| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Julien Vitay, Fred H Hamke. Timing and expectation of reward: a neuro-computational model of the afferents to the ventral tegmental area. Frontiers in neurorobotics. vol 8. 2014-02-19. PMID:24550821. |
while associative learning occurs primarily in the amygdala, learning of the temporal relationship between the cue and the associated reward is implemented as a dopamine-modulated coincidence detection mechanism in the nucleus accumbens. |
2014-02-19 |
2023-08-12 |
Not clear |
| Gregor Kohls, Martin Schulte-Rüther, Barbara Nehrkorn, Kristin Müller, Gereon R Fink, Inge Kamp-Becker, Beate Herpertz-Dahlmann, Robert T Schultz, Kerstin Konra. Reward system dysfunction in autism spectrum disorders. Social cognitive and affective neuroscience. vol 8. issue 5. 2014-01-29. PMID:22419119. |
in particular, diminished activation in the nucleus accumbens was observed when money, but not when social reward, was at stake, whereas the amygdala and anterior cingulate cortex were hypoactivated within the asd group in response to both rewards. |
2014-01-29 |
2023-08-12 |
human |
| Pascal Vrticka, Jessica M Black, Allan L Reis. The neural basis of humour processing. Nature reviews. Neuroscience. vol 14. issue 12. 2014-01-13. PMID:24169937. |
humour seems to engage a core network of cortical and subcortical structures, including temporo-occipito-parietal areas involved in detecting and resolving incongruity (mismatch between expected and presented stimuli); and the mesocorticolimbic dopaminergic system and the amygdala, key structures for reward and salience processing. |
2014-01-13 |
2023-08-12 |
human |
| Satoshi Terada, Susumu Takahashi, Yoshio Sakura. Oscillatory interaction between amygdala and hippocampus coordinates behavioral modulation based on reward expectation. Frontiers in behavioral neuroscience. vol 7. 2013-12-18. PMID:24348352. |
we simultaneously recorded neuronal spikes and local field potential from the basolateral amygdala and hippocampal ca1 while rats were performing a light-side discrimination task with different expectations of a high or low probability of reward delivery. |
2013-12-18 |
2023-08-12 |
rat |
| Satoshi Terada, Susumu Takahashi, Yoshio Sakura. Oscillatory interaction between amygdala and hippocampus coordinates behavioral modulation based on reward expectation. Frontiers in behavioral neuroscience. vol 7. 2013-12-18. PMID:24348352. |
we propose that the amygdala influences firing rates and the strength of synchronization of hippocampal neurons through coherent oscillation, which is a part of the mechanism of how reward expectations modulate goal-directed behavior. |
2013-12-18 |
2023-08-12 |
rat |
| Glenn R Fox, Mona Sobhani, Lisa Aziz-Zade. Witnessing hateful people in pain modulates brain activity in regions associated with physical pain and reward. Frontiers in psychology. vol 4. 2013-10-29. PMID:24167496. |
functional connectivity analyses revealed connections between seed regions in the left acc and right insular cortex with reward regions, the amygdala, and frontal regions associated with emotion regulation. |
2013-10-29 |
2023-08-12 |
human |
| Danielle M Judice-Daher, José Lino O Buen. Lesions of the nucleus accumbens disrupt reinforcement omission effects in rats. Behavioural brain research. vol 252. 2013-10-28. PMID:23796973. |
recent neuroimaging studies in human revealed reward delivery enhances activity of subcortical structures (nac and amygdala), whereas reward omission reduces the activity in these same structures. |
2013-10-28 |
2023-08-12 |
human |
| Bihua Bie, Yan Wang, You-Qing Cai, Zhi Zhang, Yuan-Yuan Hou, Zhizhong Z Pa. Upregulation of nerve growth factor in central amygdala increases sensitivity to opioid reward. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology. vol 37. issue 13. 2013-08-26. PMID:22871918. |
upregulation of nerve growth factor in central amygdala increases sensitivity to opioid reward. |
2013-08-26 |
2023-08-12 |
rat |
| R Shao, J Read, T E J Behrens, R D Roger. Shifts in reinforcement signalling while playing slot-machines as a function of prior experience and impulsivity. Translational psychiatry. vol 3. 2013-08-13. PMID:23443361. |
impulsivity, itself linked to problem gambling and heightened vulnerability to other addictive disorders, is associated with divergent coding of winning outcomes and almost-winning experiences within the ventral striatum and amygdala, potentially enhancing the reward value of successful slot-machine game outcomes but, at the same time,modulating the aversive motivational consequences of near-miss outcomes. |
2013-08-13 |
2023-08-12 |
human |
| Dean Mobbs, Demis Hassabis, Rongjun Yu, Carlton Chu, Matthew Rushworth, Erie Boorman, Tim Dalgleis. Foraging under competition: the neural basis of input-matching in humans. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 33. issue 23. 2013-08-06. PMID:23739983. |
moreover, amygdala and dorsal putamen activity steered interindividual preferences in competition avoidance and pursuing reward. |
2013-08-06 |
2023-08-12 |
human |
| George F Koo. Addiction is a Reward Deficit and Stress Surfeit Disorder. Frontiers in psychiatry. vol 4. 2013-08-05. PMID:23914176. |
