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Cannabinoid Receptor 1 Is Required for Neurodevelopment of Striosome-Dendron Bouquets

Cannabinoid receptor 1 (CB1R) has strong effects on neurogenesis and axon pathfinding in the prenatal brain. Endocannabinoids that activate CB1R are abundant in the early postnatal brain and in mother’s milk, but few studies have investigated their function in newborns. We examined postnatal CB1R ex...

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Autores principales: Crittenden, Jill R., Yoshida, Tomoko, Venu, Samitha, Mahar, Ara, Graybiel, Ann M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9007419/
https://www.ncbi.nlm.nih.gov/pubmed/35361667
http://dx.doi.org/10.1523/ENEURO.0318-21.2022
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author Crittenden, Jill R.
Yoshida, Tomoko
Venu, Samitha
Mahar, Ara
Graybiel, Ann M.
author_facet Crittenden, Jill R.
Yoshida, Tomoko
Venu, Samitha
Mahar, Ara
Graybiel, Ann M.
author_sort Crittenden, Jill R.
collection PubMed
description Cannabinoid receptor 1 (CB1R) has strong effects on neurogenesis and axon pathfinding in the prenatal brain. Endocannabinoids that activate CB1R are abundant in the early postnatal brain and in mother’s milk, but few studies have investigated their function in newborns. We examined postnatal CB1R expression in the major striatonigral circuit from striosomes of the striatum to the dopamine-containing neurons of the substantia nigra. CB1R enrichment was first detectable between postnatal day (P)5 and P7, and this timing coincided with the formation of “striosome-dendron bouquets,” the elaborate anatomic structures by which striosomal neurons control dopaminergic cell activity through inhibitory synapses. In Cnr1(−/−) knock-out mice lacking CB1R expression, striosome-dendron bouquets were markedly disorganized by P11 and at adulthood, suggesting a postnatal pathfinding connectivity function for CB1R in connecting striosomal axons and dopaminergic neurons analogous to CB1R’s prenatal function in other brain regions. Our finding that CB1R plays a major role in postnatal wiring of the striatonigral dopamine-control system, with lasting consequences at least in mice, points to a crucial need to determine whether lactating mothers’ use of CB1R agonists (e.g., in marijuana) or antagonists (e.g., type 2 diabetes therapies) can disrupt brain development in nursing offspring.
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spelling pubmed-90074192022-04-14 Cannabinoid Receptor 1 Is Required for Neurodevelopment of Striosome-Dendron Bouquets Crittenden, Jill R. Yoshida, Tomoko Venu, Samitha Mahar, Ara Graybiel, Ann M. eNeuro Research Article: New Research Cannabinoid receptor 1 (CB1R) has strong effects on neurogenesis and axon pathfinding in the prenatal brain. Endocannabinoids that activate CB1R are abundant in the early postnatal brain and in mother’s milk, but few studies have investigated their function in newborns. We examined postnatal CB1R expression in the major striatonigral circuit from striosomes of the striatum to the dopamine-containing neurons of the substantia nigra. CB1R enrichment was first detectable between postnatal day (P)5 and P7, and this timing coincided with the formation of “striosome-dendron bouquets,” the elaborate anatomic structures by which striosomal neurons control dopaminergic cell activity through inhibitory synapses. In Cnr1(−/−) knock-out mice lacking CB1R expression, striosome-dendron bouquets were markedly disorganized by P11 and at adulthood, suggesting a postnatal pathfinding connectivity function for CB1R in connecting striosomal axons and dopaminergic neurons analogous to CB1R’s prenatal function in other brain regions. Our finding that CB1R plays a major role in postnatal wiring of the striatonigral dopamine-control system, with lasting consequences at least in mice, points to a crucial need to determine whether lactating mothers’ use of CB1R agonists (e.g., in marijuana) or antagonists (e.g., type 2 diabetes therapies) can disrupt brain development in nursing offspring. Society for Neuroscience 2022-04-08 /pmc/articles/PMC9007419/ /pubmed/35361667 http://dx.doi.org/10.1523/ENEURO.0318-21.2022 Text en Copyright © 2022 Crittenden et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article: New Research
Crittenden, Jill R.
Yoshida, Tomoko
Venu, Samitha
Mahar, Ara
Graybiel, Ann M.
Cannabinoid Receptor 1 Is Required for Neurodevelopment of Striosome-Dendron Bouquets
title Cannabinoid Receptor 1 Is Required for Neurodevelopment of Striosome-Dendron Bouquets
title_full Cannabinoid Receptor 1 Is Required for Neurodevelopment of Striosome-Dendron Bouquets
title_fullStr Cannabinoid Receptor 1 Is Required for Neurodevelopment of Striosome-Dendron Bouquets
title_full_unstemmed Cannabinoid Receptor 1 Is Required for Neurodevelopment of Striosome-Dendron Bouquets
title_short Cannabinoid Receptor 1 Is Required for Neurodevelopment of Striosome-Dendron Bouquets
title_sort cannabinoid receptor 1 is required for neurodevelopment of striosome-dendron bouquets
topic Research Article: New Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9007419/
https://www.ncbi.nlm.nih.gov/pubmed/35361667
http://dx.doi.org/10.1523/ENEURO.0318-21.2022
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