The selective κ-opioid receptor antagonist JDTic attenuates the alcohol deprivation effect in rats

• Published in: European neuropsychopharmacology Vol. 29; no. 12; pp. 1386 - 1396
• Main Authors: Uhari-Väänänen, Johanna, Eteläinen, Tony, Bäckström, Pia, Oinio, Ville, Carroll, F. Ivy, Raasmaja, Atso, Kiianmaa, Kalervo, Piepponen, Petteri
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01.12.2019
• Subjects: Ethanol; Kappa opioid receptor; Nucleus accumbens; Relapse; Nucleus accumbens; Relapse; Ethanol; Kappa opioid receptor
• ISSN: 0924-977X; 1873-7862
• DOI: 10.1016/j.euroneuro.2019.10.003

•Systemic and intra-accumbens shell JDTic, a κ-antagonist, attenuated the ADE in rats.•A low dose of naltrexone inhibited the ADE and decreased ethanol intake.•κ-Opioidergic mechanisms may participate in mediating relapse to ethanol intake. The mechanisms behind relapse to ethanol intake in recovering alcoholics are still unclear. The negative reinforcing effects contributing to ethanol addiction, including relapse, are considered to be partly driven by the κ-opioidergic system. As the κ-opioidergic system interacts with the mesolimbic reward pathway, the aim of the study was to clarify the role of nucleus accumbens shell κ-opioidergic mechanisms in relapse to ethanol intake by using the alcohol deprivation effect (ADE) paradigm. The ADE is defined as a transient increase in voluntary ethanol intake after a forced period of abstinence. Male Long-Evans rats were trained to voluntarily consume 10% (v/v) ethanol solution. Ethanol access and deprivation cycles were initiated after stable ethanol intake baselines had been reached and bilateral guide cannulas had been implanted above the nucleus accumbens shell. One cycle consisted of 10 days of 90 min access to ethanol followed by 6 days of ethanol deprivation. The ADE was measured in the beginning of a new cycle. Rats received JDTic, a selective κ-antagonist, either subcutaneously (10 mg/kg) or intra-accumbally (15 µg/site) or, as a reference substance, systemic naltrexone (0.3 mg/kg) before ethanol re-access, and the effects on the ADE were evaluated. Systemic and intra-accumbal JDTic significantly attenuated the ADE on the first day of ethanol re-access, as did systemic naltrexone. Additionally, naltrexone decreased ethanol intake levels. These results suggest that nucleus accumbens shell κ-opioidergic mechanisms may have a role in mediating relapse to ethanol intake. Additionally, κ-antagonism could be a valuable adjunct in ethanol relapse prevention.