Ketone Supplementation Dampens Subjective and Objective Responses to Alcohol: Evidence From a Preclinical Rat Study and a Randomized, Cross-Over Trial in Healthy Volunteers

Author:

Li Xinyi1ORCID,Shi Zhenhao1,Todaro Dustin R1,Pond Timothy1,Byanyima Juliana I1,Vesslee Sianneh A1,Reddy Rishika1,Nanga Ravi Prakash Reddy2,Kass Gabriel1,Ramchandani Vijay3,Kranzler Henry R1ORCID,Vendruscolo Janaina C M4,Vendruscolo Leandro F4,Wiers Corinde E1ORCID

Affiliation:

1. Center for Studies of Addiction, Department of Psychiatry, University of Pennsylvania Perelman School of Medicine , Philadelphia, Pennsylvania , USA

2. University of Pennsylvania Perelman School of Medicine, Department of Radiology , Philadelphia, Pennsylvania , USA

3. National Institute on Alcohol Abuse and Alcoholism , National Institutes of Health, Bethesda, Maryland , USA

4. National Institute on Drug Abuse, National Institutes of Health , Baltimore, Maryland , USA

Abstract

Abstract Background Previous preclinical and human studies have shown that a high-fat ketogenic diet and ketone supplements (KS) are efficacious in reducing alcohol craving, alcohol consumption, and signs of alcohol withdrawal. However, the effects of KS on alcohol sensitivity are unknown. Methods In this single-blind, cross-over study, 10 healthy participants (3 females) were administered a single, oral dose of a KS (25 g of ketones from D-β-hydroxybutyric acid and R-1,3-butanediol) or placebo 30 minutes before an oral alcohol dose (0.25 g/kg for women; 0.31 g/kg for men). Assessments of breath alcohol concentration and blood alcohol levels (BAL) and responses on the Drug Effect Questionnaire were repeatedly obtained over 180 minutes after alcohol consumption. In a parallel preclinical study, 8 Wistar rats (4 females) received an oral gavage of KS (0.42 g ketones/kg), water, or the sweetener allulose (0.58 g/kg) followed 15 minutes later by an oral alcohol dose (0.8 g/kg). BAL was monitored for 240 minutes after alcohol exposure. Results In humans, the intake of KS before alcohol significantly blunted breath alcohol concentration and BAL, reduced ratings of alcohol liking and wanting more, and increased disliking for alcohol. In rats, KS reduced BAL more than either allulose or water. Conclusion KS altered physiological and subjective responses to alcohol in both humans and rats, and the effects were likely not mediated by the sweetener allulose present in the KS drink. Therefore, KS could potentially reduce the intoxicating effects of alcohol.

Funder

National Institutes of Health

Publisher

Oxford University Press (OUP)

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