All Relations between reward and amygdala

Publication Sentence Publish Date Extraction Date Species
Angélica Torres-Berrio, Santiago Cuesta, Silvia Lopez-Guzman, Mauricio O Nava-Mes. Interaction Between Stress and Addiction: Contributions From Latin-American Neuroscience. Frontiers in psychology. vol 9. 2020-10-01. PMID:30622500. indeed, the hpa axis, the autonomic nervous system, and the extended amygdala, among other brain stress systems, interact with the brain's reward circuit involved in addictive behaviors. 2020-10-01 2023-08-13 human
Nicholas J Kelley, Alessia Gallucci, Paolo Riva, Leonor Josefina Romero Lauro, Brandon J Schmeiche. Stimulating Self-Regulation: A Review of Non-invasive Brain Stimulation Studies of Goal-Directed Behavior. Frontiers in behavioral neuroscience. vol 12. 2020-10-01. PMID:30713492. neuroscientific research has revealed that the prefrontal cortex plays a central role in self-regulation, specifically by exerting top-down control over subcortical regions involved in reward (e.g., striatum) and emotion (e.g., amygdala). 2020-10-01 2023-08-13 Not clear
Jasmin M Kizilirmak, Hannes Thuerich, Kristian Folta-Schoofs, Björn H Schott, Alan Richardson-Klaveh. Neural Correlates of Learning from Induced Insight: A Case for Reward-Based Episodic Encoding. Frontiers in psychology. vol 7. 2020-09-30. PMID:27847490. we found activation in the left striatum and parts of the left amygdala, pointing to a potential role of brain reward circuitry in the encoding of the solution words. 2020-09-30 2023-08-13 Not clear
Daniel T Gray, Lavanya Umapathy, Sara N Burke, Theodore P Trouard, Carol A Barne. Tract-Specific White Matter Correlates of Age-Related Reward Devaluation Deficits in Macaque Monkeys. Journal of neuroimaging in psychiatry & neurology. vol 3. issue 2. 2020-09-30. PMID:30198011. in macaques, ofc, but not amygdala volumes decline with age and correlate with performance on a reward devaluation (rd) task. 2020-09-30 2023-08-13 monkey
Valerie Lee Tryon, Sheri J Y Mizumor. A Novel Role for the Periaqueductal Gray in Consummatory Behavior. Frontiers in behavioral neuroscience. vol 12. 2020-09-30. PMID:30210313. anatomical work suggests the pag may mediate food intake and reward processing as it has extensive reciprocal connections within brain circuits that mediate appetitive processes and consummatory behaviors such as prefrontal cortex, hypothalamus, amygdala, parabrachial nucleus (pbn) and ventral tegmental area (kelley et al., 2005). 2020-09-30 2023-08-13 rat
Noriya Watanabe, Jamil P Bhanji, Hideki Ohira, Mauricio R Delgad. Reward-Driven Arousal Impacts Preparation to Perform a Task via Amygdala-Caudate Mechanisms. Cerebral cortex (New York, N.Y. : 1991). vol 29. issue 7. 2020-09-28. PMID:30060122. such failure trials were also associated with activation of the right amygdala representing pupil dilation, and the left caudate representing reward magnitude. 2020-09-28 2023-08-13 Not clear
Noriya Watanabe, Jamil P Bhanji, Hiroki C Tanabe, Mauricio R Delgad. Ventromedial prefrontal cortex contributes to performance success by controlling reward-driven arousal representation in amygdala. NeuroImage. vol 202. 2020-09-28. PMID:31470123. we recently examined neural representations of physiological arousal and potential reward magnitude during preparation, and found that performance failure was explained by relatively increased reward representation in the left caudate nucleus and arousal representation in the right amygdala (watanabe, et al., 2019). 2020-09-28 2023-08-13 Not clear
Madoka Anan, Ryoko Higa, Kenshiro Shikano, Masahito Shide, Akinobu Soda, Magdeline E Carrasco Apolinario, Kenji Mori, Toshitaka Shin, Mikiya Miyazato, Hiromitsu Mimata, Takatoshi Hikida, Toshikatsu Hanada, Kazuwa Nakao, Kenji Kangawa, Reiko Hanad. Cocaine has some effect on neuromedin U expressing neurons related to the brain reward system. Heliyon. vol 6. issue 5. 2020-09-28. PMID:32462086. in this study, we found that some of cocaine-induced c-fos immunoreactive cells were co-localized with nmu in the nucleus accumbens (nac), caudate putamen (cpu), and basolateral amygdala (bla), which are key brain regions associated with the brain reward system, in wild type mice. 2020-09-28 2023-08-13 mouse
Siyi Yu, Ana Ortiz, Randy L Gollub, Georgia Wilson, Jessica Gerber, Joel Park, Yiting Huang, Wei Shen, Suk-Tak Chan, Ajay D Wasan, Robert R Edwards, Vitaly Napadow, Ted J Kaptchuk, Bruce Rosen, Jian Kon. Acupuncture Treatment Modulates the Connectivity of Key Regions of the Descending Pain Modulation and Reward Systems in Patients with Chronic Low Back Pain. Journal of clinical medicine. vol 9. issue 6. 2020-09-28. PMID:32503194. our results suggest that acupuncture may simultaneously modulate the rsfc of key regions in the descending pain modulation (pag) and reward systems (vta), and the amygdala may be a key node linking the two systems to produce antinociceptive effects. 2020-09-28 2023-08-13 Not clear
