Posterior parietal cortex and long-term memory: some data from laboratory animals
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The posterior parietal cortex (PPC) was long viewed as just involved in the perception of spatial relationships between the body and its surroundings and of movements related to them. In recent years the PPC has been shown to participate in many other cognitive processes, among which working memory and the consolidation and retrieval of episodic memory. The neurotransmitter and other molecular processes involved have been determined to a degree in rodents. More research will no doubt determine the extent to which these findings can be extrapolated to primates, including humans. In these there appears to be a paradox: imaging studies strongly suggest an important participation of the PPC in episodic memory, whereas lesion studies are much less suggestive, let alone conclusive. The data on the participation of the PPC in episodic memory so far do not permit any conclusion as to what aspect of consolidation and retrieval it handles in addition to those dealt with by the hippocampus and basolateral amygdala, if any.
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Posterior parietal cortex activations have consistently been observed during episodic retrieval tasks.
“Posterior parietal cortex activations have consistently been observed during episodic retrieval tasks (Hutchinson et al., 2009; Myskiw and Izquierdo, 2012).”
From Neural Correlates of Long-Term Memory Enhancement Following Retrieval Practice (2021) · cites this paper as Myskiw and Izquierdo, 2012
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Sestieri, C., Corbetta, M., Romani, G. L., & Shulman, G. L. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.3335-10.2011 · Cited by 523 · see citing works
Hutchinson, J. B., Uncapher, M. R., & Wagner, A. D. (2009) · Learning & Memory · doi:10.1101/lm.919109 · Cited by 277 · cited 1× · see citing works
“Participation of the PPC in long-term episodic memory began to be realized rather recently and has so far been specifically studied by few groups (Rogers and Kesner, 2007; Berryhill et al., 2007, 2010a,b; Keene and Bucci, 2008; Hutchinson et al., 2009; Drowos et al., 2010).”
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- Alonso M. Bekinschtein P. Cammarota M. Vianna M. R. Izquierdo I. Medina J. H. (2005). Endogenous BDNF is required for long-term memory formation in the rat parietal cortex. Learn. Mem. 12, 504– 610 10.1101/lm.27305 16204202 PMC1240062 · DOI
- Alonso M. Viola H. Izquierdo I. Medina J. H. (2002). Aversive experiences are associated with a rapid and transient activation of ERKs in the rat hippocampus. Neurobiol. Learn. Mem. 77, 119– 124 10.1006/nlme.2000.4000 11749089 · DOI
- Ardenghi P. Barros D. Izquierdo L. A. Bevilaqua L. Schröder N. Quevedo J. Rodrigues C. Madruga M. Medina J. H. Izquierdo I. (1997). Late and prolonged post-training memory modulation in entorhinal and parietal cortex by drugs acting on the cAMP/protein kinase A signaling pathway. Behav. Pharmacol. 8, 745– 751 9832961
- Aujla H. Beninger R. J. (2001). Hippocampal-prefrontocortical cir-cuits: PKA inhibition in the prefrontal cortex impairs delayed nonmatching in the radial maze in rats. Behav. Neurosci. 115, 1204– 1211 11770052
