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A GABAergic Projection from the Centromedial Nuclei of the Amygdala to Ventromedial Prefrontal Cortex Modulates Reward Behavior.
Seo, Dong-Oh; Funderburk, Samuel C; Bhatti, Dionnet L; Motard, Laura E; Newbold, Dillan; Girven, Kasey S; McCall, Jordan G; Krashes, Michael; Sparta, Dennis R; Bruchas, Michael R.
Afiliación
  • Seo DO; Department of Anesthesiology, Division of Basic Research.
  • Funderburk SC; Department of Anesthesiology, Division of Basic Research.
  • Bhatti DL; Diabetes, Endocrinology and Obesity Branch, National Institutes of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892, and.
  • Motard LE; Department of Anesthesiology, Division of Basic Research.
  • Newbold D; Department of Anesthesiology, Division of Basic Research.
  • Girven KS; Department of Anesthesiology, Division of Basic Research.
  • McCall JG; Department of Anatomy and Neurobiology, University of Maryland School of Medicine, Baltimore, Maryland 21201.
  • Krashes M; Department of Anesthesiology, Division of Basic Research.
  • Sparta DR; Diabetes, Endocrinology and Obesity Branch, National Institutes of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892, and.
  • Bruchas MR; Department of Anatomy and Neurobiology, University of Maryland School of Medicine, Baltimore, Maryland 21201.
J Neurosci ; 36(42): 10831-10842, 2016 10 19.
Article en En | MEDLINE | ID: mdl-27798138
The neural circuitry underlying mammalian reward behaviors involves several distinct nuclei throughout the brain. It is widely accepted that the midbrain dopamine (DA) neurons are critical for the reward-related behaviors. Recent studies have shown that the centromedial nucleus of the amygdala (CeMA) has a distinct role in regulating reward-related behaviors. However, the CeMA and ventromedial PFC (vmPFC) interaction in reward regulation remains poorly understood. Here, we identify and dissect a GABAergic projection that originates in the CeMA and terminates in the vmPFC (VGat-CreCeMA-vmPFC) using viral-vector-mediated, cell-type-specific optogenetic techniques in mice. Pathway-specific optogenetic activation of the VGat-CreCeMA-vmPFC circuit in awake, behaving animals produced a positive, reward-like phenotype in real-time place preference and increased locomotor activity in open-field testing. In sucrose operant conditioning, the photoactivation of these terminals increased nose-poking effort with no effect on licking behavior and robustly facilitated the extinction of operant behavior. However, photoactivation of these terminals did not induce self-stimulation in the absence of an external reward. The results described here suggest that the VGat-CreCeMA-vmPFC projection acts to modulate existing reward-related behaviors. SIGNIFICANCE STATEMENT: Many studies have shown that the interactions between the centromedial nucleus of the amygdala (CeMA) and ventromedial PFC (vmPFC) have critical roles for emotional regulation. However, most studies have associated this circuit with fear and anxiety behaviors and emphasized top-down processing from vmPFC to CeMA. Here, we provide new evidence for bottom-up CeMA to vmPFC influence on reward-related behaviors. Although previous work implicated the CeMA in incentive salience, our results isolate the investigation to a specific CeMA GABAergic projection to the vmPFC. This long-range GABAergic interaction between amygdala and frontal cortex adds a new dimension to the complex regulation of reward-related behaviors.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Recompensa / Conducta Animal / Corteza Prefrontal / Ácido gamma-Aminobutírico / Amígdala del Cerebelo Límite: Animals Idioma: En Revista: J Neurosci Año: 2016 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Recompensa / Conducta Animal / Corteza Prefrontal / Ácido gamma-Aminobutírico / Amígdala del Cerebelo Límite: Animals Idioma: En Revista: J Neurosci Año: 2016 Tipo del documento: Article
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