All Relations between associative learning and hippocampus

Publication Sentence Publish Date Extraction Date Species
Yanjun Sun, Lisa M Giocom. Neural circuit dynamics of drug-context associative learning in the mouse hippocampus. Nature communications. vol 13. issue 1. 2022-11-07. PMID:36344498. neural circuit dynamics of drug-context associative learning in the mouse hippocampus. 2022-11-07 2023-08-14 mouse
Yanjun Sun, Lisa M Giocom. Neural circuit dynamics of drug-context associative learning in the mouse hippocampus. Nature communications. vol 13. issue 1. 2022-11-07. PMID:36344498. using longitudinal calcium imaging in freely behaving mice, we find that unlike the associative learning of natural reward, drug-context associations for psychostimulants and opioids are encoded in a specific subset of hippocampal neurons. 2022-11-07 2023-08-14 mouse
Salonee V Patel, Courtney M DeCarlo, Shae A Book, Ashley L Schormans, Shawn N Whitehead, Brian L Allman, Sarah H Haye. Noise exposure in early adulthood causes age-dependent and brain region-specific impairments in cognitive function. Frontiers in neuroscience. vol 16. 2022-10-31. PMID:36312027. ultimately, our results suggest that not all higher-level cognitive tasks or their associated brain regions appear to be equally susceptible to noise-induced deficits during aging, as the occupational-like noise exposure caused an age-dependent deficit in spatial but not visuomotor associative learning, as well as altered microglial expression in the hippocampus but not the striatum. 2022-10-31 2023-08-14 human
Rongrong Li, Weiwei Zhang, Jie Zhang, Haibo Zhang, Hui Chen, Zhian Hu, Zhongxiang Yao, Hao Chen, Bo H. Sustained activity of hippocampal parvalbumin-expressing interneurons supports trace eyeblink conditioning in mice. The Journal of neuroscience : the official journal of the Society for Neuroscience. 2022-09-27. PMID:36167784. here, we combined multi-channel recording and optogenetics to elucidate how the hippocampal parvalbumin-expressing interneurons (pv-in) support associative learning. 2022-09-27 2023-08-14 mouse
Rongrong Li, Weiwei Zhang, Jie Zhang, Haibo Zhang, Hui Chen, Zhian Hu, Zhongxiang Yao, Hao Chen, Bo H. Sustained activity of hippocampal parvalbumin-expressing interneurons supports trace eyeblink conditioning in mice. The Journal of neuroscience : the official journal of the Society for Neuroscience. 2022-09-27. PMID:36167784. our current findings highlight the involvement of hippocampal pv-ins in tebc acquisition, and reveal insights into the pv-in activity kinetics which are of key importance for the hippocampal involvement in associative learning. 2022-09-27 2023-08-14 mouse
Yingwei Zheng, Sijue Tao, Yue Liu, Jingjing Liu, Liping Sun, Yawen Zheng, Yu Tian, Peng Su, Xutao Zhu, Fuqiang X. Basal Forebrain-Dorsal Hippocampus Cholinergic Circuit Regulates Olfactory Associative Learning. International journal of molecular sciences. vol 23. issue 15. 2022-08-12. PMID:35955605. basal forebrain-dorsal hippocampus cholinergic circuit regulates olfactory associative learning. 2022-08-12 2023-08-14 Not clear
Benjamin W Corrigan, Roberto A Gulli, Guillaume Doucet, Megan Roussy, Rogelio Luna, Kartik S Pradeepan, Adam J Sachs, Julio C Martinez-Trujill. Distinct neural codes in primate hippocampus and lateral prefrontal cortex during associative learning in virtual environments. Neuron. 2022-05-13. PMID:35561675. distinct neural codes in primate hippocampus and lateral prefrontal cortex during associative learning in virtual environments. 2022-05-13 2023-08-13 Not clear
Theodoros Tsetsenis, Julia K Badyna, Rebecca Li, John A Dan. Activation of a Locus Coeruleus to Dorsal Hippocampus Noradrenergic Circuit Facilitates Associative Learning. Frontiers in cellular neuroscience. vol 16. 2022-05-02. PMID:35496910. activation of a locus coeruleus to dorsal hippocampus noradrenergic circuit facilitates associative learning. 2022-05-02 2023-08-13 Not clear
Hyesang Chang, Lang Chen, Yuan Zhang, Ye Xie, Carlo de Los Angeles, Emma Adair, Gaston Zanitti, Demian Wassermann, Miriam Rosenberg-Lee, Vinod Meno. Foundational number sense training gains are predicted by hippocampal-parietal circuits. The Journal of neuroscience : the official journal of the Society for Neuroscience. 2022-04-12. PMID:35410879. crucially, the strength of pre-training functional connectivity between the hippocampus and intraparietal sulcus, brain regions implicated in associative learning and quantity discrimination, respectively, predicted individual differences in number sense learning across typically developing children and children with learning difficulties. 2022-04-12 2023-08-13 Not clear
Andie Dodge, Nicole Morrill, Edwin J Weeber, Kevin R Nas. Recovery of Angelman syndrome rat deficits with UBE3A protein supplementation. Molecular and cellular neurosciences. 2022-04-03. PMID:35367589. furthermore, injection of recombinant ube3a protein into the hippocampus of the as rat can rescue the associative learning and memory deficits seen in the fear conditioning task. 2022-04-03 2023-08-13 rat
