CB1 Receptor Antagonism Blocks Stress-Potentiated Reinstatement of Cocaine Seeking in Rats

Authors

Jayme R. McReynolds, Marquette UniversityFollow
Elizabeth M. Doncheck, Marquette University
Oliver Vranjkovic, Marquette UniversityFollow
Geoffrey S. Ganzman, Marquette UniversityFollow
David A. Baker, Marquette UniversityFollow
Cecilia J. Hillard, Medical College of WisconsinFollow
John R. Mantsch, Marquette UniversityFollow

Document Type

Article

Language

eng

Format of Original

11 p.; 28 cm

Publication Date

1-2016

Publisher

Springer

Source Publication

Psychopharmacology

Source ISSN

0033-3158

Original Item ID

doi: 10.1007/s00213-015-4092-x; PubMed Central, PMCID: PMC4703460; Shelves: RM 315 .P75x 2016 v. 233, Memorial Periodicals

Abstract

Rationale

Under some conditions, stress, rather than directly triggering cocaine seeking, potentiates reinstatement to other stimuli, including a subthreshold cocaine dose. The mechanisms responsible for stress-potentiated reinstatement are not well defined. Endocannabinoid signaling is increased by stress and regulates synaptic transmission in brain regions implicated in motivated behavior.

Objectives

The objective of this study was to test the hypothesis that cannabinoid type 1 receptor (CB1R) signaling is required for stress-potentiated reinstatement of cocaine seeking in rats.

Methods

Following i.v. cocaine self-administration (2 h access/day) and extinction in male rats, footshock stress alone does not reinstate cocaine seeking but reinstatement is observed when footshock is followed by an injection of an otherwise subthreshold dose of cocaine (2.5 mg/kg, i.p.). CB1R involvement was tested by systemic administration of the CB1R antagonist AM251 (0, 1, or 3 mg/kg, i.p.) prior to testing for stress-potentiated reinstatement.

Results

Stress-potentiated reinstatement was blocked by both 1 and 3 mg/kg AM251. By contrast, AM251 only attenuated food-reinforced lever pressing at the higher dose (i.e., 3 mg/kg) and did not affect locomotor activity at either dose tested. Neither high-dose cocaine-primed reinstatement (10 mg/kg, i.p.) nor footshock stress-triggered reinstatement following long-access cocaine self-administration (6 h access/day) was affected by AM251 pretreatment. Footshock stress increased concentrations of both endocannabinoids, N-arachidonylethanolamine and 2-arachidonoylglycerol, in regions of the prefrontal cortex.

Conclusions

These findings demonstrate that footshock stress increases prefrontal cortical endocannabinoids and stress-potentiated reinstatement is CB1R-dependent, suggesting that CB1R is a potential therapeutic target for relapse prevention, particularly in individuals whose cocaine use is stress-related.

Comments

Accepted version. Psychopharmacology, Vol. 233, No. 1 (January 2016): 99-109. DOI. © 2015 Springer-Verlag Berlin Heidelberg. Used with permission.

Shareable Link. Provided by the Springer Nature SharedIt content-sharing initiative.

Recommended Citation

McReynolds, Jayme R.; Doncheck, Elizabeth M.; Vranjkovic, Oliver; Ganzman, Geoffrey S.; Baker, David A.; Hillard, Cecilia J.; and Mantsch, John R., "CB1 Receptor Antagonism Blocks Stress-Potentiated Reinstatement of Cocaine Seeking in Rats" (2016). Biomedical Sciences Faculty Research and Publications. 152.
https://epublications.marquette.edu/biomedsci_fac/152