- Barros D. M. Izquierdo L. A. Mello e Souza T. Ardenghi P. G. Pereira P. Medina J. H. Izquierdo I. (2000). Molecular signaling pathways in the cerebral cortex are required for retrieval of one-trial avoidance learning in rats. Behav. Brain Res. 114, 183– 192 10.1016/S0166-4328(00)00226-6 10996059 · DOI
- Barros D. M. Izquierdo L. A. Quevedo J. Rodrigues C. Madruga M. Medina J. H. Izquierdo I. (1998). Interaction between midazolam-induced anterograde amnesia and memory enhancement by treatments given hours later in hippocampus, entorhinal cortex or posterior parietal cortex. Behav. Pharmacol. 92, 163– 167 10.1016/S0166-4328(00)00226-6 10065935 · DOI
- Barros D. M. Mello e Souza T. De David T. Choi H. Aguzzoli A. Madche C. Ardenghi P. Medina J. H. Izquierdo I. (2001). Simultaneous modulation of retrieval by dopaminergic D(1), beta-noradrenergic, serotonergic-1A and cholinergic muscarinic receptors in cortical structures of the rat. Behav. Brain Res. 124, 1– 7 11423160
- Barros D. M. Ramirez M. R. Izquierdo I. (2005). Modulation of working, short- and long-term memory by nicotinic receptors in the basolateral amygdala in rats. Neurobiol. Learn. Mem. 83, 113– 118 10.1016/j.nlm.2004.10.001 15721794 · DOI
- Bekinschtein P. Cammarota M. Igaz L. M. Bevilaqua L. R. M. Izquierdo I. Medina J. H. (2007). Persistence of long-term memory storage requires a late protein synthesis- and BDNF-dependent phase in the hippocampus. Neuron 53, 261– 267 10.1016/j.neuron.2006.11.025 17224407 · DOI · Paper page
- Berryhill M. E. Chein J. Olson I. R. (2011). At the intersection of attention and memory: the mechanistic role of the posterior parietal lobe in working memory. Neuropsychologia 49, 1306– 1315 10.1016/j.neuropsychologia.2011.02.033 21345344 PMC3078173 · DOI
- Berryhill M. E. Phuong L. Picasso L. Cabeza R. Olson I. R. (2007). Parietal lobe and episodic memory: bilateral damage causes impaired free recall of autobiographical memory. J. Neurosci. 27, 14415– 14423 10.1523/JNEUROSCI.4163-07.2007 18160649 PMC6673454 · DOI
- Berryhill M. E. Picasso L. Arnold R. Drowos D. Olson I. R. (2010a). Similarities and differences between parietal and frontal patients in autobiographical and constructed experience tasks. Neuropsychologia 48, 1385– 1393 10.1016/j.neuropsychologia.2010.01.004 20096710 PMC2843776 · DOI
- Berryhill M. E. Wencil E. B. Branch Coslett H. Olson I. R. (2010b). A selective working memory impairment after transcranial direct current stimulation to the right parietal lobe. Neurosci. Lett. 479, 312– 316 10.1016/j.neulet.2010.05.087 20570713 PMC2902585 · DOI
- Bonini J. S. Cammarota M. Kerr D. S. Bevilaqua L. R. Izquierdo I. (2005). Inhibition of PKC in basolateral amygdala and posterior parietal cortex impairs consolidation of inhibitory avoidance memory. Pharmacol. Biochem. Behav. 80, 63– 67 10.1016/j.pbb.2004.10.008 15652381 · DOI · Paper page
- Bucci D. J. (2009). Posterior parietal cortex: an interface between attention and learning? Neurobiol. Learn. Mem. 91, 114– 120 10.1016/j.nlm.2008.07.004 18675370 PMC2664688 · DOI
- Buschman T. J. Miller E. K. (2007). Top-down versus bottom-up control of attention in the prefrontal and posterior parietal cortices. Science 315, 1860– 1862 17395832
