebrate animals, and microorganisms. Locomotor Activity,Activities, Locomotor,Activity, Locomotor,Locomotor Activities
D008297 Male Males
D002492 Central Nervous System Depressants A very loosely defined group of drugs that tend to reduce the activity of the central nervous system. The major groups included here are ethyl alcohol, anesthetics, hypnotics and sedatives, narcotics, and tranquilizing agents (antipsychotics and antianxiety agents). CNS Depressants,Depressants, CNS
D003497 Cyclic N-Oxides Heterocyclic compounds in which an oxygen is attached to a cyclic nitrogen. Heterocyclic N-Oxides,Cyclic N Oxides,Heterocyclic N Oxides,N Oxides, Cyclic,N-Oxides, Cyclic,N-Oxides, Heterocyclic,Oxides, Cyclic N
D000082563 Open Field Test A maze test in which an animal is placed in an open chamber designed to assess anxiety and exploratory behavior by movement patterns. In novel object recognition test various objects are added to open field to assess exploration and memory. Novel Object Recognition Test,Open Field Maze Test,Open Field Tests,Test, Open Field
D000428 Alcohol Drinking Behaviors associated with the ingesting of ALCOHOLIC BEVERAGES, including social drinking. Alcohol Consumption,Alcohol Intake,Drinking, Alcohol,Alcohol Drinking Habits,Alcohol Drinking Habit,Alcohol Intakes,Consumption, Alcohol,Drinking Habit, Alcohol,Habit, Alcohol Drinking,Habits, Alcohol Drinking,Intake, Alcohol
D000431 Ethanol A clear, colorless liquid rapidly absorbed from the gastrointestinal tract and distributed throughout the body. It has bactericidal activity and is used often as a topical disinfectant. It is widely used as a solvent and preservative in pharmaceutical preparations as well as serving as the primary ingredient in ALCOHOLIC BEVERAGES. Alcohol, Ethyl,Absolute Alcohol,Grain Alcohol,Alcohol, Absolute,Alcohol, Grain,Ethyl Alcohol
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D001522 Behavior, Animal The observable response an animal makes to any situation. Autotomy Animal,Animal Behavior,Animal Behaviors
D012646 Self Administration Administration of a drug or chemical by the individual under the direction of a physician. It includes administration clinically or experimentally, by human or animal. Administration, Self,Administrations, Self,Self Administrations

Related Publications

Shoupeng Wei, and Yu-Ling Li, and Qi Gong, and Hui Liang, and Qing Liu, and Rick E Bernardi, and Han-Ting Zhang, and Feng Chen, and Andrew J Lawrence, and Jian-Hui Liang
January 1991, Alcohol and alcoholism (Oxford, Oxfordshire). Supplement,
Shoupeng Wei, and Yu-Ling Li, and Qi Gong, and Hui Liang, and Qing Liu, and Rick E Bernardi, and Han-Ting Zhang, and Feng Chen, and Andrew J Lawrence, and Jian-Hui Liang
September 1997, Pharmacology, biochemistry, and behavior,
Shoupeng Wei, and Yu-Ling Li, and Qi Gong, and Hui Liang, and Qing Liu, and Rick E Bernardi, and Han-Ting Zhang, and Feng Chen, and Andrew J Lawrence, and Jian-Hui Liang
December 2012, Alcoholism, clinical and experimental research,
Shoupeng Wei, and Yu-Ling Li, and Qi Gong, and Hui Liang, and Qing Liu, and Rick E Bernardi, and Han-Ting Zhang, and Feng Chen, and Andrew J Lawrence, and Jian-Hui Liang
January 1990, Alcohol and alcoholism (Oxford, Oxfordshire),
Shoupeng Wei, and Yu-Ling Li, and Qi Gong, and Hui Liang, and Qing Liu, and Rick E Bernardi, and Han-Ting Zhang, and Feng Chen, and Andrew J Lawrence, and Jian-Hui Liang
October 1996, Psychopharmacology,
Shoupeng Wei, and Yu-Ling Li, and Qi Gong, and Hui Liang, and Qing Liu, and Rick E Bernardi, and Han-Ting Zhang, and Feng Chen, and Andrew J Lawrence, and Jian-Hui Liang
January 1991, Life sciences,
Shoupeng Wei, and Yu-Ling Li, and Qi Gong, and Hui Liang, and Qing Liu, and Rick E Bernardi, and Han-Ting Zhang, and Feng Chen, and Andrew J Lawrence, and Jian-Hui Liang
October 2014, European journal of pharmacology,
Shoupeng Wei, and Yu-Ling Li, and Qi Gong, and Hui Liang, and Qing Liu, and Rick E Bernardi, and Han-Ting Zhang, and Feng Chen, and Andrew J Lawrence, and Jian-Hui Liang
July 2020, The American journal of drug and alcohol abuse,
Shoupeng Wei, and Yu-Ling Li, and Qi Gong, and Hui Liang, and Qing Liu, and Rick E Bernardi, and Han-Ting Zhang, and Feng Chen, and Andrew J Lawrence, and Jian-Hui Liang
January 1998, Pharmacology, biochemistry, and behavior,
Shoupeng Wei, and Yu-Ling Li, and Qi Gong, and Hui Liang, and Qing Liu, and Rick E Bernardi, and Han-Ting Zhang, and Feng Chen, and Andrew J Lawrence, and Jian-Hui Liang
October 2005, Brain research,
Copied contents to your clipboard!