Literature DB >> 14704220

Acute stress-induced changes in hippocampal/prefrontal circuits in rats: effects of antidepressants.

Cyril Rocher1, Michael Spedding, Carmen Munoz, Thérèse M Jay.   

Abstract

Acute stress inhibits long-term potentiation (LTP) at synapses from the hippocampus to prefrontal cortex in the rat, a model of the dysfunction in the anterior cingulate/orbitofrontal cortices which has been observed in human depression. We demonstrate that the antidepressants tianeptine and, to a lesser extent, fluoxetine, are able to reverse the impairment in LTP, a measure of frontal synaptic plasticity, caused by stress on an elevated platform. LTP was induced by stimulation of hippocampal outflow. Beneficial effects on neuronal plasticity, defined as a reversal of the effects of stress in this paradigm, can be considered as a new animal model for the impact of stress on hippocampal/frontal circuits, a key target in psychiatric diseases.

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Year:  2004        PMID: 14704220     DOI: 10.1093/cercor/bhg122

Source DB:  PubMed          Journal:  Cereb Cortex        ISSN: 1047-3211            Impact factor:   5.357


  92 in total

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Review 4.  Common efficacy of psychotropic drugs in restoring stress-induced impairment of prefrontal plasticity.

Authors:  Nathalie Dupin; François Mailliet; Cyril Rocher; Karima Kessal; Michael Spedding; Therese M Jay
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Review 5.  Disruption of cortical-limbic interaction as a substrate for comorbidity.

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Review 7.  Towards a glutamate hypothesis of depression: an emerging frontier of neuropsychopharmacology for mood disorders.

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8.  Fluoxetine protects hippocampal plasticity during conditioned fear stress and prevents fear learning potentiation.

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Review 10.  Plasticity at hippocampal to prefrontal cortex synapses is impaired by loss of dopamine and stress: importance for psychiatric diseases.

Authors:  Thérèse M Jay; Cyril Rocher; Maïte Hotte; Laurent Naudon; Hirac Gurden; Michael Spedding
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