specific neurochemical elements in these structures include not only decreases in reward system function (within-system opponent processes) but also recruitment of the brain stress systems mediated by corticotropin-releasing factor (crf) and dynorphin-κ opioid systems in the ventral striatum, extended amygdala, and frontal cortex (both between-system opponent processes). |
2013-08-05 |
2023-08-12 |
Not clear |
| K P Maruska, A Zhang, A Neboori, R D Fernal. Social opportunity causes rapid transcriptional changes in the social behaviour network of the brain in an African cichlid fish. Journal of neuroendocrinology. vol 25. issue 2. 2013-07-12. PMID:22958303. |
several receptor mrna changes occurred in regions with putative homologies to the mammalian septum and extended amygdala, two regions shared by sbn and reward circuits, suggesting an important role in the integration of social salience, stressors, hormonal state and adaptive behaviours. |
2013-07-12 |
2023-08-12 |
Not clear |
| Shambhu Bhat, David T Dao, Chantelle E Terrillion, Michal Arad, Robert J Smith, Nikolai M Soldatov, Todd D Goul. CACNA1C (Cav1.2) in the pathophysiology of psychiatric disease. Progress in neurobiology. vol 99. issue 1. 2013-07-10. PMID:22705413. |
ca(v)1.2 is involved in the proper function of numerous neurological circuits including those involving the hippocampus, amygdala, and mesolimbic reward system, which are strongly implicated in psychiatric disease pathophysiology. |
2013-07-10 |
2023-08-12 |
human |
| R Shao, J Read, T E J Behrens, R D Roger. Shifts in reinforcement signalling while playing slot-machines as a function of prior experience and impulsivity. Translational psychiatry. vol 3. 2013-07-04. PMID:23321810. |
impulsivity, itself linked to problem gambling and heightened vulnerability to other addictive disorders, is associated with divergent coding of winning outcomes and almost-winning experiences within the ventral striatum and amygdala, potentially enhancing the reward value of successful slot-machine game outcomes but, at the same time, modulating the aversive motivational consequences of near-miss outcomes. |
2013-07-04 |
2023-08-12 |
human |
| I A Mendez, J C Damborsky, U H Winzer-Serhan, J L Bizon, B Setlo. Α4β2 and α7 nicotinic acetylcholine receptor binding predicts choice preference in two cost benefit decision-making tasks. Neuroscience. vol 230. 2013-07-01. PMID:23159316. |
similar trends suggested that choice of the large delayed reward in the delay discounting task was inversely related to α4β2 receptor binding in the orbitofrontal cortex, nucleus accumbens core, and basolateral amygdala, as well as to α7 receptor binding in the basolateral amygdala. |
2013-07-01 |
2023-08-12 |
rat |
| Carolyn H Declerck, Christophe Boone, Griet Emond. When do people cooperate? The neuroeconomics of prosocial decision making. Brain and cognition. vol 81. issue 1. 2013-06-19. PMID:23174433. |
specifically, we propose that the motivation to cooperate (or not), generated by the reward system in the brain (extending from the striatum to the ventromedial prefrontal cortex), is modulated by two neural networks: a cognitive control system (centered on the lateral prefrontal cortex) that processes extrinsic cooperative incentives, and/or a social cognition system (including the temporo-parietal junction, the medial prefrontal cortex and the amygdala) that processes trust and/or threat signals. |
2013-06-19 |
2023-08-12 |
Not clear |
| Jing Liu, Ying Hao, Minyi Du, Xiaoying Wang, Jue Zhang, Brad Manor, Xuexiang Jiang, Wenxue Fang, Dongxin Wan. Quantitative cerebral blood flow mapping and functional connectivity of postherpetic neuralgia pain: a perfusion fMRI study. Pain. vol 154. issue 1. 2013-06-18. PMID:23140909. |
functional connectivity results demonstrated that the reward circuitry involved in striatum, prefrontal cortex, amygdala, and parahippocampal gyrus and the circuitry among striatum, thalamus, and insula were highly correlated with each element in phn patients. |
2013-06-18 |
2023-08-12 |
human |
| Min J Kang, Colin F Camere. fMRI evidence of a hot-cold empathy gap in hypothetical and real aversive choices. Frontiers in neuroscience. vol 7. 2013-06-18. PMID:23772205. |
fmri shows that real choice more strongly activates striatum and medial prefrontal cortex (reward regions) and shows distinct activity in insula and amygdala (disgust and fear regions). |
2013-06-18 |
2023-08-12 |
Not clear |
| M Waraczynski, W Zwifelhofer, L Kueh. Brain stimulation reward is altered by affecting dopamine-glutamate interactions in the central extended amygdala. Neuroscience. vol 224. 2013-06-17. PMID:22906479. |
brain stimulation reward is altered by affecting dopamine-glutamate interactions in the central extended amygdala. |
2013-06-17 |
2023-08-12 |
rat |
| M Waraczynski, W Zwifelhofer, L Kueh. Brain stimulation reward is altered by affecting dopamine-glutamate interactions in the central extended amygdala. Neuroscience. vol 224. 2013-06-17. PMID:22906479. |
this work compares the effects on brain stimulation reward (bsr) when combining d2 dopamine receptor and ampa glutamate receptor manipulations in the sublenticular central extended amygdala (sleac) and the nucleus accumbens shell (nac shell). |
2013-06-17 |
2023-08-12 |
rat |