All Relations between reward and amygdala

Publication Sentence Publish Date Extraction Date Species
Martin Kavaliers, Klaus-Peter Ossenkopp, Cashmeira-Dove Tyson, Indra R Bishnoi, Elena Choleri. Social factors and the neurobiology of pathogen avoidance. Biology letters. vol 18. issue 2. 2022-02-23. PMID:35193366. social vigilance, social distancing (approach/avoidance), social salience and social reward); (iii) the roles of various brain regions (in particular the amygdala and insular cortex) and neuromodulators (neurotransmitters, neuropeptides, steroidal hormones and immune components) in the regulation of pathogen avoidance. 2022-02-23 2023-08-13 Not clear
Viktor S Kokhan, Petr K Anokhin, Denis A Abaimov, Inna Yu Shamakina, Vladislav O Soldatov, Alexey V Deyki. Neurokinin-1 receptor antagonist rolapitant suppresses anxiety and alcohol intake produced by repeated withdrawal episodes. The FEBS journal. 2022-02-17. PMID:35175687. administration, rolapitant rapidly penetrated into specific rat brain regions - amygdala, hypothalamus and neocortex - implicated in the control of anxiety and reward. 2022-02-17 2023-08-13 rat
Luis Manssuer, Ding Qiong, Liu Wei, Ruoqi Yang, Chencheng Zhang, Yijie Zhao, Bomin Sun, Shikun Zhan, Valerie Voo. Integrated Amygdala, Orbitofrontal and Hippocampal Contributions to Reward and Loss Coding Revealed with Human Intracranial EEG. The Journal of neuroscience : the official journal of the Society for Neuroscience. 2022-02-12. PMID:35149513. integrated amygdala, orbitofrontal and hippocampal contributions to reward and loss coding revealed with human intracranial eeg. 2022-02-12 2023-08-13 human
Luis Manssuer, Ding Qiong, Liu Wei, Ruoqi Yang, Chencheng Zhang, Yijie Zhao, Bomin Sun, Shikun Zhan, Valerie Voo. Integrated Amygdala, Orbitofrontal and Hippocampal Contributions to Reward and Loss Coding Revealed with Human Intracranial EEG. The Journal of neuroscience : the official journal of the Society for Neuroscience. 2022-02-12. PMID:35149513. neurophysiological work in primates and rodents have shown the amygdala plays a central role in reward processing through connectivity with the orbitofrontal cortex (ofc) and hippocampus. 2022-02-12 2023-08-13 human
Luis Manssuer, Ding Qiong, Liu Wei, Ruoqi Yang, Chencheng Zhang, Yijie Zhao, Bomin Sun, Shikun Zhan, Valerie Voo. Integrated Amygdala, Orbitofrontal and Hippocampal Contributions to Reward and Loss Coding Revealed with Human Intracranial EEG. The Journal of neuroscience : the official journal of the Society for Neuroscience. 2022-02-12. PMID:35149513. anticipation of reward increased high frequency gamma (hfg) (60-250 hz) activity in the hippocampus and theta band (4-8 hz) synchronization between amygdala and ofc, suggesting roles in memory and motivation. 2022-02-12 2023-08-13 human
Luis Manssuer, Ding Qiong, Liu Wei, Ruoqi Yang, Chencheng Zhang, Yijie Zhao, Bomin Sun, Shikun Zhan, Valerie Voo. Integrated Amygdala, Orbitofrontal and Hippocampal Contributions to Reward and Loss Coding Revealed with Human Intracranial EEG. The Journal of neuroscience : the official journal of the Society for Neuroscience. 2022-02-12. PMID:35149513. during receipt, hfg in the amygdala was involved in outcome value coding, the ofc cue context-specific outcome value comparison and the hippocampus reward coding. 2022-02-12 2023-08-13 human
Luis Manssuer, Ding Qiong, Liu Wei, Ruoqi Yang, Chencheng Zhang, Yijie Zhao, Bomin Sun, Shikun Zhan, Valerie Voo. Integrated Amygdala, Orbitofrontal and Hippocampal Contributions to Reward and Loss Coding Revealed with Human Intracranial EEG. The Journal of neuroscience : the official journal of the Society for Neuroscience. 2022-02-12. PMID:35149513. increased hfg synchronization between the amygdala and hippocampus during reward receipt suggested encoding of reward information into memory for reinstatement during anticipation. 2022-02-12 2023-08-13 human
