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D-cycloserine (DCS) is Not Susceptible to Self-administration, unlike S-ketamine Using an Intravenous Self-administration Model in Naive and Ketamine-habituated Sprague-Dawley Rats

Daniel C Javitt, Jonathan C. Javitt

bioRxiv Preprint Server August 12, 2022 preprint DOI: 10.1101/2022.08.12.503713 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Preclinical study
Population Ketamine-dependent rats
Interventions D-cycloserine ketamine
Topics Addiction Esketamine Ketamine
Keywords D-cycloserine Dcs Low abuse potential Non-addictive Addiction risk Drug dependence Dependence potential Substance abuse Antidepressants Antidepressant drugs Psychiatric medications Drug research Preclinical research Animal study Rat model Pharmacology Drug development
Key points D-cycloserine did not substitute for ketamine in a self-administration paradigm, indicating low abuse potential.

Abstract

OBJECTIVE N-methyl D-aspartate Receptor (NMDAR) antagonist antidepressants have known potential for abuse liability. The aim of this study was to evaluate the abuse liability of D-cycloserine (DCS), using a self-administration paradigm in which DCS was tested in its efficacy in substituting for ketamine in ketamine-dependent rats.

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