Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2025 May;398(5):5057-5075.
doi: 10.1007/s00210-024-03757-6. Epub 2024 Dec 30.

Trace amine-associated receptor 1 (TAAR1): an emerging therapeutic target for neurodegenerative, neurodevelopmental, and neurotraumatic disorders

Affiliations
Review

Trace amine-associated receptor 1 (TAAR1): an emerging therapeutic target for neurodegenerative, neurodevelopmental, and neurotraumatic disorders

Saher Dalvi et al. Naunyn Schmiedebergs Arch Pharmacol. 2025 May.

Abstract

Trace amines are physiologically active amines present in all organisms. They are structurally identical to traditional monoamines and are rapidly metabolized by monoamine oxidases. The mammalian neurological system generates these molecules at rates equivalent to traditional monoamines, but because of their short half-life, they are only observable in trace quantities. Their receptors are G protein-coupled receptors present in both the CNS and peripheral locations, with trace amine-associated receptor 1 (TAAR1) being the most researched. TAAR1's capacity to regulate glutamatergic and monoaminergic neurotransmission has made it a viable therapeutic target for neuropsychiatric illnesses. Although the TAAR1 role in schizophrenia and other neuropsychiatric disorders is well established, its role in the pathology of neurodegenerative and neurotraumatic disorders recently got attention. This review discusses the role of TAAR1 in neurodegenerative, neurodevelopment, and neurotraumatic disorders and explores its potential to be a novel therapeutic target in these disorders.

Keywords: Neurodegenerative disease; Neurotraumatic disorders; TAAR1; Trace amine-associated receptors; Trace amines.

PubMed Disclaimer

Conflict of interest statement

Declarations. Ethics approval and consent to participate: Not applicable Consent for publication: Not applicable Competing interests: The authors declare no competing interests.

Similar articles

References

    1. Accorroni A, Rutigliano G, Sabatini M et al (2020) Exogenous 3-iodothyronamine rescues the entorhinal cortex from β-amyloid toxicity. Thyroid 30:147–160. https://doi.org/10.1089/thy.2019.0255 - DOI - PubMed
    1. Achat-Mendes C, Lynch LJ, Sullivan KA et al (2012) Augmentation of methamphetamine-induced behaviors in transgenic mice lacking the trace amine-associated receptor 1. Pharmacol Biochem Behav 101:201–207. https://doi.org/10.1016/j.pbb.2011.10.025 - DOI - PubMed
    1. Ågren R, Betari N, Saarinen M et al (2023) In vitro comparison of ulotaront (SEP-363856) and ralmitaront (RO6889450): two TAAR1 agonist candidate antipsychotics. Int J Neuropsychopharmacol 26:599–606. https://doi.org/10.1093/ijnp/pyad049 - DOI - PubMed - PMC
    1. Ahuja CS, Nori S, Tetreault L et al (2017) Traumatic spinal cord injury-repair and regeneration. Neurosurgery 80:S9–S22. https://doi.org/10.1093/neuros/nyw080 - DOI - PubMed
    1. Alizadeh A, Dyck SM, Karimi-Abdolrezaee S (2019) Traumatic spinal cord injury: an overview of pathophysiology, models and acute injury mechanisms. Front Neurol 10:282. https://doi.org/10.3389/fneur.2019.00282 - DOI - PubMed - PMC

MeSH terms

Substances

LinkOut - more resources