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Psychedelic-inspired approaches for treating neurodegenerative disorders.

Hannah N Saeger, David E Olson

Journal of neurochemistry July 1, 2022 Peer reviewed DOI: 10.1111/jnc.15544 via PubMed

Summary

Psychedelics may have therapeutic potential for neurodegenerative disorders by addressing cortical atrophy and influencing neurotrophic factor gene expression, neuronal growth, and immune modulation. Although their use has not yet been established in treating these diseases, psychedelics could help manage behavioral and psychological symptoms of dementia (BPSD) due to their effects on the 5-HT2A receptor, which is important for neuron health in Alzheimer's disease. Further research is necessary to explore these possibilities.

Study at a glance

Key finding Psychedelics might be useful for treating neurodegenerative diseases and managing BPSD due to their impact on neuroplasticity and inflammation.

Abstract

Psychedelics are increasingly being recognized for their potential to treat a wide range of brain disorders including depression, post-traumatic stress disorder (PTSD), and substance use disorder. Their broad therapeutic potential might result from an ability to rescue cortical atrophy common to many neuropsychiatric and neurodegenerative diseases by impacting neurotrophic factor gene expression, activating neuronal growth and survival mechanisms, and modulating the immune system. While the therapeutic potential of psychedelics has not yet been extended to neurodegenerative disorders, we provide evidence suggesting that approaches based on psychedelic science might prove useful for treating these diseases. The primary target of psychedelics, the 5-HT2A receptor, plays key roles in cortical neuron health and is dysregulated in Alzheimer's disease. Moreover, evidence suggests that psychedelics and related compounds could prove useful for treating the behavioral and psychological symptoms of dementia (BPSD). While more research is needed to probe the effects of psychedelics in models of neurodegenerative diseases, the robust effects of these compounds on structural and functional neuroplasticity and inflammation clearly warrant further investigation.

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