Open AccessKappa opioid receptor and dynorphin signaling in the central amygdala regulates alcohol intake
Author(s) -
Daniel W. Bloodgood,
J. Andrew Hardaway,
Christina M Stanhope,
Dipanwita Pati,
Melanie M. Pina,
Sofia Neira,
Shivani Desai,
Kristen M. Boyt,
Richard D. Palmiter,
Thomas L. Kash
Publication year - 2020
Publication title -
molecular psychiatry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.071
H-Index - 213
eISSN - 1476-5578
pISSN - 1359-4184
DOI - 10.1038/s41380-020-0690-z
Subject(s) - dynorphin , κ opioid receptor , knockout mouse , conditional gene knockout , amygdala , central nucleus of the amygdala , neuroscience , endogenous opioid , medicine , endocrinology , μ opioid receptor , receptor , opioid peptide , opioid , psychology , biology , gene , phenotype , genetics
Excessive alcohol drinking has been shown to modify brain circuitry to predispose individuals for future alcohol abuse. Previous studies have implicated the central nucleus of the amygdala (CeA) as an important site for mediating the somatic symptoms of withdrawal and for regulating alcohol intake. In addition, recent work has established a role for both the Kappa Opioid Receptor (KOR) and its endogenous ligand dynorphin in mediating these processes. However, it is unclear whether these effects are due to dynorphin or KOR arising from within the CeA itself or other input brain regions. To directly examine the role of preprodynorphin (PDYN) and KOR expression in CeA neurons, we performed region-specific conditional knockout of these genes and assessed the effects on the Drinking in the Dark (DID) and Intermittent Access (IA) paradigms. Conditional gene knockout resulted in sex-specific responses wherein PDYN knockout decreased alcohol drinking in both male and female mice, whereas KOR knockout decreased drinking in males only. We also found that neither PDYN nor KOR knockout protected against anxiety caused by alcohol drinking. Lastly, a history of alcohol drinking did not alter synaptic transmission in PDYN neurons in the CeA of either sex, but excitability of PDYN neurons was increased in male mice only. Taken together, our findings indicate that PDYN and KOR signaling in the CeA plays an important role in regulating excessive alcohol consumption and highlight the need for future studies to examine how this is mediated through downstream effector regions.