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Review
. 2025 Sep 3.
doi: 10.1007/s40261-025-01473-4. Online ahead of print.

Revisiting the Role of Serotonin in Attention-Deficit Hyperactivity Disorder: New Insights from Preclinical and Clinical Studies

Affiliations
Review

Revisiting the Role of Serotonin in Attention-Deficit Hyperactivity Disorder: New Insights from Preclinical and Clinical Studies

Matia B Solomon et al. Clin Drug Investig. .

Abstract

Attention-deficit hyperactivity disorder (ADHD) is characterized by core symptoms of inattention, hyperactivity, and impulsivity. Aberrant dopaminergic and noradrenergic neurotransmission are often implicated in the pathogenesis of these symptoms because ADHD treatments increase synaptic levels of these neurotransmitters in brain regions associated with attention and impulse control. However, some ADHD treatments also enhance serotonergic neurotransmission in these regions, which could contribute to their efficacy. Here, we review preclinical and clinical data highlighting functional interactions between the serotonergic and catecholaminergic systems in mediating ADHD phenotypes and responses to treatment. The potential utility of serotonergic compounds for treating distinct behavioral features and psychiatric comorbidities (e.g., depression) is also discussed. Overall, preclinical and clinical studies underscore important neuromodulatory effects of serotonin on the catecholaminergic system in mediating distinct ADHD behavioral phenotypes, notably hyperactivity-impulsivity and emotional dysregulation. Incorporating a basic understanding of dynamic monoaminergic interactions and their contributions to ADHD symptoms may identify new targets for treatment. Beyond ADHD core symptoms, emotional dysregulation, which is closely linked to serotonergic dysfunction, is common in ADHD and significantly contributes to negative outcomes across the lifespan. Therefore, an expanded conceptualization of ADHD that includes emotional dysregulation may facilitate insight into ADHD pathology and treatment.

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Conflict of interest statement

Declarations. Conflict of interest: M.B.S. was formerly employed by Supernus Pharmaceuticals Inc. B.Y. and J.R. are currently employed by Supernus Pharmaceuticals Inc. T.R., J.N., and V.M. are consultants and/or advisory board members for Supernus Pharmaceuticals Inc. J.N. is also a consultant for Hippo T&C, Lumos, MindTension, NFL, and OnDosis; an advisory board member for Medice, Mind Tension, OnDosis, Otsuka; and receives research support from Otsuka. V.M. is also a consultant for AbbVie/Allergan, Acadia Pharmaceuticals, Inc. Alfasigma, USA, Inc., AlkernesInc., Axsome, Eisai, Ironshore, Intra-Cellular Therapies, Janssen, H. Lundbeck A/S, Jazz Pharmaceuticals, NovenPharmaceuticals Inc., Otsuka America Pharmaceutical, Inc., Sage Pharmaceuticals, Sunovion Pharmaceuticals, and Takeda Pharmaceutical Company Limited. T.R. is also a consultant with Cambridge Cognition, has a research grant with Shionogi, and receives editorial honoraria from Springer-Nature and Elsevier. Ethics approval: Not applicable. Consent to participate: Not applicable. Consent for publication: Not applicable. Availability of data and material: Not applicable. Code availability: Not applicable. Author contributions: J.R., M.B.S., and B.Y. conceptualized and designed the review. M.B.S., B.Y., and T.W.R. conducted the literature search. M.B.S., B.Y., T.W.R., and V.M. drafted the initial manuscript. V.M. was not able to review or approve the final version of the manuscript, as he sadly passed away prior to the revision stage. His inclusion as a co-author was approved by his family in recognition of his contributions to the original submission. All remaining authors critically reviewed the manuscript, read and approved the final submitted manuscript, and agree to be accountable for the work.

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