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2-Fluorodeschloroketamine has similar abuse potential as ketamine.

Feng Li, Han Du, Bo Wu, Jiayun Wei, Yanling Qiao, Miaojun Lai, Wenhua Zhou, Haowei Shen, Youmei Wang, Peng Xu, Bin Di

Addiction biology May 1, 2022 DOI: 10.1111/adb.13171 via PubMed

Summary

AI-generated from the abstract

The drug 2-fluorodeschloroketamine (2-FDCK), a ketamine substitute used by drug abusers, shows abuse potential comparable to ketamine. In mice, 2-FDCK at 3 mg/kg induced conditioned place preference, similar to ketamine. Acute injections at 30 mg/kg increased locomotor activity, and repeated treatments led to locomotor sensitization after withdrawal. 2-FDCK supported self-administration at 0.5 mg/kg/infusion, matching ketamine, with peak seeking at 1 mg/kg. In drug discrimination tests, 2-FDCK dose-dependently substituted for ketamine with comparable potency. These findings indicate that 2-FDCK has an abuse potential similar to ketamine.

Study at a glance

Characteristics Preclinical experimental study Peer reviewed
Population Mice
Interventions 2-FDCK ketamine
Dose 3 mg/kg, 30 mg/kg, 0.5 mg/kg/infusion, 1 mg/kg
Topics Ketamine
Keywords 2-fluorodeschloroketamine Conditioned place preference Drug discrimination Drug self-administration Locomotor sensitization
Citations 16
Key finding 2-FDCK has an abuse potential comparable to ketamine across multiple behavioral tests in mice.

Abstract

2-Fluorodeschloroketamine (2-FDCK) as a substitute for ketamine has emerged among drug abusers in recent years. However, 2-FDCK has not been controlled or regulated in many countries, which may be partly related to the lack of evidence on its abuse potential. In this study, we evaluated the abuse potential of 2-FDCK via the tests of the conditioned place preference (CPP), locomotor sensitization, drug self-administration and drug discrimination using ketamine as a reference. 2-FDCK induced significant CPP at a minimum dose of 3 mg/kg in mice, an effect comparable with that of ketamine (3 mg/kg). Acute injections of 2-FDCK or ketamine at 30 mg/kg enhanced locomotor activity. Repeated treatments with this dose of 2-FDCK and ketamine induced locomotor sensitization after withdrawal. 2-FDCK readily induced self-administration with 0.5 mg/kg/infusion, the same dose for ketamine, and induced the highest seeking response at 1 mg/kg. Drug discrimination test showed that 2-FDCK dose-dependently substitute for ketamine with comparable ED50 to ketamine in substitution testing. Taken together, these results strongly suggested that 2-FDCK has an abuse potential comparable with ketamine.

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