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Effects of psychedelics on neurogenesis and broader neuroplasticity : a systematic review

Lima da Cruz, Rafael V. ; Leão, Richardson N. and Moulin, Thiago C. LU (2024) In Molecular Medicine 30(1).
Abstract

In the mammalian brain, new neurons continue to be generated throughout life in a process known as adult neurogenesis. The role of adult-generated neurons has been broadly studied across laboratories, and mounting evidence suggests a strong link to the HPA axis and concomitant dysregulations in patients diagnosed with mood disorders. Psychedelic compounds, such as phenethylamines, tryptamines, cannabinoids, and a variety of ever-growing chemical categories, have emerged as therapeutic options for neuropsychiatric disorders, while numerous reports link their effects to increased adult neurogenesis. In this systematic review, we examine studies assessing neurogenesis or other neurogenesis-associated brain plasticity after psychedelic... (More)

In the mammalian brain, new neurons continue to be generated throughout life in a process known as adult neurogenesis. The role of adult-generated neurons has been broadly studied across laboratories, and mounting evidence suggests a strong link to the HPA axis and concomitant dysregulations in patients diagnosed with mood disorders. Psychedelic compounds, such as phenethylamines, tryptamines, cannabinoids, and a variety of ever-growing chemical categories, have emerged as therapeutic options for neuropsychiatric disorders, while numerous reports link their effects to increased adult neurogenesis. In this systematic review, we examine studies assessing neurogenesis or other neurogenesis-associated brain plasticity after psychedelic interventions and aim to provide a comprehensive picture of how this vast category of compounds regulates the generation of new neurons. We conducted a literature search on PubMed and Science Direct databases, considering all articles published until January 31, 2023, and selected articles containing both the words “neurogenesis” and “psychedelics”. We analyzed experimental studies using either in vivo or in vitro models, employing classical or atypical psychedelics at all ontogenetic windows, as well as human studies referring to neurogenesis-associated plasticity. Our findings were divided into five main categories of psychedelics: CB1 agonists, NMDA antagonists, harmala alkaloids, tryptamines, and entactogens. We described the outcomes of neurogenesis assessments and investigated related results on the effects of psychedelics on brain plasticity and behavior within our sample. In summary, this review presents an extensive study into how different psychedelics may affect the birth of new neurons and other brain-related processes. Such knowledge may be valuable for future research on novel therapeutic strategies for neuropsychiatric disorders.

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Please use this url to cite or link to this publication:
author
; and
organization
publishing date
type
Contribution to journal
publication status
published
subject
keywords
Dentate gyrus, Hallucinogens, Major depression, Neurogenesis, Plasticity, Psychedelics
in
Molecular Medicine
volume
30
issue
1
article number
244
publisher
The Feinstein Institute for Medical Research
external identifiers
  • pmid:39701927
  • scopus:85212397764
ISSN
1076-1551
DOI
10.1186/s10020-024-01013-4
language
English
LU publication?
yes
id
714b6ea4-27d9-446d-8870-10e63f533143
date added to LUP
2025-01-17 11:58:49
date last changed
2025-06-06 23:15:01
@article{714b6ea4-27d9-446d-8870-10e63f533143,
  abstract     = {{<p>In the mammalian brain, new neurons continue to be generated throughout life in a process known as adult neurogenesis. The role of adult-generated neurons has been broadly studied across laboratories, and mounting evidence suggests a strong link to the HPA axis and concomitant dysregulations in patients diagnosed with mood disorders. Psychedelic compounds, such as phenethylamines, tryptamines, cannabinoids, and a variety of ever-growing chemical categories, have emerged as therapeutic options for neuropsychiatric disorders, while numerous reports link their effects to increased adult neurogenesis. In this systematic review, we examine studies assessing neurogenesis or other neurogenesis-associated brain plasticity after psychedelic interventions and aim to provide a comprehensive picture of how this vast category of compounds regulates the generation of new neurons. We conducted a literature search on PubMed and Science Direct databases, considering all articles published until January 31, 2023, and selected articles containing both the words “neurogenesis” and “psychedelics”. We analyzed experimental studies using either in vivo or in vitro models, employing classical or atypical psychedelics at all ontogenetic windows, as well as human studies referring to neurogenesis-associated plasticity. Our findings were divided into five main categories of psychedelics: CB1 agonists, NMDA antagonists, harmala alkaloids, tryptamines, and entactogens. We described the outcomes of neurogenesis assessments and investigated related results on the effects of psychedelics on brain plasticity and behavior within our sample. In summary, this review presents an extensive study into how different psychedelics may affect the birth of new neurons and other brain-related processes. Such knowledge may be valuable for future research on novel therapeutic strategies for neuropsychiatric disorders.</p>}},
  author       = {{Lima da Cruz, Rafael V. and Leão, Richardson N. and Moulin, Thiago C.}},
  issn         = {{1076-1551}},
  keywords     = {{Dentate gyrus; Hallucinogens; Major depression; Neurogenesis; Plasticity; Psychedelics}},
  language     = {{eng}},
  number       = {{1}},
  publisher    = {{The Feinstein Institute for Medical Research}},
  series       = {{Molecular Medicine}},
  title        = {{Effects of psychedelics on neurogenesis and broader neuroplasticity : a systematic review}},
  url          = {{http://dx.doi.org/10.1186/s10020-024-01013-4}},
  doi          = {{10.1186/s10020-024-01013-4}},
  volume       = {{30}},
  year         = {{2024}},
}