Literature DB >> 17272655

Memory is not extinguished along with CS presentation but within a few seconds after CS-offset.

Luis María Pérez-Cuesta1, Yanil Hepp, María Eugenia Pedreira, Héctor Maldonado.   

Abstract

Prior work with the crab's contextual memory model showed that CS-US conditioned animals undergoing an unreinforced CS presentation would either reconsolidate or extinguish the CS-US memory, depending on the length of the reexposure to the CS. Either memory process is only triggered once the CS is terminated. Based on these results, the following questions are raised. First, when is extinction memory acquired, if not along extinction training, and how long does it take? Second, can acquisition and consolidation of extinction memory be pharmacologically dissected? Here we address these questions performing three series of experiments: a first one aimed to study systematically the relationship between extinction and increasing periods of unreinforced CS presentations, a second one to determine the time boundaries of the extinction memory acquisition, and the third one to assay the requirement for protein synthesis and NMDA-like receptors of acquisition and consolidation of extinction memory. Our results confirm that it is CS-offset and not the mere retrieval (CS-onset) that triggers acquisition of extinction memory and that it is completed in less than 45 sec after CS-offset. In addition, protein synthesis is required for consolidation but not for acquisition of this memory and, conversely, NMDA-like receptor activity is required for its acquisition but not for its consolidation. Finally, we offer an interpretative scheme of our results and we discuss to what extent it could apply to multitrial extinction.

Entities:  

Year:  2007        PMID: 17272655      PMCID: PMC1838540          DOI: 10.1101/lm.413507

Source DB:  PubMed          Journal:  Learn Mem        ISSN: 1072-0502            Impact factor:   2.460


  29 in total

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2.  Delayed recall of fear extinction in rats with lesions of ventral medial prefrontal cortex.

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4.  The role of NMDA glutamate receptors, PKA, MAPK, and CAMKII in the hippocampus in extinction of conditioned fear.

Authors:  German Szapiro; Monica R M Vianna; James L McGaugh; Jorge H Medina; Ivan Izquierdo
Journal:  Hippocampus       Date:  2003       Impact factor: 3.899

5.  An arthropod NMDA receptor.

Authors:  C Pfeiffer-Linn; R M Glantz
Journal:  Synapse       Date:  1991-09       Impact factor: 2.562

6.  Reactivation and reconsolidation of long-term memory in the crab Chasmagnathus: protein synthesis requirement and mediation by NMDA-type glutamatergic receptors.

Authors:  María Eugenia Pedreira; Luis María Pérez-Cuesta; Héctor Maldonado
Journal:  J Neurosci       Date:  2002-09-15       Impact factor: 6.167

7.  Adrenergic transmission facilitates extinction of conditional fear in mice.

Authors:  Christopher K Cain; Ashley M Blouin; Mark Barad
Journal:  Learn Mem       Date:  2004 Mar-Apr       Impact factor: 2.460

8.  The similarities and diversities of signal pathways leading to consolidation of conditioning and consolidation of extinction of fear memory.

Authors:  Chih-Hung Lin; Shiu-Hwa Yeh; Hsin-Yi Lu; Po-Wu Gean
Journal:  J Neurosci       Date:  2003-09-10       Impact factor: 6.167

9.  Consolidation of fear extinction requires protein synthesis in the medial prefrontal cortex.

Authors:  Edwin Santini; Hong Ge; Keqin Ren; Sandra Peña de Ortiz; Gregory J Quirk
Journal:  J Neurosci       Date:  2004-06-23       Impact factor: 6.167

10.  Reconsolidation of a long-term memory in Lymnaea requires new protein and RNA synthesis and the soma of right pedal dorsal 1.

Authors:  Susan Sangha; Andi Scheibenstock; Ken Lukowiak
Journal:  J Neurosci       Date:  2003-09-03       Impact factor: 6.167

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  8 in total

1.  Expanding the intertrial interval during extinction: response cessation and recovery.

Authors:  Alyssa J Orinstein; Gonzalo P Urcelay; Ralph R Miller
Journal:  Behav Ther       Date:  2009-06-01

2.  Context-dependent memory traces in the crab's mushroom bodies: Functional support for a common origin of high-order memory centers.

Authors:  Francisco Javier Maza; Julieta Sztarker; Avishag Shkedy; Valeria Natacha Peszano; Fernando Federico Locatelli; Alejandro Delorenzi
Journal:  Proc Natl Acad Sci U S A       Date:  2016-11-16       Impact factor: 11.205

3.  Shifting from fear to safety through deconditioning-update.

Authors:  Bruno Popik; Felippe Espinelli Amorim; Olavo B Amaral; Lucas De Oliveira Alvares
Journal:  Elife       Date:  2020-01-30       Impact factor: 8.140

4.  Extinction learning, which consists of the inhibition of retrieval, can be learned without retrieval.

Authors:  Jociane de Carvalho Myskiw; Cristiane Regina Guerino Furini; Bianca Schmidt; Flávia Ferreira; Ivan Izquierdo
Journal:  Proc Natl Acad Sci U S A       Date:  2014-12-30       Impact factor: 11.205

Review 5.  Serotonergic mechanisms in addiction-related memories.

Authors:  Bríd A Nic Dhonnchadha; Kathryn A Cunningham
Journal:  Behav Brain Res       Date:  2008-07-01       Impact factor: 3.332

6.  Protein degradation by ubiquitin-proteasome system in formation and labilization of contextual conditioning memory.

Authors:  María Sol Fustiñana; Verónica de la Fuente; Noel Federman; Ramiro Freudenthal; Arturo Romano
Journal:  Learn Mem       Date:  2014-08-18       Impact factor: 2.460

7.  Surface expression of NMDA receptor changes during memory consolidation in the crab Neohelice granulata.

Authors:  Yanil Hepp; Angeles Salles; Martin Carbo-Tano; Maria Eugenia Pedreira; Ramiro Freudenthal
Journal:  Learn Mem       Date:  2016-07-15       Impact factor: 2.460

8.  Memory extinction entails the inhibition of the transcription factor NF-kappaB.

Authors:  Emiliano Merlo; Arturo Romano
Journal:  PLoS One       Date:  2008-11-10       Impact factor: 3.240

  8 in total

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