| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| David J Rademacher, Beatrix Kovacs, Fei Shen, T Celeste Napier, Gloria E Meredit. The neural substrates of amphetamine conditioned place preference: implications for the formation of conditioned stimulus-reward associations. The European journal of neuroscience. vol 24. issue 7. 2006-12-21. PMID:17067306. |
the formation of conditioned stimulus-amphetamine reward associations is accompanied by tyrosine kinase b receptor expression in the basolateral amygdala and dentate gyrus, ca1 and ca3 fields of the hippocampus. |
2006-12-21 |
2023-08-12 |
human |
| E C Hinton, A J Holland, M S N Gellatly, S Soni, A M Owe. An investigation into food preferences and the neural basis of food-related incentive motivation in Prader-Willi syndrome. Journal of intellectual disability research : JIDR. vol 50. issue Pt 9. 2006-12-05. PMID:16901290. |
the aim of this study was to examine the role of the reward system in such eating behaviour, in terms of both the pattern of food preferences and the neural substrates of incentive in the amygdala and orbitofrontal cortex (ofc). |
2006-12-05 |
2023-08-12 |
Not clear |
| Michelle A Riley, Ilona Vath. Mid- to late gestational morphine exposure does not alter the rewarding properties of morphine in adult male rats. Neuropharmacology. vol 51. issue 2. 2006-12-04. PMID:16697425. |
both the nucleus accumbens and central amygdala play important roles in modulating drug-induced reward via the mesolimbic dopaminergic system. |
2006-12-04 |
2023-08-12 |
rat |
| Feng C Zhou, Robert N Sahr, Youssef Sari, Kamran Behbahan. Glutamate and dopamine synaptic terminals in extended amygdala after 14-week chronic alcohol drinking in inbred alcohol-preferring rats. Alcohol (Fayetteville, N.Y.). vol 39. issue 1. 2006-10-06. PMID:16938628. |
alcohol has been shown to affect glutamate (glu) and dopamine (da) release and their correlated receptors in the key reward center--extended amygdala--which includes the shell of nucleus accumbens (snac) and central nucleus of amygdala (camg). |
2006-10-06 |
2023-08-12 |
rat |
| Lino Becerra, Kim Harter, R Gilberto Gonzalez, David Borsoo. Functional magnetic resonance imaging measures of the effects of morphine on central nervous system circuitry in opioid-naive healthy volunteers. Anesthesia and analgesia. vol 103. issue 1. 2006-08-16. PMID:16790655. |
infusion of morphine, but not saline, elicited mild euphoria without aversive symptoms and resulted in positive signal changes in reward structures including the nucleus accumbens, sublenticular extended amygdala, orbitofrontal cortex, and hippocampus. |
2006-08-16 |
2023-08-12 |
human |
| Meg A Waraczynsk. The central extended amygdala network as a proposed circuit underlying reward valuation. Neuroscience and biobehavioral reviews. vol 30. issue 4. 2006-08-11. PMID:16243397. |
the central extended amygdala network as a proposed circuit underlying reward valuation. |
2006-08-11 |
2023-08-12 |
Not clear |
| Meg A Waraczynsk. The central extended amygdala network as a proposed circuit underlying reward valuation. Neuroscience and biobehavioral reviews. vol 30. issue 4. 2006-08-11. PMID:16243397. |
the proposed network circuitry underlying self-stimulation is also placed into the larger context of basal forebrain function, specifically, the role of the ventral striatopallidum in linking motivation to behavior, the role of the amygdala in detecting motivationally significant inputs, and the role of the magnocellular complex in communicating reward information to cortical and hippocampal targets. |
2006-08-11 |
2023-08-12 |
Not clear |
| Michael J Glass, Paul J Kruzich, Eric E O Colago, Mary Jeanne Kreek, Virginia M Picke. Increased AMPA GluR1 receptor subunit labeling on the plasma membrane of dendrites in the basolateral amygdala of rats self-administering morphine. Synapse (New York, N.Y.). vol 58. issue 1. 2006-06-28. PMID:16037950. |
these drug-dependent neural adaptations may occur within brain systems that mediate reward, emotion, and cognitive function such as the amygdala complex. |
2006-06-28 |
2023-08-12 |
rat |
| John D Beaver, Andrew D Lawrence, Jenneke van Ditzhuijzen, Matt H Davis, Andrew Woods, Andrew J Calde. Individual differences in reward drive predict neural responses to images of food. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 26. issue 19. 2006-05-31. PMID:16687507. |
a network of interconnected brain regions, including orbitofrontal, ventral striatal, amygdala, and midbrain areas, has been widely implicated in a number of aspects of food reward. |
2006-05-31 |
2023-08-12 |
human |
| E J Van Bockstaele, C Rudoy, P Mannelli, V Oropeza, Y Qia. Elevated mu-opioid receptor expression in the nucleus of the solitary tract accompanies attenuated withdrawal signs after chronic low dose naltrexone in opiate-dependent rats. Journal of neuroscience research. vol 83. issue 3. 2006-05-25. PMID:16385558. |
