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Neuropeptide Y system in accumbens shell mediates ethanol self‐administration in posterior ventral tegmental area
Author(s) -
Borkar Chandrashekhar D.,
Upadhya Manoj A.,
Shelkar Gajanan P.,
Subhedar Nishikant K.,
Kokare Dadasaheb M.
Publication year - 2016
Publication title -
addiction biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.445
H-Index - 78
eISSN - 1369-1600
pISSN - 1355-6215
DOI - 10.1111/adb.12254
Subject(s) - ventral tegmental area , nucleus accumbens , neuropeptide y receptor , stria terminalis , endocrinology , extended amygdala , medicine , self administration , dopamine , arc (geometry) , chemistry , dopaminergic , central nucleus of the amygdala , neuropeptide , amygdala , neuroscience , psychology , receptor , geometry , mathematics
Abstract Although modulatory effects of neuropeptide Y ( NPY ) on ethanol consumption are well established, its role in ethanol reward, in the framework of mesolimbic dopaminergic system, has not been studied. We investigated the influence of nucleus accumbens shell ( AcbS h) NPY ergic system on ethanol self‐administration in posterior ventral tegmental area (p‐ VTA ) using intracranial self‐administration paradigm. Rats were stereotaxically implanted with cannulae targeted unilaterally at the right p‐ VTA and trained to self‐administer ethanol (200 mg%) in standard two‐lever (active/inactive) operant chamber, an animal model with high predictive validity to test the rewarding mechanisms. Over a period of 7 days, these rats showed a significant increase in the number of lever presses for ethanol self‐administration suggesting reinforcement. While intra‐ AcbS h NPY (1 or 2 ng/rat) or [ L eu 31 , P ro 34 ]‐ NPY (0.5 or 1 ng/rat) dose‐dependently increased ethanol self‐administration, BIBP 3226 (0.4 or 0.8 ng/rat) produced opposite effect. The rats conditioned to self‐administer ethanol showed significant increase in the population of NPY ‐immunoreactive cells and fibres in the AcbSh, central nucleus of amygdala ( CeA ), hypothalamic arcuate nucleus ( ARC ) and lateral part of bed nucleus of stria terminalis as compared with that in the naïve rats. Neuronal tracing studies showed that NPY innervations in the AcbSh may derive from the neurons of ARC and CeA . As NPY and dopamine systems in reward areas are known to interact, we suggest that NPY inputs from ARC and CeA may play an important role in modulation of the dopaminergic system in the AcbS h and consequently influence the ethanol induced reward and addiction.