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The protective effect of DMT against neurodegeneration.

Ede Frecska, Attila Kovács, Attila Szabo

International review of neurobiology 2025 DOI: 10.1016/bs.irn.2025.04.010 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Review Peer reviewed
Intervention DMT
Topics DMT Serotonin
Keywords Alzheimer’s disease Amyotrophic lateral sclerosis Brain ischemia Neurodegenerative disorders Sigma-1 receptor Stroke Neuroprotection neuroprotection Protect the brain Mitigate ischemia-reperfusion injury Dimethyltryptamine dimethyltryptamine
Citations 2
Key findings DMT may have therapeutic potential for neuroprotection against ischemia-reperfusion injury and neurodegenerative disorders through its action on sigma-1 and serotonin receptors.

Abstract

This paper explores the therapeutic potential of DMT in neuroprotective strategies, particularly concerning ischemia-reperfusion injury (IRI) and neurodegenerative disorders. Besides its potent serotonin receptor actions, DMT is also an endogenous agonist of the sigma-1 receptor (Sig-1R). Sigma receptors are a unique family of proteins with high expression in the brain and spinal cord and have been involved in the etiology, symptom course and treatment of several central nervous system disorders. Our previous theoretical and experimental work strongly suggest that targeting sigma (and serotonin) receptors via DMT may be particularly useful for treatment in a number of neurological conditions like stroke, global brain ischemia, Alzheimer's disease, and amyotrophic lateral sclerosis. In this article, we briefly overview the function of Sig1-R in cellular bioenergetics with a focus on the processes involved in IRI and summarize the results of our previous preclinical (in vitro and in vivo) DMT studies aiming at mitigating IRI and related cellular neuropathologies. We conclude that the effect of DMT may involve a universal role in cellular protective mechanisms suggesting therapeutic potentials against different components and types of IRIs emerging in local and generalized brain ischemia after stroke or cardiac arrest. The multiple neuroprotective mechanisms facilitated by DMT may position it as a model molecule for developing pharmacological treatments for neurodegenerative disorders.

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