Literature DB >> 27569586

Endocannabinoids in brain plasticity: Cortical maturation, HPA axis function and behavior.

Diana Dow-Edwards1, Lindsay Silva2.   

Abstract

Marijuana use during adolescence has reached virtually every strata of society. The general population has the perception that marijuana use is safe for mature people and therefore is also safe for developing adolescents. However, both clinical and preclinical research shows that marijuana use, particularly prior to age 16, could have long-term effects on cognition, anxiety and stress-related behaviors, mood disorders and substance abuse. These effects derive from the role of the endocannabinoid system, the endogenous cannabinoid system, in the development of cortex, amygdala, hippocampus and hypothalamus during adolescence. Endocannabinoids are necessary for normal neuronal excitation and inhibition through actions at glutamate and GABA terminals. Synaptic pruning at excitatory synapses and sparing of inhibitory synapses likely results in changes in the balance of excitation/inhibition in individual neurons and within networks; processes which are necessary for normal cortical development. The interaction between prefrontal cortex (PFC), amygdala and hippocampus is responsible for emotional memory, anxiety-related behaviors and drug abuse and all utilize the endogenous cannabinoid system to maintain homeostasis. Also, endocannabinoids are required for fast and slow feedback in the normal stress response, processes which mature during adolescence. Therefore, exogenous cannabinoids, such as marijuana, have the potential to alter the course of development of each of these major systems (limbic, hypothalamic-pituitary-adrenal (HPA) axis and neocortex) if used during the critical period of brain development, adolescence. This article is part of a Special Issue entitled SI: Adolescent plasticity.
Copyright © 2016 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  HPA axis development; PFC prefrontal cortex; Pruning and endocannabinoids; Sex differences; Stress and CB receptors; Stress and CB responses

Mesh:

Substances:

Year:  2016        PMID: 27569586     DOI: 10.1016/j.brainres.2016.08.037

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  25 in total

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Journal:  Neuropsychopharmacology       Date:  2017-07-17       Impact factor: 7.853

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