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Cellular effects of swim stress in the dorsal raphe nucleus.

Cellular effects of swim stress in the dorsal raphe nucleus. Research Abstract Details 

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  • Cellular effects of swim stress in the dorsal raphe nucleus. Abstract Text:

    lynn g kirbyLynn G Kirby,yu-zhen panYu-Zhen Pan,emily freeman-danielsEmily Freeman-Daniels,shobha raniShobha Rani,john d nunanJohn D Nunan,adaure akanwaAdaure Akanwa,sheryl g beckSheryl G Beck,lynn g kirbyLynn G Kirby,yu-zhen panYu-Zhen Pan,emily freeman-danielsEmily Freeman-Daniels,shobha raniShobha Rani,john d nunanJohn D Nunan,adaure akanwaAdaure Akanwa,sheryl g beckSheryl G Beck,

    Swim stress regulates forebrain 5-hydroxytryptamine (5-HT) release in a complex manner and its effects are initiated in the serotonergic dorsal raphe nucleus (DRN). The purpose of this study was to examine the effects of swim stress on the physiology of DRN neurons in conjunction with 5-HT immunohistochemistry. Basic membrane properties, 5-HT(1A) and 5-HT(1B) receptor-mediated responses and glutamatergic excitatory postsynaptic currents (EPSCs) were measured using whole-cell patch clamp techniques. Rats were forced to swim for 15min and 24h later DRN brain slices were prepared for electrophysiology. Swim stress altered the resting membrane potential, input resistance and action potential duration of DRN neurons in a neurochemical-specific manner. Swim stress selectively elevated glutamate EPSC frequency in 5-HT DRN neurons. Swim stress non-selectively reduced EPSC amplitude in all DRN cells. Swim stress elevated the 5-HT(1B) receptor-mediated inhibition of glutamatergic synaptic activity that selectively targeted 5-HT cells. Non-5-HT DRN neurons appeared to be particularly responsive to the effects of a milder handling stress. Handling elevated EPSC frequency, reduced EPSC decay time and enhanced a 5-HT(1B) receptor-mediated inhibition of mEPSC frequency selectively in non-5-HT DRN cells. These results indicate that swim stress has both direct, i.e., changes in membrane characteristics, and indirect effects, i.e., via glutamatergic afferents, on DRN neurons. These results also indicate that there are distinct local glutamatergic afferents to neurochemically specific populations of DRN neurons, and furthermore that these distinct afferents are differentially regulated by swim stress. These cellular changes may contribute to the complex effects of swim stress on 5-HT neurotransmission and/or the behavioral changes underlying the forced swimming test model of depression.

    Cellular effects of swim stress in the dorsal raphe nucleus. Publishing Authors By Initials

    lg kirbyLG Kirby,yz panYZ Pan,e freeman-danielsE Freeman-Daniels,s raniS Rani,jd nunanJD Nunan,a akanwaA Akanwa,sg beckSG Beck,lg kirbyLG Kirby,yz panYZ Pan,e freeman-danielsE Freeman-Daniels,s raniS Rani,jd nunanJD Nunan,a akanwaA Akanwa,sg beckSG Beck,

    For similar synaptic transmission research abstracts see: synaptic transmission research

    PUBMED ID PMID:

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    Cellular effects of swim stress in the dorsal raphe nucleus. Journal Published:

    PUBLICATION TYPE: Research Support, U.S. Gov't,

    Journal: Psychoneuroendocrinology

    VOLUME: 32

    Page Numbers: 712-23

    Journal Abbreviation: Psychoneuroendocrinology

    ISSN: 0306-4530

    DAY: 28

    MONTH: 06

    YEAR: 2007

    Cellular effects of swim stress in the dorsal raphe nucleus. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 7612148

    Cellular effects of swim stress in the dorsal raphe nucleus. Keywords Mesh Terms:

    KEYWORDS: Synaptic Transmission

    MESH TERMS: physiology

    Chemical & Substance for Abstract: Cellular effects of swim stress in the dorsal raphe nucleus. Information

    Substance Name: Serotonin

    Registry Number: 50-67-9

    Grant and Affiliation Information for Cellular effects of swim stress in the dorsal raphe nucleus.

    AFFILIATION: Department of Anatomy and Cell Biology, Temple University School of Medicine, Philadelphia, PA 19140, USA. lkirby@temple.edu

    Country: England

    England Research PublicationEngland Research Publication

    AGENCY: United States NIMH

    GRANT: MH75047

    ACRONYM: MH

    MEDLINETA: Psychoneuroendocrinology

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