All Relations between reward and amygdala

Publication Sentence Publish Date Extraction Date Species
Tatiane Ferreira Tavares, José Lino Oliveira Bueno, Valérie Doyèr. Temporal prediction error triggers amygdala-dependent memory updating in appetitive operant conditioning in rats. Frontiers in behavioral neuroscience. vol 16. 2023-01-27. PMID:36703723. experiment 2 showed that negative prediction errors, either due to the temporal change or through reward omission, increased in the basolateral amygdala nucleus (bla) the activation of a protein that is critical for memory formation. 2023-01-27 2023-08-14 rat
Josue M Avecillas-Chasin, Simon Levinson, Taylor Kuhn, Mahmoud Omidbeigi, Jean-Philippe Langevin, Nader Pouratian, Ausaf Bar. Connectivity-based parcellation of the amygdala and identification of its main white matter connections. Scientific reports. vol 13. issue 1. 2023-01-24. PMID:36693904. using probabilistic tractography, we created population statistical maps of amygdala connectivity to brain regions involved in limbic, associative, memory, and reward circuits. based on the amygdala connectivity with these regions, we applied k-means clustering to parcellate the amygdala into three clusters. 2023-01-24 2023-08-14 human
Josue M Avecillas-Chasin, Simon Levinson, Taylor Kuhn, Mahmoud Omidbeigi, Jean-Philippe Langevin, Nader Pouratian, Ausaf Bar. Connectivity-based parcellation of the amygdala and identification of its main white matter connections. Scientific reports. vol 13. issue 1. 2023-01-24. PMID:36693904. this in vivo connectivity-based parcellation of the amygdala delineates three clusters of the amygdala in a mediolateral pattern based on its connectivity with brain areas involved in cognition, memory, emotion, and reward. 2023-01-24 2023-08-14 human
Antonio Bernal, María A Zafra, María J Simón, Javier Mahí. Sodium Homeostasis, a Balance Necessary for Life. Nutrients. vol 15. issue 2. 2023-01-21. PMID:36678265. circuits are formed that stimulate or inhibit homeostatic na intake involving participation of the parabrachial nucleus, pre-locus coeruleus, medial tuberomammillary nuclei, median eminence, paraventricular and supraoptic nuclei, and other structures with reward properties such as the bed nucleus of the stria terminalis, central amygdala, and ventral tegmental area. 2023-01-21 2023-08-14 Not clear
Shaoqiang Han, Ruiping Zheng, Shuying Li, Bingqian Zhou, Yu Jiang, Keke Fang, Yarui Wei, Baohong Wen, Jianyue Pang, Hengfen Li, Yong Zhang, Yuan Chen, Jingliang Chen. Altered structural covariance network of nucleus accumbens is modulated by illness duration and severity of symptom in depression. Journal of affective disorders. vol 324. 2023-01-07. PMID:36608848. patients with depression exhibited altered structural covariance of nacc connected to key brain regions in reward system including the medial orbitofrontal cortex, amygdala, insula, parahippocampa gyrus, precuneus, thalamus, hippocampus and cerebellum. 2023-01-07 2023-08-14 human
Laura C Ornelas, Giorgia Boero, Kalynn Van Voorhies, Todd K O'Buckley, Joyce Besheer, A Leslie Morro. Pharmacological administration of 3α,5α-THP into nucleus accumbens core increases 3α,5α-THP expression and reduces alcohol self-administration. Alcoholism, clinical and experimental research. 2023-01-01. PMID:36587947. alcohol affects multiple circuits in the brain, mainly disrupting the delicate balance between inhibitory γ-aminobutyric acid (gaba) transmission and excitatory glutamate signaling in brain areas involved in reward circuits, such as amygdala, nucleus accumbens (acb) and ventral tegmental area (vta), causing loss of control in circuits that regulate behavioral control of craving, alcohol-seeking and intake. 2023-01-01 2023-08-14 human
