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Erik B. Oleson

Researcher at University of Colorado Denver

Publications -  48
Citations -  2390

Erik B. Oleson is an academic researcher from University of Colorado Denver. The author has contributed to research in topics: Dopamine & Nucleus accumbens. The author has an hindex of 22, co-authored 47 publications receiving 2087 citations. Previous affiliations of Erik B. Oleson include University of Colorado Boulder & Wake Forest University.

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The hypocretin–orexin system regulates cocaine self‐administration via actions on the mesolimbic dopamine system

TL;DR: These studies suggest that hypocretin neurotransmission participates in reinforcement processes, likely through modulation of the mesolimbic dopamine system, and suggest that the hypoc retin system may provide a target for pharmacotherapies to treat cocaine addiction.
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Subsecond Dopamine Release in the Nucleus Accumbens Predicts Conditioned Punishment and Its Successful Avoidance

TL;DR: Data show that subsecond fluctuations in mesolimbic dopamine release predict when rats will successfully avoid punishment and differentially encode cues related to aversive outcomes.
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Behavioral and neurochemical phenotyping of Homer1 mutant mice: Possible relevance to schizophrenia

TL;DR: Behavioral and neurochemical data derived from Homer1 mutant mice are consistent with the recent association of schizophrenia with a single‐nucleotide polymorphism in the Homer1 gene and suggest that the regulation of extracellular levels of glutamate within limbo‐corticostriatal structures by Homer 1 gene products may be involved in the pathogenesis of this neuropsychiatric disorder.
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Homer2 is necessary for EtOH-induced neuroplasticity.

TL;DR: Constitutive Homer2 gene deletion and rescue with adeno-associated viral transfection of Homer2b was used to demonstrate the importance of Homer proteins in neuroplasticity produced by repeated ethanol (EtOH) administration and a necessary and active role for accumbens Homer2 expression in regulating EtOH-induced behavioral and cellular neuroplasticsity.
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Endocannabinoids shape accumbal encoding of cue-motivated behavior via CB1 receptor activation in the ventral tegmentum

TL;DR: It is suggested that 2AG in the VTA regulates reward seeking by sculpting ethologically relevant patterns of dopamine release during reward-directed behavior by augmenting levels of the endocannabinoid 2-arachidonoylglycerol (2AG).