A mechanistic overview of approaches for the treatment of psychostimulant dependence

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Psychostimulant use disorder is a major health issue around the world with enormous individual, family-related and societal consequences, yet there are no effective pharmacological treatments available. In this review, a target-based overview of pharmacological treatments toward psychostimulant addiction will be presented. We will go through therapeutic approaches targeting different aspects of psychostimulant addiction with focus on three major areas; 1) drugs targeting signalling, and metabolism of the dopamine system, 2) drugs targeting either AMPA receptors or metabotropic glutamate receptors of the glutamate system and 3) drugs targeting the severe side-effects of quitting long-term psychostimulant use. For each of these major modes of intervention, findings from pre-clinical studies in rodents to clinical trials in humans will be listed, and future perspectives of the different treatment strategies as well as their potential side-effects will be discussed. Pharmaceuticals modulating the dopamine system, such as antipsychotics, DAT-inhibitors, and disulfiram, have shown some promising results. Cognitive enhancers have been found to increase aspects of behavioural control, and drugs targeting the glutamate system such as modulators of metabotropic glutamate receptors and AMPA receptors have provided interesting changes in relapse behaviour. Furthermore, CRF-antagonists directed toward alleviating the symptoms of the withdrawal stage have been examined with interesting resulting changes in behaviour. There are promising results investigating therapeutics for psychostimulant addiction, but further preclinical work and additional human studies with a more stratified patient selection are needed to prove sufficient evidence of efficacy and tolerability.

OriginalsprogEngelsk
Artikelnummer854176
TidsskriftFrontiers in Pharmacology
Vol/bind13
Antal sider22
ISSN1663-9812
DOI
StatusUdgivet - 2022

Bibliografisk note

Funding Information:
This work was supported by Lundbeck Foundation R322-2019-1816 (KJ); NOVO Seed, Dolorest NNF19SA0055737 (KM); NOVO Nordisk, NNF21OC0070287 (KM); NOVO Nordisk NNF20OC0065309 (KM), and Lundbeck Foundation R344-2020-1063 (KM).

Publisher Copyright:
Copyright © 2022 Jensen, Jensen and Madsen.

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