in this study, to determine whether similar cellular changes occurred in forebrain nuclei associated with drug reward, expressions of pka and pcreb were analyzed in the ventral tegmental area, frontal cortex, striatum, and amygdala of opiate-treated rats that received low doses of naltrexone in their drinking water. |
2006-05-25 |
2023-08-12 |
rat |
| D S Kosson, S Budhani, M Nakic, G Chen, Z S Saad, M Vythilingam, D S Pine, R J R Blai. The role of the amygdala and rostral anterior cingulate in encoding expected outcomes during learning. NeuroImage. vol 29. issue 4. 2006-05-17. PMID:16387514. |
the amygdala and reward. |
2006-05-17 |
2023-08-12 |
human |
| Alexander W Johnson, David M Bannerman, Nicholas P Rawlins, Rolf Sprengel, Mark A Goo. Impaired outcome-specific devaluation of instrumental responding in mice with a targeted deletion of the AMPA receptor glutamate receptor 1 subunit. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 25. issue 9. 2006-03-31. PMID:15745962. |
these deficits mirror those seen after lesions of the basolateral amygdala and suggests that glur1-mediated neurotransmission in this region contributes to encoding the relationship between sensory-specific aspects of reward and their incentive value. |
2006-03-31 |
2023-08-12 |
mouse |
| Laurie L Wellman, Karen Gale, Ludise Malkov. GABAA-mediated inhibition of basolateral amygdala blocks reward devaluation in macaques. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 25. issue 18. 2006-03-23. PMID:15872105. |
gabaa-mediated inhibition of basolateral amygdala blocks reward devaluation in macaques. |
2006-03-23 |
2023-08-12 |
monkey |
| Laurie L Wellman, Karen Gale, Ludise Malkov. GABAA-mediated inhibition of basolateral amygdala blocks reward devaluation in macaques. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 25. issue 18. 2006-03-23. PMID:15872105. |
here, we tested the hypothesis that transient inactivation of amygdala by the gaba(a) agonist muscimol (mus), specifically during the period of reward satiation, would have a similar effect. |
2006-03-23 |
2023-08-12 |
monkey |
| Sylvia M L Cox, Alexandre Andrade, Ingrid S Johnsrud. Learning to like: a role for human orbitofrontal cortex in conditioned reward. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 25. issue 10. 2006-03-02. PMID:15758183. |
recent functional neuroimaging studies have implicated the ventral striatum, orbitofrontal cortex (ofc), and amygdala in the representation of reward values and/or in the anticipation of rewarding events. |
2006-03-02 |
2023-08-12 |
human |
| Henrik Walter, Birgit Abler, Angela Ciaramidaro, Susanne Er. Motivating forces of human actions. Neuroimaging reward and social interaction. Brain research bulletin. vol 67. issue 5. 2006-02-28. PMID:16216683. |
for reward it has been shown that a system exists in humans that is involved in predicting rewards and thus guides behaviour, involving a circuit including the striatum, the orbitofrontal cortex and the amygdala. |
2006-02-28 |
2023-08-12 |
human |
| Yasuko Sugase-Miyamoto, Barry J Richmon. Neuronal signals in the monkey basolateral amygdala during reward schedules. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 25. issue 48. 2006-02-27. PMID:16319307. |
neuronal signals in the monkey basolateral amygdala during reward schedules. |
2006-02-27 |
2023-08-12 |
monkey |
| Yasuko Sugase-Miyamoto, Barry J Richmon. Neuronal signals in the monkey basolateral amygdala during reward schedules. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 25. issue 48. 2006-02-27. PMID:16319307. |
we suggest that basolateral amygdala, by anticipating and then delineating the schedule and representing reward contingency, provide contextual information that is important for adjusting motivational level as a function of immediate behavior goals. |
2006-02-27 |
2023-08-12 |
monkey |
| Edmund T Rolls, Jian-Zhong Xian. Reward-spatial view representations and learning in the primate hippocampus. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 25. issue 26. 2006-02-14. PMID:15987946. |
the primate anterior hippocampus (which corresponds to the rodent ventral hippocampus) receives inputs from brain regions involved in reward processing, such as the amygdala and orbitofrontal cortex. |
2006-02-14 |
2023-08-12 |
Not clear |
| Richard A Depue, Jeannine V Morrone-Strupinsk. A neurobehavioral model of affiliative bonding: implications for conceptualizing a human trait of affiliation. The Behavioral and brain sciences. vol 28. issue 3. 2006-01-20. PMID:16209725. |
affiliative stimuli, in particular, are incorporated within contextual ensembles predictive of affiliative reward via: (a) the binding of affiliative stimuli in the rostral circuit of the medial extended amygdala and subsequent transmission to the nas shell; (b) affiliative stimulus-induced opiate potentiation of da processes in the vta and nas; and (c) permissive or facilitatory effects of gonadal steroids, oxytocin (in interaction with da), and vasopressin on (i) sensory, perceptual, and attentional processing of affiliative stimuli and (ii) formation of social memories. |
2006-01-20 |
2023-08-12 |
human |