| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Dhairyya Singh, Kenneth A Norman, Anna C Schapir. A model of autonomous interactions between hippocampus and neocortex driving sleep-dependent memory consolidation. Proceedings of the National Academy of Sciences of the United States of America. vol 119. issue 44. 2022-10-24. PMID:36279437. |
many theories of memory formation and consolidation have posited that the hippocampus stores new information, then "teaches" this information to the neocortex over time, especially during sleep. |
2022-10-24 |
2023-08-14 |
Not clear |
| Adrian Aleman-Zapata, Richard G M Morris, Lisa Genze. Sleep deprivation and hippocampal ripple disruption after one-session learning eliminate memory expression the next day. Proceedings of the National Academy of Sciences of the United States of America. vol 119. issue 44. 2022-10-24. PMID:36279444. |
faster cortical high-frequency oscillations increased after normal learning, a change not seen in the hippocampal ripple-disruption condition, consistent with these having a role in memory consolidation. |
2022-10-24 |
2023-08-14 |
Not clear |
| Jessica D Creery, David J Brang, Jason D Arndt, Adrianna Bassard, Vernon L Towle, James X Tao, Shasha Wu, Sandra Rose, Peter C Warnke, Naoum P Issa, Ken A Palle. Electrophysiological markers of memory consolidation in the human brain when memories are reactivated during sleep. Proceedings of the National Academy of Sciences of the United States of America. vol 119. issue 44. 2022-10-24. PMID:36279460. |
for factual or event knowledge, consolidation is thought to progress during sleep as well as during waking states and to be mediated by interactions between hippocampal and neocortical networks. |
2022-10-24 |
2023-08-14 |
human |
| Rafael Pedrosa, Mojtaba Nazari, Majid H Mohajerani, Thomas Knöpfel, Federico Stella, Francesco P Battagli. Hippocampal gamma and sharp wave/ripples mediate bidirectional interactions with cortical networks during sleep. Proceedings of the National Academy of Sciences of the United States of America. vol 119. issue 44. 2022-10-24. PMID:36279469. |
hippocampus-neocortex interactions during sleep are critical for memory processes: hippocampally initiated replay contributes to memory consolidation in the neocortex and hippocampal sharp wave/ripples modulate cortical activity. |
2022-10-24 |
2023-08-14 |
Not clear |
| Rafael Pedrosa, Mojtaba Nazari, Majid H Mohajerani, Thomas Knöpfel, Federico Stella, Francesco P Battagli. Hippocampal gamma and sharp wave/ripples mediate bidirectional interactions with cortical networks during sleep. Proceedings of the National Academy of Sciences of the United States of America. vol 119. issue 44. 2022-10-24. PMID:36279469. |
in fact, neocortical activity predicted hippocampal slow gamma and followed ripples, suggesting that consolidation processes rely on bidirectional signaling between hippocampus and neocortex. |
2022-10-24 |
2023-08-14 |
Not clear |
| Han Qin, Ling Fu, Tingliang Jian, Wenjun Jin, Mengru Liang, Jin Li, Qianwei Chen, Xinyu Yang, Haoran Du, Xiang Liao, Kuan Zhang, Rui Wang, Shanshan Liang, Jiwei Yao, Bo Hu, Shuancheng Ren, Chunqing Zhang, Yanjiang Wang, Zhian Hu, Hongbo Jia, Arthur Konnerth, Xiaowei Che. REM sleep-active hypothalamic neurons may contribute to hippocampal social-memory consolidation. Neuron. 2022-10-22. PMID:36272414. |
rem sleep-active hypothalamic neurons may contribute to hippocampal social-memory consolidation. |
2022-10-22 |
2023-08-14 |
mouse |