- Cabeza R. Ciaramelli E. Olson I. R. Moscovitch M. (2008). The parietal cortex and episodic memory: an attentional account. Nat. Rev. Neurosci. 9, 613– 625 10.1038/nrn2459 18641668 PMC2692883 · DOI
- Cammarota M. Bevilaqua I. R. Rossato J. I. Lima R. H. Medina J. H. Izquierdo I. (2008). Parallel memory processing by the CA1 region of the dorsal hippocampus and the basolateral amygdala. Proc. Natl. Acad. Sci. U.S.A. 105, 10279– 10284 10.1073/pnas.0805284105 18647831 PMC2492498 · DOI
- Chafee M. V. Goldman-Rakic P. S. (2000). Inactivation of parietal and prefrontal cortex reveals interdependence of neural activity during memory-guided saccades. J. Neurophysiol. 83, 1550– 1566 10712479
- Chiba A. A. Kesner R. P. Jackson P. A. (2002). Two forms of spatial memory: a double dissociation between the parietal cortex and the hippocampus in the rat. Behav. Neurosci. 116, 874– 883 12369807
- Clarke J. R. Cammarota M. Gruart A. Izquierdo I. Delgado-García J. M. (2010). Plastic modifications induced by object recognition memory processing. Proc. Natl. Acad. Sci. U.S.A. 107, 2652– 2657 10.1073/pnas.0915059107 20133798 PMC2823877 · DOI · Paper page
- Compton D. M. McDaniel W. F. Dietrich K. L. (1994). Non-spatial learning following posterior parietal or hippocampal lesions. Neuroreport 5, 2189– 2192 7865774
- Constantinidis C. (2006). Posterior parietal mechanisms of visual attention. Rev. Neurosci. 17, 415– 427 17139842
- Constantinidis C. Steinmetz M. A. (1996). Neuronal activity in posterior parietal area 7a during the delay periods of a spatial memory task. J. Neurophysiol. 76, 1352– 1355 8871242
- Curtis C. E. (2006). Prefrontal and parietal contributions to spatial working memory. Neuroscience 139, 173– 180 10.1016/j.neuroscience.2005.04.070 16326021 · DOI
- Delgado-García J. M. Gruart A. (2006). Building new motor responses: eyelid conditioning revisited. Trends Neurosci. 29, 330– 338 10.1016/j.tins.2006.05.003 16713636 · DOI
- Ding S. L. Van Hoesen G. Rockland K. S. (2000). Inferior parietal lobule projections to the presubiculum and neighboring ventromedial temporal cortical areas. J. Comp. Neurol. 425, 510– 530 10975877
- Drowos D. B. Berryhill M. André J. M. Olson I. R. (2010). True memory, false memory, and subjective recollection deficits after focal parietal lobe lesions. Neuropsychology 24, 465– 475 10.1037/a0018902 20604621 PMC2917642 · DOI
- Elliott R. Dolan R. J. (1998). The neural response in short-term visual recognition memory for perceptual conjunctions. Neuroimage 7, 14– 22 10.1006/nimg.1997.0310 9500834 · DOI
- Espina-Marchant P. Pinto-Hamuy T. Bustamante D. Morales P. Robles L. Herrera-Marschitz M. (2009). Spatial cognition and memory: a reversible lesion with lidocaine into the anteromedial/posterior parietal cortex (AM/PPC) affects differently working and long-term memory on two foraging tasks. Biol. Res. 39, 601– 609 17657341
- Farovik A. Place R. J. Miller D. R. Eichenbaum H. (2011). Amygdala lesions selectively impair familiarity in recognition memory. Nat. Neurosci. 14, 1416– 1417 10.1038/nn.2919 21946327 PMC3203336 · DOI
- Flavell C. R. Barber D. J. Lee J. L. (2011). Behavioural memory reconsolidation of food and fear memories. Nat. Commun. 2, 504 10.1038/ncomms1515 22009036 PMC3516828 · DOI · Paper page
- Friedman D. de Chastelaine M. Nessler D. Malcolm B. (2010). Changes in familiarity and recollection across the lifespan: an ERP perspective. Brain Res. 1310, 124– 141 10.1016/j.brainres.2009.11.016 19914220 PMC2812671 · DOI