Yu-Chen Chan, Tai-Li Cho. Effective connectivity of the amygdala during the consumption of erotic, sexual humor, and monetary rewards with a DCM-PEB approach. PloS one. vol 17. issue 12. 2022-12-29. PMID:36580445. the amygdala, nac, and lofc are major dopaminergic targets with known roles in the reward circuitry. 2022-12-29 2023-08-14 Not clear
Honoreé W Brewton, Stacey L Robinson, Todd E Thiel. Astrocyte Expression in the Extended Amygdala of C57BL/6J Mice is Sex-Dependently Affected by Chronic Intermittent and Binge-Like Ethanol Exposure. Alcohol (Fayetteville, N.Y.). 2022-12-20. PMID:36539069. the basolateral amygdala (bla), central amygdala (cea), and bed nucleus of the stria terminalis (bnst) are brain regions that process stress, anxiety, and reward; they are also implicated in modulating ethanol intake. 2022-12-20 2023-08-14 mouse
Minjie Huang, Guoqing Wang, Yazhou Lin, Yanyan Guo, Xiuhua Ren, Jinping Shao, Jing Cao, Weidong Zang, Zhihua L. Dopamine receptor D2, but not D1, mediates the reward circuit from the ventral tegmental area to the central amygdala, which is involved in pain relief. Molecular pain. 2022-12-04. PMID:36464669. dopamine receptor d2, but not d1, mediates the reward circuit from the ventral tegmental area to the central amygdala, which is involved in pain relief. 2022-12-04 2023-08-14 mouse
Minjie Huang, Guoqing Wang, Yazhou Lin, Yanyan Guo, Xiuhua Ren, Jinping Shao, Jing Cao, Weidong Zang, Zhihua L. Dopamine receptor D2, but not D1, mediates the reward circuit from the ventral tegmental area to the central amygdala, which is involved in pain relief. Molecular pain. 2022-12-04. PMID:36464669. whether the reward circuit from the ventral tegmental area (vta) to the central amygdala (cea) is involved in pain relief remains unexplored. 2022-12-04 2023-08-14 mouse
Kathryn R Hill, David T Hsu, Stephan F Taylor, R Todd Ogden, Ramin V Parsey, Christine DeLorenz. Mu Opioid Receptor Dynamics in Healthy Volunteers with a History of Childhood Maltreatment. Journal of child & adolescent trauma. vol 15. issue 4. 2022-11-28. PMID:36439668. the mu opioid receptor rich nucleus accumbens and amygdala are critical to reward and stress processing respectively. 2022-11-28 2023-08-14 human
Sai Sun, Chuhua Cai, Rongjun Y. Behavioral and neural representation of expected reward and risk. NeuroImage. vol 264. 2022-11-10. PMID:36356436. the positive striatal connectivity to the amygdala and negative striatal connectivity to the superior frontal gyrus were correlated with individuals' sensitivity to the expected reward. 2022-11-10 2023-08-14 human
Peter M Kaskan, Mark A Nicholas, Aaron M Dean, Elisabeth A Murra. Attention to stimuli of learned versus innate biological value rely on separate neural systems. The Journal of neuroscience : the official journal of the Society for Neuroscience. 2022-11-01. PMID:36319119. because the amygdala plays a role in reward processing, and the activity of amygdala neurons has been linked to spatial attention, we reasoned that the amygdala may be essential for attending to rewarded images. 2022-11-01 2023-08-14 human
Keishi Okamoto, Satoshi Tanaka, Yasutaka Suzuki, Takashi Shigematsu, Kenjiro Kunieda, Kyoko Hojo, Akio Shimizu, Tomohisa Ohno, Ichiro Fujishim. Food appearance affects reward-related brain activity in healthy adults: a functional magnetic resonance imaging study. International journal of food sciences and nutrition. 2022-10-27. PMID:36300275. compared with pureed foods and non-food objects, ieat® foods showed significantly greater activation in regions of the brain reward system, such as the amygdala, ventral striatum and orbital frontal cortex. 2022-10-27 2023-08-14 Not clear
