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Oral Cannabidiol does not alter Alcohol Seeking and Self-Administration in Baboons
被引:4
|作者:
Moore, Catherine F.
[1
]
Zamarripa, C. Austin
[2
]
Weerts, Elise M.
[1
,2
,3
]
机构:
[1] Johns Hopkins Univ, Sch Med, Dept Psychiat & Behav Sci, Div Behav Biol, 5510 Nathan Shock Dr, Baltimore, MD 21224 USA
[2] Johns Hopkins Univ, Sch Med, Dept Psychiat & Behav Sci, Behav Pharmacol Res Unit, 5510 Nathan Shock Dr, Baltimore, MD 21224 USA
[3] Johns Hopkins Bayview Med Campus, Behav Biol Res Ctr, Dept Psychiat & Behav Sci, 5510 Nathan Shock Dr,Suite 3000, Baltimore, MD 21224 USA
基金:
美国国家卫生研究院;
关键词:
Alcohol;
Cannabidiol;
Reinforcement;
Self;
-administration;
Alcohol -related cues;
RECEPTOR ANTAGONIST;
ETHANOL INTAKE;
CONSUMPTION;
INHIBITION;
EXTINCTION;
NALTREXONE;
SR-141716;
SUCROSE;
D O I:
10.1016/j.drugalcdep.2023.109829
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: The cannabinoid cannabidiol (CBD) is currently under investigation as a pharmacotherapy for alcohol use disorder. The aim of the present study was to examine whether acute and chronic treatment with pure CBD would decrease alcohol seeking and consumption behaviors or alter drinking patterns in male baboons with extensive histories of daily alcohol intake (1 g/kg/day).Methods: Seven male baboons self-administered oral alcohol (4% w/v) in a validated chained schedule of rein-forcement (CSR) procedure that modeled periods of anticipation, seeking, and consumption. In Experiment 1, CBD (5-40 mg/kg) or vehicle (peanut oil, USP) was administered orally 15-or 90-minutes prior to the start of the session. In Experiment 2, oral doses of CBD (10-40 mg/kg) or vehicle were administered for 5 consecutive days during ongoing alcohol access under the CSR. In addition, behavioral observations were conducted to assess potential drug side effects (e.g., sedation, motor incoordination) following chronic CBD treatment immediately after the session and 24-hours after drug administration.Results: Across both experiments, baboons self-administered an average of 1 g/kg/day of alcohol under baseline conditions. Administration of acute or chronic CBD (150-1200 mg total CBD dose/day) that encompassed the purported therapeutic dose range did not significantly reduce alcohol seeking, self-administration or intake (g/ kg). Drinking patterns (i.e., number of drinks/bouts, bout duration, nor interdrink interval) also were not altered. There were no observable behavioral disruptions following CBD treatment. Conclusions: In sum, the current data do not support use of pure CBD as an effective pharmacotherapy to reduce ongoing excessive drinking.
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