John G Howland, Rutsuko Ito, Christopher C Lapish, Franz R Villarue. The rodent medial prefrontal cortex and associated circuits in orchestrating adaptive behavior under variable demands. Neuroscience and biobehavioral reviews. 2022-02-08. PMID:35131398. we review the involvement of mpfc subregions, and their projections to the striatum and amygdala in two broad types of tasks in rodents: 1) appetitive and aversive pavlovian and operant conditioning tasks that engage mpfc-striatum and mpfc-amygdala circuits, and 2) foraging-based tasks that require decision making to optimize reward. 2022-02-08 2023-08-13 Not clear
Yan-Yu Wang, Yi Wang, Jia Huang, Xi-He Sun, Xi-Zhen Wang, Shu-Xian Zhang, Guo-Hui Zhu, Simon S Y Lui, Eric F C Cheung, Hong-Wei Sun, Raymond C K Cha. Shared and distinct reward neural mechanisms among patients with schizophrenia, major depressive disorder, and bipolar disorder: an effort-based functional imaging study. European archives of psychiatry and clinical neuroscience. 2022-01-26. PMID:35079855. compared to hc, scz patients exhibited stronger variations of functional connectivity between the right caudate and the left amygdala, the left hippocampus and the left putamen, with increase in reward magnitude. 2022-01-26 2023-08-13 Not clear
Katherine S Young, Camilla Ward, Meghan Vinograd, Kelly Chen, Susan Y Bookheimer, Robin Nusslock, Richard E Zinbarg, Michelle G Crask. Individual differences in threat and reward neural circuitry activation: testing dimensional models of early adversity, anxiety and depression. The European journal of neuroscience. 2022-01-06. PMID:34989038. we examined functional brain activity during a face processing task in threat (amygdala, ventromedial prefrontal cortex) and reward (ventral striatum, orbitofrontal cortex) regions of interest among a sample (n = 103) of young adults (aged 18-19 years) in relation to dimensional measures of early life adversity and symptoms of anxiety and depression. 2022-01-06 2023-08-13 Not clear
Jennifer L Cornish, Asheeta A Prasa. Sex Differences in Substance Use Disorders: A Neurobiological Perspective. Frontiers in global women's health. vol 2. 2021-12-27. PMID:34957467. recent clinical studies in sud analyzing sex differences reveal neurobiological changes that are differentially impacted in common reward processing regions such as the striatum, hippocampus, amygdala, insula, and corpus collosum. 2021-12-27 2023-08-13 Not clear
Rafael Pineda, Encarnacion Torres, Manuel Tena-Semper. Extrahypothalamic Control of Energy Balance and Its Connection with Reproduction: Roles of the Amygdala. Metabolites. vol 11. issue 12. 2021-12-23. PMID:34940594. the aim of this mini-review article is to summarize the most salient experimental data supporting a role of the amygdala as a key brain region for emotional learning and behavior, including reward processing, in the physiological control of feeding and energy balance. 2021-12-23 2023-08-13 Not clear
Siying Li, Frank Krueger, Julia A Camilleri, Simon B Eickhoff, Chen Q. The neural signatures of social hierarchy-related learning and interaction: A coordinate- and connectivity-based meta-analysis. NeuroImage. vol 245. 2021-12-11. PMID:34788662. we identified the anterior insula and temporoparietal junction (dominance detection), medial prefrontal cortex (information updating and computation), and intraparietal sulcus region, amygdala, and hippocampus (social hierarchy representation) as consistent activated brain regions for sh-rl, but the striatum, amygdala, and hippocampus associated with reward processing for sh-ri. 2021-12-11 2023-08-13 Not clear
