Early life stress and development of the endocannabinoid system: A bidirectional process in programming future coping

The endocannabinoid system (ECS) critically regulates stress responsivity and emotional behavior throughout development. It regulates anxiety-like behaviors in humans and animal models. In addition, it is sensitive to early life stress at the gene expression level in a sex-dependent and region-dependent manner, and these changes are already evident in the adolescent brain. The ECS modulates the neuroendocrine and behavioral effects of stress, and is also capable of being affected by stress exposure itself. Early life stress interferes with the development of corticolimbic circuits, a major location of endocannabinoid receptors, and increases vulnerability to adult psychopathology. Early life stress alters the ontogeny of the ECS, resulting in a sustained deficit in its function, particularly within the hippocampus. Specifically, exposure to early stress results in bidirectional changes in anandamide and 2-AG tissue levels within the amygdala and hippocampus and reduces hippocampal endocannabinoid function at puberty. CB1 receptor densities across all brain regions are downregulated later in life following exposure to early life stress. Manipulations affecting the glucocorticoid and the endocannabinoid systems persistently adjust individual emotional responses and synaptic plasticity. This review aims to show the bidirectional trajectories of endocannabinoid modulation of emotionality in reaction to early life stress.

Automated summary

The endocannabinoid system plays a critical role in regulating anxiety-like behaviors in humans and animal models, with early life stress potentially impacting gene expression and leading to changes in the adolescent brain. It modulates the neuroendocrine and behavioral effects of stress, while being sensitive to stress exposure itself, potentially increasing vulnerability to adult psychopathology. Early life stress alters the ontogeny of the ECS and can result in bidirectional changes in tissue levels of specific endocannabinoids in brain regions like the amygdala and hippocampus.