Cannabinoid use generalizes stress responses by altering the astrocyte plasticity through extracellular matrix signaling in the nucleus accumbens core.
Ritchy Hodebourg, Lillian Duncan, Eric Dereschewitz, Peter Kalivas
Research square August 21, 2025 DOI: 10.21203/rs.3.rs-7254957/v1 via PubMed
Summary
AI-generated from the abstractCannabinoid use after stress causes male rats to generalize fear responses to neutral cues and adopt avoidant coping behaviors. The combination of THC and CBD triggered distinct brain changes in the nucleus accumbens core: astrocytes retracted from synapses and Synapsin-I density decreased when a neutral odor was presented, while exposure to a stress-conditioned odor activated MMP-2,9 (mostly MMP-2), re-associated astrocytes to synapses, increased Synapsin-I density, and caused astrocyte atrophy. These neuroadaptations occurred only in males. The findings suggest MMPs and astrocytes as potential therapeutic targets for co-occurring cannabis use disorder and PTSD.
Study at a glance
| Characteristics | Animal study Peer reviewed |
|---|---|
| Population | Male and female rats |
| Duration | 10 days of self-administration followed by 10 days of withdrawal |
| Key finding | THC + CBD generalized stress responses to a neutral stimulus and promoted avoidant coping behaviors in male rats through distinct astroglial and synaptic plasticity changes in the nucleus accumbens core. |
Abstract
The rising legal acceptance of cannabis and the high comorbidity between cannabis use disorder (CUD) and post-traumatic stress disorder (PTSD) highlight the importance of understanding how stress and cannabis influence the brain. We recently discovered that cannabis use promotes two PTSD-like symptoms: avoidance coping behaviors and the generalization of stress-coping responses to a neutral stimulus not previously linked to stress. To investigate the neuroadaptations behind these changes, we used in vivo zymography and confocal microscopy to examine how stress and cannabinoid use influence multipartite synaptic plasticity in the nucleus accumbens core (NAcore), including astroglial plasticity, Synapsin-I density, and matrix metalloproteinases (MMP-2,9) activity. For this purpose, rats were restraint stressed for 2h and simultaneously exposed to an odor that became the stress-conditioned stimulus (stress-CS). Three weeks later, rats self-administered cannabinoids (delta9-tetrahydrocannabinol + cannabidiol; THC + CBD) for 10 days, followed by 10 days of withdrawal. We then evaluated the effect of stress-CS or neutral odor (NS) on coping strategies in a defensive burying task. We demonstrated for the first time that THC + CBD generalized stress responses to the NS by causing astrocytes to retract from synapses and decreasing Synapsin-I density in the NAcore. Furthermore, cannabinoid use promoted avoidant coping behaviors in response to a stress-CS by triggering strong activation of MMP-2,9, driven largely by MMP-2, causing a re-association of astrocytes to synapses along with an increase of Synapsin-I density and astrocyte atrophy. However, these neuroadaptations only occurred in males. Overall, these findings highlight potential therapeutic targets like MMPs and astrocytes for treating co-occurring CUD/PTSD.