All Relations between consolidation and hippocampus

Publication Sentence Publish Date Extraction Date Species
Josef H L P Sadowski, Matthew W Jones, Jack R Mello. Sharp-Wave Ripples Orchestrate the Induction of Synaptic Plasticity during Reactivation of Place Cell Firing Patterns in the Hippocampus. Cell reports. vol 14. issue 8. 2016-12-13. PMID:26904941. place cell firing patterns reactivated during hippocampal sharp-wave ripples (swrs) in rest or sleep are thought to induce synaptic plasticity and thereby promote the consolidation of recently encoded information. 2016-12-13 2023-08-13 rat
Josef H L P Sadowski, Matthew W Jones, Jack R Mello. Sharp-Wave Ripples Orchestrate the Induction of Synaptic Plasticity during Reactivation of Place Cell Firing Patterns in the Hippocampus. Cell reports. vol 14. issue 8. 2016-12-13. PMID:26904941. our findings confirm an important role for swrs in triggering and tuning plasticity processes that underlie memory consolidation in the hippocampus during rest or sleep. 2016-12-13 2023-08-13 rat
Daniel Bendor, Hugo J Spier. Does the Hippocampus Map Out the Future? Trends in cognitive sciences. vol 20. issue 3. 2016-11-14. PMID:26830730. decades of research have established two central roles of the hippocampus--memory consolidation and spatial navigation. 2016-11-14 2023-08-13 Not clear
Pâmela B Mello-Carpes, Liane da Silva de Vargas, Mateus Cristofari Gayer, Rafael Roehrs, Ivan Izquierd. Hippocampal noradrenergic activation is necessary for object recognition memory consolidation and can promote BDNF increase and memory persistence. Neurobiology of learning and memory. vol 127. 2016-10-19. PMID:26691781. hippocampal noradrenergic activation is necessary for object recognition memory consolidation and can promote bdnf increase and memory persistence. 2016-10-19 2023-08-13 Not clear
Pâmela B Mello-Carpes, Liane da Silva de Vargas, Mateus Cristofari Gayer, Rafael Roehrs, Ivan Izquierd. Hippocampal noradrenergic activation is necessary for object recognition memory consolidation and can promote BDNF increase and memory persistence. Neurobiology of learning and memory. vol 127. 2016-10-19. PMID:26691781. previously we showed that activation of the nucleus of the solitary tract (nts)-nucleus paragigantocellularis (pgi)-locus coeruleus (lc) pathway, which theoretically culminates with norepinephrine (ne) release in dorsal hippocampus (ca1 region) and basolateral amygdala (bla) is necessary for the consolidation of object recognition (or) memory. 2016-10-19 2023-08-13 Not clear
Pâmela B Mello-Carpes, Liane da Silva de Vargas, Mateus Cristofari Gayer, Rafael Roehrs, Ivan Izquierd. Hippocampal noradrenergic activation is necessary for object recognition memory consolidation and can promote BDNF increase and memory persistence. Neurobiology of learning and memory. vol 127. 2016-10-19. PMID:26691781. further, we show that or consolidation is attended by an increase of norepinephrine (ne) levels and of the expression of brain derived neurotrophic factor (bdnf) in hippocampus, which are impaired by inactivation of the nts-pgi-lc pathway by the infusion of muscimol into the nts. 2016-10-19 2023-08-13 Not clear
Sunetra Sase, Ajinkya Sase, Fernando J Sialana, Marion Gröger, Keiryn L Bennett, Oliver Stork, Gert Lubec, Lin L. Individual phases of contextual fear conditioning differentially modulate dorsal and ventral hippocampal GluA1-3, GluN1-containing receptor complexes and subunits. Hippocampus. vol 25. issue 12. 2016-10-13. PMID:25914080. in contextual fear conditioning (cfc), the use of pharmacological and lesion approaches has helped to understand that there are differential roles for the dorsal hippocampus (dh) and the ventral hippocampus (vh) in the acquisition, consolidation and retrieval phases. 2016-10-13 2023-08-13 mouse
Mary L Huff, Eric B Emmons, Nandakumar S Narayanan, Ryan T LaLumier. Basolateral amygdala projections to ventral hippocampus modulate the consolidation of footshock, but not contextual, learning in rats. Learning & memory (Cold Spring Harbor, N.Y.). vol 23. issue 2. 2016-10-12. PMID:26773098. basolateral amygdala projections to ventral hippocampus modulate the consolidation of footshock, but not contextual, learning in rats. 2016-10-12 2023-08-13 rat
Mary L Huff, Eric B Emmons, Nandakumar S Narayanan, Ryan T LaLumier. Basolateral amygdala projections to ventral hippocampus modulate the consolidation of footshock, but not contextual, learning in rats. Learning & memory (Cold Spring Harbor, N.Y.). vol 23. issue 2. 2016-10-12. PMID:26773098. the ventral hippocampus (vh), an efferent target of the bla, has been suggested to selectively process emotion-related learning, yet whether the bla → vh pathway modulates memory consolidation, and does so in a learning-specific manner, is unknown. 2016-10-12 2023-08-13 rat
Q Long, Y Hei, Q Luo, Y Tian, J Yang, J Li, L Wei, W Li. BMSCs transplantation improves cognitive impairment via up-regulation of hippocampal GABAergic system in a rat model of chronic cerebral hypoperfusion. Neuroscience. vol 311. 2016-09-14. PMID:26545982. it is considered that the hippocampus holds the capabilities of memory consolidation and spatial navigation, and the gamma amino butyric acid (gaba)ergic system plays an important role in the control of learning and memory processes. 2016-09-14 2023-08-13 rat