Alice Servonnet, Giovanni Hernandez, Cynthia El Hage, Pierre-Paul Rompré, Anne-Noël Samah. Optogenetic Activation of the Basolateral Amygdala Promotes Both Appetitive Conditioning and the Instrumental Pursuit of Reward Cues. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 40. issue 8. 2020-08-17. PMID:31953370. optogenetic activation of the basolateral amygdala promotes both appetitive conditioning and the instrumental pursuit of reward cues. 2020-08-17 2023-08-13 rat
Shelley M Warlow, Erin E Naffziger, Kent C Berridg. The central amygdala recruits mesocorticolimbic circuitry for pursuit of reward or pain. Nature communications. vol 11. issue 1. 2020-08-17. PMID:32483118. the central amygdala recruits mesocorticolimbic circuitry for pursuit of reward or pain. 2020-08-17 2023-08-13 rat
Xiangyu Zhang, Joshua Kim, Susumu Tonegaw. Amygdala Reward Neurons Form and Store Fear Extinction Memory. Neuron. vol 105. issue 6. 2020-07-14. PMID:31952856. amygdala reward neurons form and store fear extinction memory. 2020-07-14 2023-08-13 Not clear
Xiangyu Zhang, Joshua Kim, Susumu Tonegaw. Amygdala Reward Neurons Form and Store Fear Extinction Memory. Neuron. vol 105. issue 6. 2020-07-14. PMID:31952856. here we demonstrate that a fear extinction memory engram is formed and stored in a genetically distinct basolateral amygdala (bla) neuronal population that drives reward behaviors and antagonizes the bla's original fear neurons. 2020-07-14 2023-08-13 Not clear
Jason A Avery, Alexander G Liu, John E Ingeholm, Cameron D Riddell, Stephen J Gotts, Alex Marti. Taste Quality Representation in the Human Brain. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 40. issue 5. 2020-07-09. PMID:31836661. however, our multivariate searchlight analyses were able to reliably decode the identity of distinct tastes within those mid-insula regions, as well as brain regions involved in affect and reward, such as the striatum, orbitofrontal cortex, and amygdala. 2020-07-09 2023-08-13 human
Olga Dal Monte, Cheng C J Chu, Nicholas A Fagan, Steve W C Chan. Specialized medial prefrontal-amygdala coordination in other-regarding decision preference. Nature neuroscience. vol 23. issue 4. 2020-07-07. PMID:32094970. here we investigated oscillatory neuronal interactions between the basolateral amygdala and the rostral anterior cingulate gyrus of the medial prefrontal cortex while monkeys expressed context-dependent positive or negative other-regarding preference (orp), whereby decisions affected the reward received by another monkey. 2020-07-07 2023-08-13 monkey
Rebecca L Tom, Aarit Ahuja, Hannah Maniates, Charlotte M Freeland, Mike J F Robinso. Optogenetic activation of the central amygdala generates addiction-like preference for reward. The European journal of neuroscience. vol 50. issue 3. 2020-06-30. PMID:29797474. optogenetic activation of the central amygdala generates addiction-like preference for reward. 2020-06-30 2023-08-13 rat
Dominik R Bach, Martina Hoffmann, Carsten Finke, Rene Hurlemann, Christoph J Plone. Disentangling Hippocampal and Amygdala Contribution to Human Anxiety-Like Behavior. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 39. issue 43. 2020-06-30. PMID:31501296. we conclude that deciding to approach reward under threat relies on hippocampus but not amygdala, whereas vigor of returning to safety depends on amygdala but not on hippocampus. 2020-06-30 2023-08-13 human
Bernd Krämer, Esther K Diekhof, Oliver Grube. Effects of city living on the mesolimbic reward system-An fmri study. Human brain mapping. vol 38. issue 7. 2020-06-15. PMID:28397390. besides its influence on the amygdala, chronic stress also affects mesocorticolimbic brain regions involved in reward processing, and stress-related dysregulation of the mesocorticolimbic dopamine system is thought to contribute to onset and manifestation of psychiatric disorders. 2020-06-15 2023-08-13 human
Bernd Krämer, Esther K Diekhof, Oliver Grube. Effects of city living on the mesolimbic reward system-An fmri study. Human brain mapping. vol 38. issue 7. 2020-06-15. PMID:28397390. city dwellers also revealed increased responses in other brain regions involved in reward processing and in the regulation of stress and emotions, such as amygdala, orbitofrontal, and pregenual anterior cingulate cortex. 2020-06-15 2023-08-13 human
Lindsay C Hanford, Kristen Eckstrand, Anna Manelis, Danella M Hafeman, John Merranko, Cecile D Ladouceur, Simona Graur, Alicia McCaffrey, Kelly Monk, Lisa K Bonar, Mary Beth Hickey, Tina R Goldstein, Benjamin I Goldstein, David Axelson, Genna Bebko, Michele A Bertocci, Mary Kay Gill, Boris Birmaher, Mary L Phillip. The impact of familial risk and early life adversity on emotion and reward processing networks in youth at-risk for bipolar disorder. PloS one. vol 14. issue 12. 2020-03-26. PMID:31830059. interaction effects were found between risk calculator scores, negative sles score and activity in right amygdala and bilateral fusiform gyri during the emotion processing task, as well as activity in the fronto-, striatal, and parietal regions during the reward processing task. 2020-03-26 2023-08-13 Not clear