Valerie J Estela-Pro, Rebecca D Burwel. The anatomy and function of the postrhinal cortex. Behavioral neuroscience. 2021-12-16. PMID:34914422. these representations of context are available to be used by multiple brain regions, including prefrontal, posterior cortical, and hippocampal areas, for context-guided behavior, associative learning, and episodic memory. 2021-12-16 2023-08-13 human
Eda Mızrak, Nichole R Bouffard, Laura A Libby, Erie D Boorman, Charan Ranganat. The hippocampus and orbitofrontal cortex jointly represent task structure during memory-guided decision making. Cell reports. vol 37. issue 9. 2021-12-01. PMID:34852232. here, we examine how the human hippocampus and ofc represent task structure during an associative learning task that required learning of both context-determined and context-invariant probabilistic associations. 2021-12-01 2023-08-13 human
Jing Qu, Liyuan Hu, Xiaoyu Liu, Jie Dong, Rui Yang, Leilei Me. The contributions of the left hippocampus and bilateral inferior parietal lobule to form-meaning associative learning. Psychophysiology. vol 58. issue 8. 2021-11-03. PMID:33949705. the contributions of the left hippocampus and bilateral inferior parietal lobule to form-meaning associative learning. 2021-11-03 2023-08-13 Not clear
Jing Qu, Liyuan Hu, Xiaoyu Liu, Jie Dong, Rui Yang, Leilei Me. The contributions of the left hippocampus and bilateral inferior parietal lobule to form-meaning associative learning. Psychophysiology. vol 58. issue 8. 2021-11-03. PMID:33949705. nevertheless, researchers have not clearly determined how the hippocampus and cortical regions dynamically interact during novel word learning, especially during form-meaning associative learning. 2021-11-03 2023-08-13 Not clear
Jing Qu, Liyuan Hu, Xiaoyu Liu, Jie Dong, Rui Yang, Leilei Me. The contributions of the left hippocampus and bilateral inferior parietal lobule to form-meaning associative learning. Psychophysiology. vol 58. issue 8. 2021-11-03. PMID:33949705. as a method to address this question, we used an online learning paradigm and representational similarity analysis to explore the contributions of the hippocampus and neocortex to form-meaning associative learning. 2021-11-03 2023-08-13 Not clear
Jing Qu, Liyuan Hu, Xiaoyu Liu, Jie Dong, Rui Yang, Leilei Me. The contributions of the left hippocampus and bilateral inferior parietal lobule to form-meaning associative learning. Psychophysiology. vol 58. issue 8. 2021-11-03. PMID:33949705. form-meaning associative learning elicited activations in a wide neural network including regions required for word processing (i.e., the bilateral inferior frontal gyrus and the occipitotemporal cortex), regions required for encoding (i.e., the bilateral parahippocampus and hippocampus), and regions required for cognitive control (i.e., the anterior cingulate cortex and dorsolateral prefrontal cortex). 2021-11-03 2023-08-13 Not clear
Jing Qu, Liyuan Hu, Xiaoyu Liu, Jie Dong, Rui Yang, Leilei Me. The contributions of the left hippocampus and bilateral inferior parietal lobule to form-meaning associative learning. Psychophysiology. vol 58. issue 8. 2021-11-03. PMID:33949705. more importantly, our study revealed the differential roles of the left hippocampus and bilateral inferior parietal lobule (ipl) in form-meaning associative learning. 2021-11-03 2023-08-13 Not clear
Jenna L Merenstein, Jessica R Petok, Ilana J Bennet. Age group differences in learning-related activity reflect task stage, not learning stage. Behavioural brain research. vol 416. 2021-10-05. PMID:34499941. previous functional magnetic resonance imaging (fmri) studies have attributed these implicit associative learning (ial) deficits to differential engagement of the hippocampus and basal ganglia in older relative to younger adults in early and late stages of the task, respectively. 2021-10-05 2023-08-13 Not clear
Wei-Wei Zhang, Rong-Rong Li, Jie Zhang, Jie Yan, Qian-Hui Zhang, Zhi-An Hu, Bo Hu, Zhong-Xiang Yao, Hao Che. Hippocampal Interneurons are Required for Trace Eyeblink Conditioning in Mice. Neuroscience bulletin. vol 37. issue 8. 2021-08-18. PMID:33991316. our findings highlight the role of hippocampal interneurons in the tebc, and point to a potential cellular mechanism subserving associative learning. 2021-08-18 2023-08-13 mouse
Shih-Pi Ku, Eric L Hargreaves, Sylvia Wirth, Wendy A Suzuk. The contributions of entorhinal cortex and hippocampus to error driven learning. Communications biology. vol 4. issue 1. 2021-08-09. PMID:34031534. to test this, we recorded in the entorhinal cortex (ec) and hippocampus (hpc) as macaques performed an associative learning task using an error-driven learning strategy, defined as better performance after error relative to correct trials. 2021-08-09 2023-08-13 Not clear