Literature DB >> 11473133

Mitogen-activated protein kinase cascade in the basolateral nucleus of amygdala is involved in extinction of fear-potentiated startle.

K T Lu1, D L Walker, M Davis.   

Abstract

Previous results indicate that intra-amygdala infusions of NMDA receptor antagonists block the extinction of conditioned fear. Mitogen-activated protein kinase (MAPK) can be activated by NMDA receptor stimulation and is involved in excitatory fear conditioning. Here, we evaluate the role of MAPK within the basolateral amygdala in the extinction of conditioned fear. Rats received 10 light-shock pairings. After 24 hr, fear was assessed by eliciting the acoustic startle reflex in the presence of the conditioned stimulus (CS) (CS-noise trials) and also in its absence (noise-alone trials). Rats subsequently received an intra-amygdala or intrahippocampal infusion of either 20% DMSO or the MAPK inhibitor PD98059 (500 ng/side) followed 10 min later by 30 presentations of the light CS without shock (extinction training). After 24 hr, they were again tested for fear-potentiated startle. PD98059 infusions into the basolateral amygdala but not the hippocampus significantly reduced extinction, which was otherwise evident in DMSO-infused rats. Control experiments indicated that the effect of intra-amygdala PD98059 could not be attributed to lasting damage to the amygdala or to state dependency. These results suggest that a MAPK-dependent signaling cascade within or very near the basolateral amygdala plays an important role in the extinction of conditioned fear.

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Year:  2001        PMID: 11473133      PMCID: PMC6763147     

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  60 in total

1.  L-type voltage-gated calcium channels are required for extinction, but not for acquisition or expression, of conditional fear in mice.

Authors:  Chris K Cain; Ashley M Blouin; Mark Barad
Journal:  J Neurosci       Date:  2002-10-15       Impact factor: 6.167

Review 2.  Molecular specificity of multiple hippocampal processes governing fear extinction.

Authors:  Jelena Radulovic; Natalie C Tronson
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3.  Inhibition of mRNA and protein synthesis in the CA1 region of the dorsal hippocampus blocks reinstallment of an extinguished conditioned fear response.

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Journal:  J Neurosci       Date:  2003-02-01       Impact factor: 6.167

Review 4.  Molecular mechanisms of memory retrieval.

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Journal:  Neurochem Res       Date:  2002-11       Impact factor: 3.996

5.  Context-dependent neuronal activity in the lateral amygdala represents fear memories after extinction.

Authors:  Jennifer A Hobin; Ki A Goosens; Stephen Maren
Journal:  J Neurosci       Date:  2003-09-10       Impact factor: 6.167

Review 6.  Neural and cellular mechanisms of fear and extinction memory formation.

Authors:  Caitlin A Orsini; Stephen Maren
Journal:  Neurosci Biobehav Rev       Date:  2012-01-02       Impact factor: 8.989

Review 7.  Plastic synaptic networks of the amygdala for the acquisition, expression, and extinction of conditioned fear.

Authors:  Hans-Christian Pape; Denis Pare
Journal:  Physiol Rev       Date:  2010-04       Impact factor: 37.312

8.  Hippocampal Mek/Erk signaling mediates extinction of contextual freezing behavior.

Authors:  Andre Fischer; Marko Radulovic; Christina Schrick; Farahnaz Sananbenesi; Jasminka Godovac-Zimmermann; Jelena Radulovic
Journal:  Neurobiol Learn Mem       Date:  2006-09-18       Impact factor: 2.877

9.  Genetic disruptions of Drosophila Pavlovian learning leave extinction learning intact.

Authors:  H Qin; J Dubnau
Journal:  Genes Brain Behav       Date:  2009-10-28       Impact factor: 3.449

10.  Neuropeptide S-mediated control of fear expression and extinction: role of intercalated GABAergic neurons in the amygdala.

Authors:  Kay Jüngling; Thomas Seidenbecher; Ludmila Sosulina; Jörg Lesting; Susan Sangha; Stewart D Clark; Naoe Okamura; Dee M Duangdao; Yan-Ling Xu; Rainer K Reinscheid; Hans-Christian Pape
Journal:  Neuron       Date:  2008-07-31       Impact factor: 17.173

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