Journal
NEUROBIOLOGY OF STRESS
Volume 20, Issue -, Pages -Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/j.ynstr.2022.100470
Keywords
Endocannabinoid; Stress; Stressor modality; Sex differences; Rats; Corticolimbic
Categories
Funding
- Canadian Institutes of Health Research (CIHR)
- CIHR (Vanier CGS) [FDN333950]
- University of Calgary (UofC)
- Alberta Innovates-Health Solutions (AIHS)
- Branch Out Neurological Foundation (BONF)
- AIHS
- CIHR
- CIHR (CGS-M)
- UofC (Mathison Centre Graduate Recruitment Scholarship in Mental Health and Cumming School of Medicine Graduate Scholarship)
- UofC (Mathison Centre Graduate Recruitment Scholarship in Mental Health)
- CIHR (CGS-D)
- AIHS
- Tier II Canada Research Chair in the Neurobiology of Stress
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Research has shown that the endocannabinoid system plays a role in the neural and endocrine responses to stress. This study investigated how the endocannabinoid levels change in response to different acute stress modalities in male rats. The results suggest that there are sex differences in the dynamic responses of endocannabinoids to stress. These findings contribute to our understanding of the interactions between stress and endocannabinoid function.
Research over the past few decades has established a role for the endocannabinoid system in contributing to the neural and endocrine responses to stress exposure. The two endocannabinoid ligands, anandamide (AEA) and 2-arachidonoyl glycerol (2-AG), both play roles in regulating the stress response and both exhibit dynamic changes in response to stress exposure. Most of this previous research, however, was conducted in male rodents. Given that, especially in rodents, the stress response is influenced by sex, an understanding of how these dynamic responses of endocannabinoids in response to stress is influenced by sex could provide insight into sex differences of the acute stress response. We exposed adult, Sprague Dawley rats to different commonly utilized acute stress modalities, specifically restraint, swim and foot shock stress. Thirty minutes following stress onset, we excised the amygdala, hippocampus and medial prefrontal cortex, corticolimbic brain regions involved in the stress response, to measure endocannabinoid levels. When AEA levels were altered in response to restraint and swim stress, they were reduced, whereas exposure to foot shock stress led to an increase in the amygdala. 2-AG levels, when they were altered by stress exposure were only increased, specifically in males in the amygdala following swim stress, and in the hippocampus and medial prefrontal cortex overall following foot shock stress. This in-crease in 2-AG levels following stress only in males was the only sex difference found in stress-induced changes in endocannabinoid levels. There were no consistent sex differences observed. Collectively, these data contribute to our further understanding of the interactions between stress and endocannabinoid function.
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