- Friedman-Hill S. R. Robertson L. C. Desimone R. Ungerleider L. G. (2003). Posterior parietal cortex and the filtering of distractors. Proc. Natl. Acad. Sci. U.S.A. 100, 4263– 4268 10.1073/pnas.0730772100 12646699 PMC153081 · DOI
- Gold P. E. (1986). The use of avoidance training in studied of modulation of memory storage. Behav. Neural Biol. 46, 87– 98 3015121
- Goldman-Rakic P. S. (1991). “Prefrontal cortical dysfunction in schizophrenia: the relevance of working memory,” in Psychopathology and the Brain ed Carroll B. J. Barrett J. E. (New York, NY: Raven Press), 97– 112
- Goodrich-Hunsaker N. J. Hunsaker M. R. Kesner R. P. (2005). Dissociating the role of the parietal cortex and dorsal hippocampus for spatial information processing. Behav. Neurosci. 119, 1307– 1315 10.1037/0735-7044.119.5.1307 16300437 · DOI
- Haramati S. Soroker N. Dudai Y. Levy D. A. (2008). The posterior parietal cortex in recognition memory: a neuropsychological study. Neuropsychologia 46, 1756– 1766 10.1016/j.neuropsychologia.2007.11.015 18178228 · DOI
- Holmes M. C. Carter R. N. Noble J. Chitnis S. Dutia A. Paterson J. M. Mullins J. J. Seckl J. R. Yau J. L. (2010). 11beta-hydroxysteroid dehydrogenase type 1 expression is increased in the aged mouse hippocampus and parietal cortex and causes memory impairments. J. Neurosci. 30, 6916– 6920 10.1523/JNEUROSCI.0731-10.2010 20484633 PMC2885438 · DOI
- Ingles J. L. Beninger R. J. Jhamandas K. Boegman R. J. (1993). Scopolamine injected into the rat amygdala impairs working memory in the double Y-maze. Brain Res. Bull. 32, 339– 344 10.1016/0361-9230(93)90197-J 8221123 · DOI
- Izquierdo I. Bevilaqua L. R. M. Rossato J. I. Bonini J. S. Medina J. H. Cammarota M. (2006). Different molecular cascades in different sites of the brain control consolidation. Trends Neurosci. 29, 496– 505 10.1016/j.tins.2006.07.005 16872686 · DOI
- Izquierdo I. Izquierdo L. A. Barros D. M. Mello e Souza T. de Souza M. M. Quevedo J. Rodrigues C. Kauer Sant'Anna M. Madruga M. Medina J. H. (1998). Differential involvement of cortical receptor mechanisms in working, short- and long-term memory. Behav. Pharmacol. 9, 421– 427 9832927
- Izquierdo I. Medina J. H. (1997). Memory formation: the sequence of biochemical events in the hippocampus and its connection to activity in other brain structures. Neurobiol. Learn. Mem. 68, 285– 316 10.1006/nlme.1997.3799 9398590 · DOI · Paper page
- Izquierdo I. Quillfeldt J. A. Zanatta M. S. Quevedo J. Schaeffer E. Schmitz P. K. Medina J. H. (1997). Sequential involvement of hippocampus and amygdala, entorhinal cortex and parietal cortex in the formation and expression of memory for inhibitory avoidance in rats. Eur. J. Neurosci. 9, 786– 793 9153585
- Izquierdo L. A. Barros D. M. da Costa J. C. Furini C. Zinn C. Cammarota M. Bevilaqua L. R. Izquierdo I. (2007). A link between role of two prefrontal areas in immediate memory and in long-term memory consolidation. Neurobiol. Learn. Mem. 88, 160– 188 10.1016/j.nlm.2007.04.014 17562373 · DOI
- Jiménez-Díaz L. Sancho-Bielsa F. Gruart A. Lopéz-García C. Delgado-García J. M. (2006). Evolution of cerebral cortex involvement in the acquisition of associative learning. Behav. Neurosci. 120, 1043– 1056 10.1037/0735-7044.120.5.1043 17014256 · DOI
