Dopamine-receptor blocking agent-associated akathisia: a summary of current understanding and proposal for a rational approach to treatment

Dopamine-receptor blocking agent-associated akathisia (DRBA-A) is an adverse effect that can significantly limit the use of these important medications for the treatment of a variety of psychiatric diseases, yet there is no unifying theory regarding its pathophysiology. This knowledge gap limits cli...

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Main Authors: Shaina Musco, Vivian McAllister, Ian Caudle
Format: Article
Language:English
Published: SAGE Publishing 2020-08-01
Series:Therapeutic Advances in Psychopharmacology
Online Access:https://doi.org/10.1177/2045125320937575
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spelling doaj-8692746a7ff84fd0a19c3ef94f0d3d7a2020-11-25T03:44:01ZengSAGE PublishingTherapeutic Advances in Psychopharmacology2045-12612020-08-011010.1177/2045125320937575Dopamine-receptor blocking agent-associated akathisia: a summary of current understanding and proposal for a rational approach to treatmentShaina MuscoVivian McAllisterIan CaudleDopamine-receptor blocking agent-associated akathisia (DRBA-A) is an adverse effect that can significantly limit the use of these important medications for the treatment of a variety of psychiatric diseases, yet there is no unifying theory regarding its pathophysiology. This knowledge gap limits clinicians’ ability to effectively manage DRBA-A and mitigate negative outcomes in an already vulnerable patient population. Based on a review of the current literature on the subject, it is hypothesized that dopaminergic and noradrenergic signaling is perturbed in DRBA-A. Accordingly, it is proposed that the optimal agent to manage this extrapyramidal symptom should increase dopamine signaling in the affected areas of the brain and counteract compensatory noradrenergic signaling via antagonism of adrenergic or serotonergic receptors.https://doi.org/10.1177/2045125320937575
collection DOAJ
language English
format Article
sources DOAJ
author Shaina Musco
Vivian McAllister
Ian Caudle
spellingShingle Shaina Musco
Vivian McAllister
Ian Caudle
Dopamine-receptor blocking agent-associated akathisia: a summary of current understanding and proposal for a rational approach to treatment
Therapeutic Advances in Psychopharmacology
author_facet Shaina Musco
Vivian McAllister
Ian Caudle
author_sort Shaina Musco
title Dopamine-receptor blocking agent-associated akathisia: a summary of current understanding and proposal for a rational approach to treatment
title_short Dopamine-receptor blocking agent-associated akathisia: a summary of current understanding and proposal for a rational approach to treatment
title_full Dopamine-receptor blocking agent-associated akathisia: a summary of current understanding and proposal for a rational approach to treatment
title_fullStr Dopamine-receptor blocking agent-associated akathisia: a summary of current understanding and proposal for a rational approach to treatment
title_full_unstemmed Dopamine-receptor blocking agent-associated akathisia: a summary of current understanding and proposal for a rational approach to treatment
title_sort dopamine-receptor blocking agent-associated akathisia: a summary of current understanding and proposal for a rational approach to treatment
publisher SAGE Publishing
series Therapeutic Advances in Psychopharmacology
issn 2045-1261
publishDate 2020-08-01
description Dopamine-receptor blocking agent-associated akathisia (DRBA-A) is an adverse effect that can significantly limit the use of these important medications for the treatment of a variety of psychiatric diseases, yet there is no unifying theory regarding its pathophysiology. This knowledge gap limits clinicians’ ability to effectively manage DRBA-A and mitigate negative outcomes in an already vulnerable patient population. Based on a review of the current literature on the subject, it is hypothesized that dopaminergic and noradrenergic signaling is perturbed in DRBA-A. Accordingly, it is proposed that the optimal agent to manage this extrapyramidal symptom should increase dopamine signaling in the affected areas of the brain and counteract compensatory noradrenergic signaling via antagonism of adrenergic or serotonergic receptors.
url https://doi.org/10.1177/2045125320937575
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