Literature DB >> 11876782

Physiological properties of central amygdala neurons: species differences.

Eric C Dumont1, Marzia Martina, Rachel D Samson, Guy Drolet, Denis Paré.   

Abstract

The connections of limbic structures are remarkably constant across species. However, different species express fear in distinct ways. Because the central amygdaloid nucleus is considered an important mediator of fear responses, we compared the physiological properties of central amygdala neurons in guinea pigs, rats and cats using whole-cell recordings in coronal slices in vitro. In guinea pigs, most central medial and lateral neurons displayed an outward rectification that delayed firing onset in response to depolarizing current pulses (hence the designation late-firing neurons). Late-firing neurons were also prevalent in the lateral sector of the cat central nucleus. In contrast, late-firing neurons were rare in the rat central nucleus and the cat central medial nucleus. There, most neurons generated Ni2+-sensitive low-threshold bursts of Na+ spikes and/or displayed pronounced inward rectification in the hyperpolarizing direction. Species differences in passive properties were also observed, but they were mainly related to the relative prevalence of late-firing cells. Indeed, late-firing cells had a significantly lower input resistance and more negative membrane potential than other types of central neurons. Thus, there are marked species differences in the physiological properties of central neurons. Because the synaptic responsiveness of neurons is constrained by their physiological properties, our findings raise the possibility that the contrasting behavioural responsiveness observed across species is partly dependent on the species-specific physiological properties of central neurons.

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Year:  2002        PMID: 11876782     DOI: 10.1046/j.0953-816x.2001.01879.x

Source DB:  PubMed          Journal:  Eur J Neurosci        ISSN: 0953-816X            Impact factor:   3.386


  37 in total

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Review 2.  Plastic synaptic networks of the amygdala for the acquisition, expression, and extinction of conditioned fear.

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3.  Optogenetic study of the projections from the bed nucleus of the stria terminalis to the central amygdala.

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4.  Fear signaling in the prelimbic-amygdala circuit: a computational modeling and recording study.

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5.  Impact of infralimbic inputs on intercalated amygdala neurons: a biophysical modeling study.

Authors:  Guoshi Li; Taiju Amano; Denis Pare; Satish S Nair
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Review 6.  The amygdala and medial prefrontal cortex: partners in the fear circuit.

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Journal:  J Physiol       Date:  2013-02-18       Impact factor: 5.182

7.  Novel subunit-specific tonic GABA currents and differential effects of ethanol in the central amygdala of CRF receptor-1 reporter mice.

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Journal:  J Neurosci       Date:  2013-02-20       Impact factor: 6.167

8.  Ultrastructural relationship between N-methyl-D-aspartate-NR1 receptor subunit and mu-opioid receptor in the mouse central nucleus of the amygdala.

Authors:  M J Glass; L Vanyo; L Quimson; V M Pickel
Journal:  Neuroscience       Date:  2009-07-14       Impact factor: 3.590

9.  The central amygdala to periaqueductal gray pathway comprises intrinsically distinct neurons differentially affected in a model of inflammatory pain.

Authors:  Jun-Nan Li; Patrick L Sheets
Journal:  J Physiol       Date:  2018-11-02       Impact factor: 5.182

10.  Amygdala projections to central amygdaloid nucleus subdivisions and transition zones in the primate.

Authors:  J L Fudge; T Tucker
Journal:  Neuroscience       Date:  2009-03-17       Impact factor: 3.590

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