- Jerde T. A. Childs S. K. Handy S. T. Nagode J. C. Pardo J. V. (2011). Dissociable systems of working memory for rhythm and melody. Neuroimage 57, 1572– 1579 10.1016/j.neuroimage.2011.05.061 21645625 · DOI
- Joelving F. C. Compte A. Constantinidis C. (2007). Temporal properties of posterior parietal neuron discharges during working memory and passive viewing. J. Neurophysiol. 97, 2254– 2266 10.1152/jn.00977.2006 17202244 · DOI
- Kang S. S. Sponheim S. R. Chafee M. V. MacDonald A. W. 3rd. (2011). Disrupted functional connectivity for controlled visual processing as a basis for impaired spatial working memory in schizophrenia. Neuropsychologia 49, 2836– 2847 10.1016/j.neuropsychologia.2011.06.009 21703287 PMC3156358 · DOI
- Kart-Teke E. De Souza Silva M. A. Huston J. P. Dere E. (2006). Wistar rats show episodic-like memory for unique experiences. Neurobiol. Learn. Mem. 85, 173– 182 10.1016/j.nlm.2005.10.002 16290193 · DOI · Paper page
- Keene C. S. Bucci D. J. (2008). Contributions of the retrosplenial and posterior parietal cortices to cue-specific and contextual fear conditioning. Behav. Neurosci. 122, 89– 97 10.1037/0735-7044.122.1.89 18298252 · DOI
- Kesner R. P. (2009). The posterior parietal cortex and long-term memory representation of spatial information. Learn. Mem. 91, 197– 206 10.1016/j.nlm.2008.09.004 18835456 PMC2675271 · DOI
- Lepage M. Pelletier M. Achim A. Montoya A. Menear M. Lal S. (2010). Parietal cortex and episodic memory retrieval in schizophrenia. Psychiatry Res. 182, 191– 199 10.1016/j.pscychresns.2010.03.002 20488673 · DOI
- Luft T. Pereira G. S. Cammarota M. Izquierdo I. (2004). Different time course for the memory facilitating effect of bicuculline in hippocampus, entorhinal cortex, and posterior parietal cortex of rats. Neurobiol. Learn. Mem. 82, 52– 56 10.1016/j.nlm.2004.03.002 15183170 · DOI
- McCormick C. Moscovitch M. Protzner A. B. Huber C. G. McAndrews M. P. (2010). Hippocampal-neocortical networks differ during encoding and retrieval of relational memory: functional and effective connectivity analyses. Neuropsychologia 48, 3272– 3281 10.1016/j.neuropsychologia.2010.07.010 20637787 · DOI
- McGaugh J. L. (1966). Time-dependent processes in memory storage. Science 153, 1351– 1358 10.1126/science.153.3742.1351 5917768 · DOI · Paper page
- McGaugh J. L. (2000). Memory: a century of consolidation. Science 287, 248– 251 10634773
- McVea D. A. Pearson K. G. (2009). Object avoidance during locomotion. Adv. Exp. Med. Biol. 629, 293– 315 10.1007/978-0-387-77064-2_15 19227506 · DOI
- McVea D. A. Taylor A. J. Pearson K. G. (2009). Long-lasting working memories of obstacles established by foreleg stepping in walking cats require area 5 of the posterior parietal cortex. J. Neurosci. 29, 9396– 9404 10.1523/JNEUROSCI.0746-09.2009 19625530 PMC6665557 · DOI
- Myskiw J. C. Fiorenza N. G. Izquierdo L. A. Izquierdo I. (2010). Molecular mechanisms in hippocampus and basolateral amygdala but not in parietal or cingulate cortex are involved in extinction of one-trial avoidance learning. Neurobiol. Learn. Mem. 94, 285– 291 10.1016/j.nlm.2010.06.007 20601026 · DOI
- Nagappan G. Lu B. (2005). Activity-dependent modulation of the BDNF receptor TrkB: mechanisms and implications. Trends Neurosci. 28, 464– 471 10.1016/j.tins.2005.07.003 16040136 · DOI
