4.3 Article

Physiological Rules of Endocannabinoid Action During Fetal and Neonatal Brain Development

期刊

CANNABIS AND CANNABINOID RESEARCH
卷 6, 期 5, 页码 381-388

出版社

MARY ANN LIEBERT, INC
DOI: 10.1089/can.2021.0096

关键词

axon guidance; cell fate; corticogenesis; neurogenesis; synapse

资金

  1. Swedish Research Council
  2. Novo Nordisk Foundation
  3. Hjarnfonden
  4. European Research Council (SECRET-CELLS) [ERC-2015-AdG-695136]

向作者/读者索取更多资源

The endocannabinoid system plays a key role in neurodevelopment by regulating neurogenic events that determine the number, placement, and connectivity of neurons. The use of plant-derived cannabinoids may interfere with the endocannabinoid system's regulatory functions, leading to developmental errors and impacting the ability of neural circuits. Maternal cannabis use during pregnancy may result in lifelong psychiatric phenotypes in offspring.
The endocannabinoid system is chiefly recognized as a homeostatic regulator of synaptic neurotransmission, primarily through the modulation of presynaptic CB1 cannabinoid neurons. Accordingly, the use of plant-derived cannabinoids received significant attention recently given the broad spectrum of physiological and pathobiological processes the endocannabinoid system is involved in. Nevertheless, a parallel line of research from a number of developmental biology groups has uncovered fundamental, evolutionarily conserved, and molecularly unique processes that endocannabinoids drive during development of the central nervous system. This lecture transcript is a concise summary of nearly 20 years of research on endocannabinoid-gated mechanisms of neurogenic specification events, which particularly define the numbers, placement, and connectivity of cortical neurons. A summary of both CB1 and alternative cannabinoid receptor contributions to neural differentiation is also discussed. Besides, insights are given into how phytocannabinoids can bypass physiologically timed and pivoted endocannabinoid action to inflict developmental errors that can significantly compromise the adaptive and computational ability of neurocircuits. By discussing specific subcellular targets of phytocannabinoid action and inferring errant glia versus neuron fate decisions and communication, a cellular basis is outlined for lifelong psychiatric phenotypes in offspring that associate with maternal cannabis seeking during pregnancy.

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