Ronald Sladky, Federica Riva, Lisa Anna Rosenberger, Jack van Honk, Claus Lam. Basolateral and central amygdala orchestrate how we learn whom to trust. Communications biology. vol 4. issue 1. 2021-12-11. PMID:34824373. this suggests that learning whom to trust is not related to reward processing in the nucleus accumbens, but rather to engagement of the amygdala. our study overcomes major empirical gaps between animal models and human neuroimaging and shows how different subnuclei of the amygdala and connected areas orchestrate learning to form different subjective trustworthiness beliefs about others and guide trust choice behavior. 2021-12-11 2023-08-13 human
Atsushi Fujimoto, Elisabeth A Murray, Peter H Rudebec. Interaction between decision-making and interoceptive representations of bodily arousal in frontal cortex. Proceedings of the National Academy of Sciences of the United States of America. vol 118. issue 35. 2021-12-02. PMID:34452993. applying a population-coding analysis, we show that after bilateral amygdala lesions, the balance of encoding in dacc is skewed away from signaling either reward value or choice direction toward hr coding around the time that choices are made. 2021-12-02 2023-08-13 human
Alexander K Zinsmaier, Yan Dong, Yanhua H Huan. Cocaine-induced projection-specific and cell type-specific adaptations in the nucleus accumbens. Molecular psychiatry. 2021-11-26. PMID:33963288. the nucleus accumbens (nac) integrates and prioritizes different emotional and motivational inputs to the reward system by processing convergent glutamatergic projections from the medial prefrontal cortex, basolateral amygdala, ventral hippocampus, and other limbic and paralimbic brain regions. 2021-11-26 2023-08-13 Not clear
Nina T Lichtenberg, Linnea Sepe-Forrest, Zachary T Pennington, Alexander C Lamparelli, Venuz Y Greenfield, Kate M Wassu. The Medial Orbitofrontal Cortex-Basolateral Amygdala Circuit Regulates the Influence of Reward Cues on Adaptive Behavior and Choice. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 41. issue 34. 2021-11-09. PMID:34272313. the medial orbitofrontal cortex-basolateral amygdala circuit regulates the influence of reward cues on adaptive behavior and choice. 2021-11-09 2023-08-13 rat
Merridee J Lefner, Alexa P Magnon, James M Gutierrez, Matthew R Lopez, Matthew J Wana. Delays to Reward Delivery Enhance the Preference for an Initially Less Desirable Option: Role for the Basolateral Amygdala and Retrosplenial Cortex. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 41. issue 35. 2021-11-09. PMID:34315810. delays to reward delivery enhance the preference for an initially less desirable option: role for the basolateral amygdala and retrosplenial cortex. 2021-11-09 2023-08-13 rat
Merridee J Lefner, Alexa P Magnon, James M Gutierrez, Matthew R Lopez, Matthew J Wana. Delays to Reward Delivery Enhance the Preference for an Initially Less Desirable Option: Role for the Basolateral Amygdala and Retrosplenial Cortex. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 41. issue 35. 2021-11-09. PMID:34315810. our findings demonstrate the basolateral amygdala and retrosplenial cortex are required for temporal delays to enhance the preference for an initially less desirable reward. 2021-11-09 2023-08-13 rat
Shijing Wang, Francesco Leri, Sakina J Rizv. Anhedonia as a central factor in depression: Neural mechanisms revealed from preclinical to clinical evidence. Progress in neuro-psychopharmacology & biological psychiatry. vol 110. 2021-11-01. PMID:33631251. substantial preclinical and clinical research has explored the neural basis of reward deficits in the context of depression, and has implicated mesocorticolimbic reward circuitry comprising the nucleus accumbens, ventral pallidum, ventral tegmental area, amygdala, hippocampus, anterior cingulate, insula, orbitofrontal cortex, and other prefrontal cortex regions. 2021-11-01 2023-08-13 Not clear