- Okaichi H. Hojo M. Okaichi Y. (2006). Effects of post-training lesions in the hippocampus and the parietal cortex on idiothetic information processing in the rat. Rev. Neurosci. 17, 135– 146 16703947
- Olson I. R. Berryhill M. (2009). Some surprising findings on the involvement of the parietal lobe in human memory. Neurobiol. Learn. Mem. 91, 155– 165 10.1016/j.nlm.2008.09.006 18848635 PMC2898273 · DOI
- Otsuka Y. Osaka N. Osaka M. (2008). Functional asymmetry of superior parietal lobule for working memory in the elderly. Neuroreport 19, 1355– 1359 10.1097/WNR.0b013e32830e000f 18766010 · DOI
- Pinto-Hamuy T. Montero V. M. Torrealba F. (2004). Neurotoxic lesion of anteromedial/posterior parietal cortex disrupts spatial maze memory in blind rats. Behav. Brain Res. 153, 465– 470 10.1016/j.bbr.2004.01.003 15265644 · DOI
- Quintana J. Fuster J. M. (1999). From perception to action: temporal integrative functions of prefrontal and parietal neurons. Cereb. Cortex 9, 213– 221 10.1093/cercor/9.3.213 10355901 · DOI
- Rawley J. B. Constantinidis C. (2009). Neural correlates of learning and working memory in the primate posterior parietal cortex. Neurobiol. Learn. Mem. 91, 129– 138 10.1016/j.nlm.2008.12.006 19116173 PMC2663957 · DOI
- Reep R. L. Corwin J. V. (2009). Posterior parietal cortex as part of a neural network for directed attention in rats. Neurobiol. Learn. Mem. 91, 104– 113 10.1016/j.nlm.2008.08.010 18824116 · DOI
- Richmond L. L. Morrison A. B. Chein J. M. Olson I. R. (2011). Working memory training and transfer in older adults. Psychol. Aging 26, 813– 822 10.1037/a0023631 21707176 · DOI
- Rogers J. L. Kesner R. P. (2007). Hippocampal-parietal cortex interactions: evidence from a disconnection study in the rat. Behav. Brain Res. 179, 19– 27 10.1016/j.bbr.2007.01.019 17336404 PMC2095781 · DOI
- Rossato J. I. Bonini J. S. Cammarota M. Medina J. H. Izquierdo I. (2004). Retrograde amnesia induced by drugs acting on different molecular systems. Behav. Neurosci. 118, 563– 568 10.1037/0735-7044.118.3.563 15174933 · DOI
- Rugg M. D. Curran T. (2007). Event-related potentials and recognition memory. Trends Cogn. Sci. 11, 251– 257 10.1016/j.tics.2007.04.004 17481940 · DOI
- Schoo L. A. van Zandvoort M. J. Biessels G. J. Kappelle L. J. Postma A. de Haan E. H. (2011). The posterior parietal paradox: why do functional magnetic resonance imaging and lesion studies on episodic memory produce conflicting results? J. Neuropsychol. 5, 15– 38 10.1348/174866410X504059 21366885 · DOI
- Schröder N. de-Paris F. Roesler R. Medina J. H. Souza D. O. Izquierdo I. (2000). Effect of inhibtory avoidance training on 3H-glutamate binding in the hippocampus and parietal cortex of rats. Braz. J. Med. Biol. Res. 33, 229– 232 10657064
- Schwabe L. Wolf O. T. (2011). Stress-induced modulation of instrumental behavior: from goal-directed to habitual control of action. Behav. Brain Res. 219, 321– 328 10.1016/j.bbr.2010.12.038 21219935 · DOI
- Sohn M. H. Goode A. Stenger V. A. Jung K. J. Carter C. S. Anderson J. R. (2005). An information-processing model of three cortical regions: evidence in episodic memory retrieval. Neuroimage 25, 21– 33 10.1016/j.neuroimage.2004.11.001 15734340 · DOI
