PDE4 inhibitor drug apremilast decreases alcohol intake
Pre-clinical and clinical evidence for suppression of alcohol intake by
apremilast
Treatment options for Alcohol Use Disorders (AUD) have minimally
advanced since 2004, while the annual deaths and economic toll have increased
alarmingly. Phosphodiesterase type 4 (PDE4) is associated with alcohol and
nicotine dependence. PDE4 inhibitors were identified as a potential AUD
treatment using a novel bioinformatics approach. We prioritized a newer PDE4
inhibitor, apremilast, as ideal for repurposing, (i.e. FDA approved for
psoriasis, low incidence of adverse events, excellent safety profile), and
tested it using multiple animal strains and models, as well as in a human Phase
IIa study. We found that apremilast reduced binge-like alcohol intake and
behavioral measures of alcohol motivation in mouse models of genetic risk for
drinking to intoxication. Apremilast also reduced excessive alcohol drinking in
models for stress-facilitated drinking and alcohol dependence. Using
site-directed drug infusions and electrophysiology, we uncovered that apremilast
may act to lessen drinking in mice by increasing neural activity in the nucleus
accumbens, a key brain region in the regulation of alcohol intake. Importantly,
apremilast (90 mg/d) reduced excessive drinking in non-treatment seeking
individuals with AUD in a double blind, placebo-controlled study. These results
demonstrate that apremilast suppresses excessive alcohol drinking across the
spectrum of AUD severity.
https://www.jci.org/articles/view/159103