| Jessica Rosa, Jociane de Carvalho Myskiw, Natalia Gindri Fiorenza, Cristiane Regina Guerino Furini, Gerson Guilherme Sapiras, Ivan Izquierd. Hippocampal cholinergic receptors and the mTOR participation in fear-motivated inhibitory avoidance extinction memory. Behavioural brain research. 2022-09-30. PMID:36179804. |
this study provides insights related to the behavioural aspects and the neurobiological properties underlying the early stage of fear-motivated ia extinction memory consolidation and suggests that there is hippocampal muscarinic receptor participation independent of mtor in this memory process. |
2022-09-30 |
2023-08-14 |
rat |
| Jake Valeri, Sinead M O'Donovan, Wei Wang, David Sinclair, Ratna Bollavarapu, Barbara Gisabella, Donna Platt, Craig Stockmeier, Harry Pantazopoulo. Altered expression of somatostatin signaling molecules and clock genes in the hippocampus of subjects with substance use disorder. Frontiers in neuroscience. vol 16. 2022-09-26. PMID:36161151. |
hippocampal somatostatin signaling is involved in encoding and consolidation of contextual memories which contribute to relapse in substance use disorder. |
2022-09-26 |
2023-08-14 |
human |
| Catherine W Tallman, Robert E Clark, Christine N Smit. A way forward for design and analysis of neuroimaging studies of memory consolidation. Cognitive neuroscience. 2022-09-16. PMID:36112016. |
careful consideration of the content and context of memory while accounting for the neuroanatomy and functional specialization of the hippocampus may reveal more consistent patterns in fmri studies of memory consolidation. |
2022-09-16 |
2023-08-14 |
Not clear |
| Xu Tan, Xiaoyu Liu, E Liu, Min Liu, Shouhong Mu, Zhaofang Hang, Weikai Han, Tingting Wang, Yang Zhang, Jing Zhang, Qingwei Yue, Jinhao Su. Astrocyte-derived lactate/NADH alters methamphetamine-induced memory consolidation and retrieval by regulating neuronal synaptic plasticity in the dorsal hippocampus. Brain structure & function. 2022-09-16. PMID:36112231. |
astrocyte-derived lactate/nadh alters methamphetamine-induced memory consolidation and retrieval by regulating neuronal synaptic plasticity in the dorsal hippocampus. |
2022-09-16 |
2023-08-14 |
mouse |
| Tsukasa Funane, Heechul Jun, Stephanie Sutoko, Takaomi C Saido, Akihiko Kandori, Kei M Igarash. Impaired sharp-wave ripple coordination between the medial entorhinal cortex and hippocampal CA1 of knock-in model of Alzheimer's disease. Frontiers in systems neuroscience. vol 16. 2022-09-12. PMID:36090186. |
in healthy brains, sharp-wave ripples (swrs) in the hippocampus and entorhinal cortex play a critical role in memory consolidation. |
2022-09-12 |
2023-08-14 |
mouse |
| Charles W Dickey, Ilya A Verzhbinsky, Xi Jiang, Burke Q Rosen, Sophie Kajfez, Emad N Eskandar, Jorge Gonzalez-Martinez, Sydney S Cash, Eric Halgre. Cortical ripples during NREM sleep and waking in humans. The Journal of neuroscience : the official journal of the Society for Neuroscience. 2022-08-30. PMID:36041852. |
hippocampal ripples index the reconstruction of spatiotemporal neuronal firing patterns essential for the consolidation of memories in the cortex during non-rapid eye movement sleep (nrem). |
2022-08-30 |
2023-08-14 |
human |
| Rachel A Swanson, Daniel Levenstein, Kathryn McClain, David Tingley, György Buzsák. Variable specificity of memory trace reactivation during hippocampal sharp wave ripples. Current opinion in behavioral sciences. vol 32. 2022-08-29. PMID:36034494. |
hippocampal sharp wave-ripples (swr) are thought to mediate brain-wide reactivation of memory traces in service of memory consolidation. |
2022-08-29 |
2023-08-14 |
Not clear |
| Zhiqian Yu, Mai Sakai, Hotaka Fukushima, Chiaki Ono, Yoshie Kikuchi, Ryuta Koyama, Ko Matsui, Tomoyuki Furuyashiki, Satoshi Kida, Hiroaki Tomit. Contextual fear conditioning regulates synapse-related gene transcription in mouse microglia. Brain research bulletin. 2022-08-20. PMID:35987296. |