- Szapiro G. Izquierdo L. A. Alonso M. Barros D. Paratcha G. Ardenghi P. Pereira P. Medina J. H. Izquierdo I. (2000). Participation of hippocampal metabotropic glutamate receptors, protein kinase A and mitogen-activated protein kinases in memory retrieval. Neuroscience 99, 1– 5 10.1016/S0306-4522(00)00236-0 10924946 · DOI
- Weiss A. P. Ellis C. B. Roffman J. L. Stufflebeam S. Hamalainen M. S. Duff M. Goff D. C. Schacter D. L. (2009). Aberrant frontoparietal function during recognition memory in schizophrenia: a multimodal neuroimaging investigation. J. Neurosci. 29, 11347– 11359 10.1523/JNEUROSCI.0617-09.2009 19741141 PMC2768128 · DOI
- Weymar M. Löw A. Hamm A. O. (2011). Emotional memories are resilient to time: evidence from the parietal ERP old/new effect. Hum. Brain Mapp. 32, 632– 640 10.1002/hbm.21051 21391253 PMC6870483 · DOI
- Weymar M. Löw A. Modess C. Engel G. Gründling M. Petersmann A. Siegmund W. Hamm A. O. (2010). Propranolol selectively blocks the enhanced parietal old/new effect during long-term recollection of unpleasant pictures: a high density ERP study. Neuroimage 49, 2800– 2806 10.1016/j.neuroimage.2009.10.025 19837180 · DOI
- Whitlock J. R. Heynen A. J. Shuler M. G. Bear M. F. (2006). Learning induces long-term potentiation in the hippocampus. Science 313, 1093– 1097 10.1126/science.1128134 16931756 · DOI · Paper page
- Whitlock J. R. Sutherland R. J. Witter M. P. Moser M. B. Moser E. I. (2008). Navigating from hippocampus to parietal cortex. Proc. Natl. Acad. Sci. U.S.A. 105, 14755– 14762 10.1073/pnas.0804216105 18812502 PMC2567440 · DOI · Paper page
- Winters B. D. Reid J. M. (2010). A distributed cortical representation underlies crossmodal object recognition in rats. J. Neurosci. 30, 6253– 6261 10.1523/JNEUROSCI.6073-09.2010 20445051 PMC6632708 · DOI
- Zanatta M. S. Schaeffer E. Schmitz P. K. Medina J. H. Quevedo J. Quillfeldt J. A. Izquierdo I. (1996). Sequential involvement of NMDA-dependent mechanisms in hippocampus, amygdala, entorhinal cortex and parietal cortex in memory processing. Behav. Pharmacol. 7, 341– 345 11224427
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“Posterior parietal cortex activations have consistently been observed during episodic retrieval tasks (Hutchinson et al., 2009; Myskiw and Izquierdo, 2012).”
Background
- Authors
- Myskiw, J. C., & Izquierdo, I.
- Affiliations
- Instituto do Cérebro (BR)
- Corresponding author
- Izquierdo, Iván
- ORCID
- Izquierdo, Iván
- Venue
- Frontiers in Integrative Neuroscience
- Publisher
- Frontiers Media SA
- Published
- 2012
- Volume
- 6
- Pages
- 8-8
- ISSN
- 1662-5145 (ISSN-L)
- PMC
- PMC3287050
- OpenAlex
- W2152972730
- Cited by
- 24
- References
- 2
- Citations by year
- 2026: 2 · 2025: 1 · 2024: 1 · 2023: 2 · 2022: 3 · 2021: 2 · 2020: 2 · 2019: 2 · 2017: 2 · 2016: 3 · 2015: 2 · 2014: 2
- FWCI
- 0.66
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by-nc
- Locations
- Frontiers in Integrative Neuroscience (publishedVersion, cc-by-nc)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas) (publishedVersion, other-oa)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Cognitive Functions and Memory
- Keywords
- posterior parietal cortex, long-term memory, episodic memory, memory consolidation, memory retrieval, working memory, neurotransmitters, rodent models, lesion studies, hippocampus, basolateral amygdala, spatial perception
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