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Kv4.2 mediates histamine modulation of preoptic neuron activity and body temperature.

Abstract

Histamine regulates arousal, circadian rhythms, and thermoregulation. Activation of H3 histamine receptors expressed by preoptic GABAergic neurons results in a decrease of their firing rate and hyperthermia. Here we report that an increase in the A-type K⁺ current in preoptic GABAergic neurons in response to activation of H3 histamine receptors results in decreased firing rate and hyperthermia in mice. The Kv4.2 subunit is required for these actions in spite of the fact that Kv4.2⁻/⁻ preoptic GABAergic neurons display A-type currents and firing characteristics similar to those of wild-type neurons. This electrical remodeling is achieved by robust upregulation of the expression of the Kv4.1 subunit and of a delayed rectifier current. Dynamic clamp experiments indicate that enhancement of the A-type current by a similar amount to that induced by histamine is sufficient to mimic its robust effect on firing rates. These data indicate a central role played by the Kv4.2 subunit in histamine regulation of body temperature and its interaction with pERK1/2 downstream of the H3 receptor. We also reveal that this pathway provides a mechanism for selective modulation of body temperature at the beginning of the active phase of the circadian cycle.

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  • Authors

    Sethi J, Sanchez-Alavez M, Tabarean IV

    Institution

    The Department of Molecular and Integrative Neurosciences, The Scripps Research Institute, La Jolla, California, United States of America.

    Source

    PloS one 6:12 2011 pg e29134

    MeSH

    Action Potentials
    Animals
    Body Temperature
    Circadian Rhythm
    GABAergic Neurons
    Histamine
    Histamine Agonists
    Injections
    Ion Channel Gating
    Kinetics
    Male
    Mice
    Mice, Inbred C57BL
    Motor Activity
    Neurons
    Patch-Clamp Techniques
    Preoptic Area
    Protein Subunits
    Receptors, Histamine H3
    Shal Potassium Channels
    Spider Venoms
    Up-Regulation

    Pub Type(s)

    Journal Article
    Research Support, N.I.H., Extramural

    Language

    eng

    PubMed ID

    22220205