Nikki Leeuwis, Tom van Bommel, Maryam Alimardan. A framework for application of consumer neuroscience in pro-environmental behavior change interventions. Frontiers in human neuroscience. vol 16. 2022-10-03. PMID:36188183. motivating behavior with reward or punishment will most likely get users engaged in climate change action via brain structures related to the reward system, such as the amygdala, nucleus accumbens, and (pre)frontal cortex, where the reward information and subsequent affective responses are encoded. 2022-10-03 2023-08-14 Not clear
Deena M Walker, Xianxiao Zhou, Ashley M Cunningham, Aarthi Ramakrishnan, Hannah M Cates, Casey K Lardner, Catherine J Peña, Rosemary C Bagot, Orna Issler, Yentl Van der Zee, Andrew P Lipschultz, Arthur Godino, Caleb J Browne, Georgia E Hodes, Eric M Parise, Angelica Torres-Berrio, Pamela J Kennedy, Li Shen, Bin Zhang, Eric J Nestle. Crystallin Mu in Medial Amygdala Mediates the Effect of Social Experience on Cocaine Seeking in Males but Not in Females. Biological psychiatry. 2022-10-01. PMID:36182529. the medial amygdala (mea) is a likely candidate for the modulation of social influence on drug reward because it regulates social reward, develops during adolescence, and is sensitive to social stress. 2022-10-01 2023-08-14 Not clear
Shuyi Qian, Cuijie Shi, Shihao Huang, Chang Yang, Yixiao Lu. DNA methyltransferase activity in the basolateral amygdala is critical for reconsolidation of a heroin reward memory. Frontiers in molecular neuroscience. vol 15. 2022-09-30. PMID:36176958. dna methyltransferase activity in the basolateral amygdala is critical for reconsolidation of a heroin reward memory. 2022-09-30 2023-08-14 Not clear
Marques Jackson, Brittany L Foret, Jane Fontenot, Dana Hasselschwert, Josh Smith, Emily Romero, Karen Müller Smit. Molecular examination of the endogenous opioid system in rhesus macaque monkeys with self-injurious behavior. Journal of neuroscience research. 2022-09-22. PMID:36131680. the brain regions examined are linked to reward reinforcement and stress adaptation including the hypothalamus, orbital frontal cortex, nucleus accumbens, hippocampus, caudate, and the amygdala. 2022-09-22 2023-08-14 human
b' Cec\\xc3\\xadlia Pardo-Bellver, Manuel E Vila-Martin, Sergio Mart\\xc3\\xadnez-Bellver, Mar\\xc3\\xada Villafranca-Faus, Anna Teruel-Sanchis, Camila A Savarelli-Balsamo, Sylwia M Drabik, Joana Mart\\xc3\\xadnez-Ric\\xc3\\xb3s, Ana Cervera-Ferri, Fernando Mart\\xc3\\xadnez-Garc\\xc3\\xada, Enrique Lanuza, Vicent Teruel-Mart\\xc3\\xa. Neural activity patterns in the chemosensory network encoding vomeronasal and olfactory information in mice. Frontiers in neuroanatomy. vol 16. 2022-09-19. PMID:36120099.' no differential c-fos expression was found in the reward system and the basolateral amygdala. 2022-09-19 2023-08-14 mouse
Huiling Yu, Liping Chen, Huiyang Lei, Guilin Pi, Rui Xiong, Tao Jiang, Dongqin Wu, Fei Sun, Yang Gao, Yuanhao Li, Wenju Peng, Bingyu Huang, Guoda Song, Xin Wang, Jingru Lv, Zetao Jin, Dan Ke, Ying Yang, Jian-Zhi Wan. Infralimbic medial prefrontal cortex signalling to calbindin 1 positive neurons in posterior basolateral amygdala suppresses anxiety- and depression-like behaviours. Nature communications. vol 13. issue 1. 2022-09-17. PMID:36115848. here, we found a robust activation of calbindin 1-neurons (calb 1) in the posterior basolateral amygdala (pbla), simultaneous with reward generalization to an ambiguous cue after reward conditioning in mice. 2022-09-17 2023-08-14 mouse