Literature DB >> 9880603

Reciprocal changes in the firing probability of lateral and central medial amygdala neurons.

D R Collins1, D Paré.   

Abstract

The amygdala is essential for classical fear conditioning. According to the current model of auditory fear conditioning, the lateral nucleus is the input station of the amygdala for conditioned auditory stimuli, whereas the central nucleus is the output station for conditioned fear responses. Yet, the lateral nucleus does not project to the central medial nucleus, where most brainstem projections of the amygdala originate. The available evidence suggests that the basal nuclei could transmit information from the lateral to the central medial nucleus. However, interposed between the basolateral complex and the central nucleus are clusters of GABAergic cells, the intercalated neurons, which receive inputs from the lateral and basal nuclei and contribute a massive projection to the central medial nucleus. Because it is impossible to predict the consequences of these connections, we correlated the spontaneous and auditory-evoked activity of multiple simultaneously recorded neurons of the lateral, basal, and central nuclei. The spontaneous activity of lateral and basolateral neurons was positively correlated to that of central lateral cells but negatively correlated to that of central medial neurons. In response to auditory stimuli, the firing probability of lateral and central medial neurons oscillated in phase opposition, initially being excited and inhibited, respectively. In light of previous anatomical findings, we propose that the lateral nucleus exerts two indirect actions on central medial neurons: an excitation via the basal nuclei and an inhibition via intercalated neurons.

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Year:  1999        PMID: 9880603      PMCID: PMC6782219     

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


  59 in total

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Journal:  Synapse       Date:  1990       Impact factor: 2.562

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Authors:  B H Turner; M Herkenham
Journal:  J Comp Neurol       Date:  1991-11-08       Impact factor: 3.215

3.  Synaptic responsiveness of interneurons of the cat lateral amygdaloid nucleus.

Authors:  E J Lang; D Paré
Journal:  Neuroscience       Date:  1998-04       Impact factor: 3.590

4.  Projection neurons of the lateral amygdaloid nucleus are virtually silent throughout the sleep--waking cycle.

Authors:  H Gaudreau; D Paré
Journal:  J Neurophysiol       Date:  1996-03       Impact factor: 2.714

5.  Sensitization of the startle reflex by footshock: blockade by lesions of the central nucleus of the amygdala or its efferent pathway to the brainstem.

Authors:  J M Hitchcock; C B Sananes; M Davis
Journal:  Behav Neurosci       Date:  1989-06       Impact factor: 1.912

6.  Bidirectional synaptic plasticity in the rat basolateral amygdala: characterization of an activity-dependent switch sensitive to the presynaptic metabotropic glutamate receptor antagonist 2S-alpha-ethylglutamic acid.

Authors:  H Li; S R Weiss; D M Chuang; R M Post; M A Rogawski
Journal:  J Neurosci       Date:  1998-03-01       Impact factor: 6.167

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Journal:  Brain Res       Date:  1978-10-27       Impact factor: 3.252

8.  Projections to the subcortical forebrain from anatomically defined regions of the medial geniculate body in the rat.

Authors:  J E LeDoux; D A Ruggiero; D J Reis
Journal:  J Comp Neurol       Date:  1985-12-08       Impact factor: 3.215

9.  Intrinsic connections of the rat amygdaloid complex: projections originating in the basal nucleus.

Authors:  V Savander; C G Go; J E LeDoux; A Pitkänen
Journal:  J Comp Neurol       Date:  1995-10-16       Impact factor: 3.215

10.  Immunohistochemical identification of gamma-aminobutyric acid-containing neurons in the rat basolateral amygdala.

Authors:  A J McDonald
Journal:  Neurosci Lett       Date:  1985-01-21       Impact factor: 3.046

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  17 in total

1.  An inhibitory interface gates impulse traffic between the input and output stations of the amygdala.

Authors:  S Royer; M Martina; D Paré
Journal:  J Neurosci       Date:  1999-12-01       Impact factor: 6.167

2.  Differential fear conditioning induces reciprocal changes in the sensory responses of lateral amygdala neurons to the CS(+) and CS(-).

Authors:  D R Collins; D Paré
Journal:  Learn Mem       Date:  2000 Mar-Apr       Impact factor: 2.460

3.  Lasting increases in basolateral amygdala activity after emotional arousal: implications for facilitated consolidation of emotional memories.

Authors:  Joe Guillaume Pelletier; Ekaterina Likhtik; Mohammed Filali; Denis Paré
Journal:  Learn Mem       Date:  2005 Mar-Apr       Impact factor: 2.460

4.  Distribution of serotonin transporter labeled fibers in amygdaloid subregions: implications for mood disorders.

Authors:  Howard O'Rourke; Julie L Fudge
Journal:  Biol Psychiatry       Date:  2006-01-18       Impact factor: 13.382

5.  Specificity of Primate Amygdalar Pathways to Hippocampus.

Authors:  Jingyi Wang; Helen Barbas
Journal:  J Neurosci       Date:  2018-09-24       Impact factor: 6.167

6.  Effects of repeated stress on excitatory drive of basal amygdala neurons in vivo.

Authors:  Mallika Padival; Danielle Quinette; J Amiel Rosenkranz
Journal:  Neuropsychopharmacology       Date:  2013-03-27       Impact factor: 7.853

7.  Distribution of CB1 cannabinoid receptors in the amygdala and their role in the control of GABAergic transmission.

Authors:  I Katona; E A Rancz; L Acsady; C Ledent; K Mackie; N Hajos; T F Freund
Journal:  J Neurosci       Date:  2001-12-01       Impact factor: 6.167

8.  Neuronal correlates of fear in the lateral amygdala: multiple extracellular recordings in conscious cats.

Authors:  D Paré; D R Collins
Journal:  J Neurosci       Date:  2000-04-01       Impact factor: 6.167

9.  Single-unit activity in the medial prefrontal cortex during immediate and delayed extinction of fear in rats.

Authors:  Chun-hui Chang; Joshua D Berke; Stephen Maren
Journal:  PLoS One       Date:  2010-08-05       Impact factor: 3.240

Review 10.  The extended amygdala and the dopamine system: another piece of the dopamine puzzle.

Authors:  Julie L Fudge; Ana B Emiliano
Journal:  J Neuropsychiatry Clin Neurosci       Date:  2003       Impact factor: 2.198

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