Impacts of chronic intermittent ethanol vapor and predator odor on ethanol intake and striatal D and CB cannabinoid receptor-expressing medium spiny neurons.

INTRODUCTION

Stress is a risk factor for ethanol use disorders, which has been modeled by chronic intermittent ethanol (CIE) vapor exposure. Repeated stress alters CB receptor signaling, which could influence ethanol-related behaviors. Striatal CB receptors regulate D-medium spiny neurons (D-MSNs), involved in goal-directed behaviors and stress responses. This study tested the hypothesis that predator odor stress interacts with CIE exposure to: (1) increase or accelerate CIE-induced escalation in ethanol intake, (2) increase plasma corticosterone levels, and (3) increase the expression or co-localization of CB receptors, D-MSNs, and Fos neuronal activation marker in the nucleus accumbens (NAc), dorsomedial (DMS), and dorsolateral (DLS) striatum.

METHODS

Male C57BL/6J mice underwent three cycles of 4 days CIE or air exposure, alternated with 5 days ethanol access. During the last two cycles, mice were exposed to predator odor or control bedding before each drinking session. Following the last stressor, brains were processed for RNAscope to label (encodes CB), (D), and (Fos).

RESULTS

As hypothesized, predator odor accelerated the CIE-induced increase in ethanol intake. Contrary to our expectations, CIE did not alter corticosterone levels after the final stressor. Compared to control bedding, predator odor reduced the percentage of + and triple-labeled + cells in NAc, but not dorsal striatum. In addition, CIE vs. Air exposure, increased percentages of +, double-labeled +, +, and triple + cells in the NAc, but not DMS or DLS.

DISCUSSION

Thus, CIE and stress elicited opposite neuroactivational effects on CB-regulated D-MSNs of the NAc. The role of these changes in stress- and CIE-augmented drinking warrants further investigation.