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Hypocretin/orexin knock‐out mice display disrupted behavioral and dopamine responses to cocaine
Author(s) -
Shaw Jessica K.,
Ferris Mark J.,
Locke Jason L.,
Brodnik Zachary D.,
Jones Sara R.,
España Rodrigo A.
Publication year - 2017
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.12432
Subject(s) - orexin , microdialysis , dopamine , conditioned place preference , neuroscience , nucleus accumbens , dopamine uptake inhibitors , in vivo , ventral tegmental area , locomotor activity , neuropeptide , psychology , chemistry , endocrinology , pharmacology , medicine , dopaminergic , biology , receptor , microbiology and biotechnology
The hypocretin/orexin (HCRT) system is implicated in reward and reinforcement processes through actions on the mesolimbic dopamine (DA) system. Here we provide evidence for the relationship between HCRT and DA in vivo in anesthetized and freely moving mice. The ability of cocaine to elicit reward‐related behaviors in mice lacking the HCRT prepro‐peptide (HCRT knock‐out; KO) and wild‐type controls was determined using conditioned place preference. Using a combination of microdialysis and in vivo fast scan cyclic voltammetry in anesthetized and freely moving mice, we investigated the underlying role of HCRT in the regulation of DA release and uptake. We show that, unlike wild‐type mice, HCRT KO mice fail to develop characteristic conditioned place preference for cocaine. These mice also demonstrated reduced DA release and uptake under baseline conditions in both anesthetized and freely moving experiments. Further, diminished DA signaling in HCRT KO mice persists following administration of cocaine. These findings indicate that HCRT is essential for the expression of behaviors associated with the rewarding effects of cocaine, and suggest that HCRT regulation of reward and reinforcement may be related to disruptions to DA neurotransmission.