Anna Maslarova, Kristina Lippmann, Seda Salar, Anton Rösler, Uwe Heineman. Differential participation of pyramidal cells in generation of spontaneous sharp wave-ripples in the mouse subiculum in vitro. Neurobiology of learning and memory. vol 125. 2016-09-09. PMID:26318491. previously stored information in the hippocampus is believed to be replayed during sharp wave-ripple activity thereby serving transfer of information from hippocampal areas ca3 and ca1 to the cortical mantle and memory consolidation. 2016-09-09 2023-08-13 mouse
Kasia Radwanska, Grace Schenatto-Pereira, Magdalena Ziółkowska, Kacper Łukasiewicz, K Peter Gies. Mapping fear memory consolidation and extinction-specific expression of JunB. Neurobiology of learning and memory. vol 125. 2016-09-09. PMID:26318493. we found that contextual fear memory consolidation induced junb expression in the medial nucleus and intercalated cells of the amygdala while extinction training induced junb in the ca1 and ca3 areas of the dorsal hippocampus. 2016-09-09 2023-08-13 mouse
Kasia Radwanska, Grace Schenatto-Pereira, Magdalena Ziółkowska, Kacper Łukasiewicz, K Peter Gies. Mapping fear memory consolidation and extinction-specific expression of JunB. Neurobiology of learning and memory. vol 125. 2016-09-09. PMID:26318493. thus, our data suggest that junb expression in the medial nucleus and intercalated cells of the amygdala is involved in fear memory consolidation while alphacamkii-autophosphorylation-dependent junb expression in the areas ca1 and ca3 of the dorsal hippocampus regulates fear memory extinction. 2016-09-09 2023-08-13 mouse
Yina Wei, Giri P Krishnan, Maxim Bazheno. Synaptic Mechanisms of Memory Consolidation during Sleep Slow Oscillations. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 36. issue 15. 2016-09-08. PMID:27076422. our study proposes a neuronal mechanism on how an interaction between hippocampal input, such as mediated by sharp wave-ripple events, cortical slow oscillations, and synaptic plasticity, may lead to consolidation of memories through preferential replay of cortical cell spike sequences during slow-wave sleep. 2016-09-08 2023-08-13 Not clear
Christoph Anacker, Christine Ann Denny, René He. Regulation of hippocampal memory traces by neurogenesis. Neurogenesis (Austin, Tex.). vol 2. issue 1. 2016-09-08. PMID:27604158. recent technological advances of cellular tracing techniques and optogenetic manipulation strategies have allowed to unravel important aspects of the cellular origin of memory, and have started to shed new light on the neuronal networks involved in encoding, consolidation and retrieval of memory in the hippocampus. 2016-09-08 2023-08-13 Not clear
Raphael Koster, Marc Guitart-Masip, Raymond J Dolan, Emrah Düze. Basal Ganglia Activity Mirrors a Benefit of Action and Reward on Long-Lasting Event Memory. Cerebral cortex (New York, N.Y. : 1991). vol 25. issue 12. 2016-08-18. PMID:26420783. the findings indicate a novel type of functional division between the hippocampus and the basal ganglia in the motivational regulation of long-term memory consolidation, which favors remembering events that are worth acting for. 2016-08-18 2023-08-13 Not clear
Jian Zheng, Fei Luo, Nan-nan Guo, Zong-yue Cheng, Bao-ming L. β1-and β2-adrenoceptors in hippocampal CA3 region are required for long-term memory consolidation in rats. Brain research. vol 1627. 2016-08-17. PMID:26343545. taken together, the results suggested that the β1- and β2-ars in the ca3 region were involved in hippocampus dependent memory consolidation. 2016-08-17 2023-08-13 rat
Maryam Sardari, Ameneh Rezayof, Fariba Khodaghol. Hippocampal signaling pathways are involved in stress-induced impairment of memory formation in rats. Brain research. vol 1625. 2016-08-15. PMID:26301822. in addition, stress-induced impairment of memory consolidation or retrieval was associated with the decrease in the p-creb/creb ratio and the pgc-1α level in the hippocampus. 2016-08-15 2023-08-13 rat
Maryam Sardari, Ameneh Rezayof, Fariba Khodaghol. Hippocampal signaling pathways are involved in stress-induced impairment of memory formation in rats. Brain research. vol 1625. 2016-08-15. PMID:26301822. the increased hippocampal levels of nrf2 and it׳s downstream was observed during memory retrieval, while stress-induced impairment of memory consolidation or retrieval inhibited this hippocampal signaling pathway. 2016-08-15 2023-08-13 rat
Melanie Laßek, Jens Weingarten, Martin Wegner, Benjamin F Mueller, Marion Rohmer, Dominic Baeumlisberger, Tabiwang N Arrey, Meike Hick, Jörg Ackermann, Amparo Acker-Palmer, Ina Koch, Ulrike Müller, Michael Karas, Walter Volknand. APP Is a Context-Sensitive Regulator of the Hippocampal Presynaptic Active Zone. PLoS computational biology. vol 12. issue 4. 2016-08-15. PMID:27092780. the pathogenesis involves a successive loss of hippocampal neurons accompanied by a decline in learning and memory consolidation mainly attributed to an accumulation of senile plaques. 2016-08-15 2023-08-13 mouse