Journal
MOLECULAR NEUROBIOLOGY
Volume 59, Issue 3, Pages 1896-1911Publisher
SPRINGER
DOI: 10.1007/s12035-022-02722-9
Keywords
Cannabinoid; Gene expression; Reward; Addiction; Epigenetic
Categories
Funding
- Universite de Strasbourg, Centre National de la Recherche Scientifique (CNRS), Programme International de Cooperation Scientifique (PICS CNRS)
- Natural Sciences and Engineering Research Council of Canada (NSERC)
- Agence Nationale de la Recherche [ANR-2017-CE12-0027]
- French Ministere de l'Enseignement Superieur et de la Recherche
- Fonds Paul Mandel
- IdEx Fellowship Program (Universite de Strasbourg)
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This study investigated the long-term adaptations induced by cocaine self-administration, including transcriptional modifications and associated epigenetic processes. The results suggest that the endogenous cannabinoid system may play a role in this process, and highlight the key role of the hippocampus in cocaine-induced plasticity.
Cocaine addiction is a complex pathology inducing long-term neuroplastic changes that, in turn, contribute to maladaptive behaviors. This behavioral dysregulation is associated with transcriptional reprogramming in brain reward circuitry, although the mechanisms underlying this modulation remain poorly understood. The endogenous cannabinoid system may play a role in this process in that cannabinoid mechanisms modulate drug reward and contribute to cocaine-induced neural adaptations. In this study, we investigated whether cocaine self-administration induces long-term adaptations, including transcriptional modifications and associated epigenetic processes. We first examined endocannabinoid gene expression in reward-related brain regions of the rat following self-administered (0.33 mg/kg intravenous, FR1, 10 days) cocaine injections. Interestingly, we found increased Cnr1 expression in several structures, including prefrontal cortex, nucleus accumbens, dorsal striatum, hippocampus, habenula, amygdala, lateral hypothalamus, ventral tegmental area, and rostromedial tegmental nucleus, with most pronounced effects in the hippocampus. Endocannabinoid levels, measured by mass spectrometry, were also altered in this structure. Chromatin immunoprecipitation followed by qPCR in the hippocampus revealed that two activating histone marks, H3K4Me3 and H3K27Ac, were enriched at specific endocannabinoid genes following cocaine intake. Targeting CB1 receptors using chromosome conformation capture, we highlighted spatial chromatin re-organization in the hippocampus, as well as in the nucleus accumbens, suggesting that destabilization of the chromatin may contribute to neuronal responses to cocaine. Overall, our results highlight a key role for the hippocampus in cocaine-induced plasticity and broaden the understanding of neuronal alterations associated with endocannabinoid signaling. The latter suggests that epigenetic modifications contribute to maladaptive behaviors associated with chronic drug use.
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