furthermore, in the hippocampal microglia, we found that the expression of neurotransmitter release regulators, γ-aminobutyric acid (gaba) receptor gabrb3 and synapsin 1/2, increased under fear memory consolidation and restored (decreased) after extinction. |
2022-08-20 |
2023-08-14 |
mouse |
| Xin Yang, Ru Gong, Linwei Qin, Yifei Bao, Yi Fu, Shan Gao, Hui Yang, Jinfei Ni, Ti-Fei Yuan, Wei L. Trafficking of NMDA receptors is essential for hippocampal synaptic plasticity and memory consolidation. Cell reports. vol 40. issue 7. 2022-08-17. PMID:35977502. |
trafficking of nmda receptors is essential for hippocampal synaptic plasticity and memory consolidation. |
2022-08-17 |
2023-08-14 |
rat |
| Anuck Sawangjit, Maximilian Harkotte, Carlos N Oyanedel, Niels Niethard, Jan Born, Marion Inostroz. Two distinct ways to form long-term object recognition memory during sleep and wakefulness. Proceedings of the National Academy of Sciences of the United States of America. vol 119. issue 34. 2022-08-15. PMID:35969775. |
our findings indicate two distinct modes of long-term memory formation: sleep consolidation is hippocampus dependent and implicates event-context binding, whereas wake consolidation is impaired by hippocampal activation and strengthens context-independent representations. |
2022-08-15 |
2023-08-14 |
rat |
| Zahra Alizadeh, Amin Azimi, Maryam Ghorban. Enhancement of hippocampal-thalamocortical temporal coordination during slow-frequency long-duration anterior thalamic spindles. The Journal of neuroscience : the official journal of the Society for Neuroscience. 2022-08-15. PMID:35970563. |
temporal nesting of cortical slow oscillations (so), thalamic spindles and hippocampal ripples indicates multi-regional neuronal interactions required for memory consolidation. |
2022-08-15 |
2023-08-14 |
mouse |
| Karola Kaefer, Federico Stella, Bruce L McNaughton, Francesco P Battagli. Replay, the default mode network and the cascaded memory systems model. Nature reviews. Neuroscience. 2022-08-15. PMID:35970912. |
in the 'cascaded memory systems model' that we outline here, we hypothesize that the dmn forms the backbone for the propagation of replay, mediating interactions between the hippocampus and the neocortex that enable the consolidation of new memories. |
2022-08-15 |
2023-08-14 |
Not clear |
| Kathryn N Graves, Brynn E Sherman, David Huberdeau, Eyiyemisi Damisah, Imran H Quraishi, Nicholas B Turk-Brown. Remembering the pattern: A longitudinal case study on statistical learning in spatial navigation and memory consolidation. Neuropsychologia. 2022-08-12. PMID:35961387. |
taken together, these findings suggest that the hippocampus may contribute to the initial extraction of regularities prior to cortical consolidation. |
2022-08-12 |
2023-08-14 |
Not clear |
| Elena I Zakharova, Andrey T Proshin, Mikhail Y Monakov, Alexander M Dudchenk. Cholinergic Internal and Projection Systems of Hippocampus and Neocortex Critical for Early Spatial Memory Consolidation in Normal and Chronic Cerebral Hypoperfusion Conditions in Rats with Different Abilities to Consolidation: The Role of Cholinergic Interneurons of the Hippocampus. Biomedicines. vol 10. issue 7. 2022-07-27. PMID:35884837. |
cholinergic internal and projection systems of hippocampus and neocortex critical for early spatial memory consolidation in normal and chronic cerebral hypoperfusion conditions in rats with different abilities to consolidation: the role of cholinergic interneurons of the hippocampus. |
2022-07-27 |
2023-08-14 |
human |