Unbound MEDLINE

Excitation of histaminergic tuberomamillary neurons by thyrotropin-releasing hormone. The Journal of neuroscience : the official journal of the Society for Neuroscience [J Neurosci] Journal article

 
TitleExcitation of histaminergic tuberomamillary neurons by thyrotropin-releasing hormone.
Author(s)Parmentier R, Kolbaev S, Klyuch BP, Vandael D, Lin JS, Selbach O, Haas HL, Sergeeva OA 
InstitutionDepartment of Neurophysiology, Heinrich Heine University, Duesseldorf, Germany.
SourceJ Neurosci 2009 Apr 8; 29(14):4471-83.
MeSHAction Potentials
Animals
Calcium Channels
Cations, Divalent
Histamine
Hypothalamic Area, Lateral
Inhibitory Postsynaptic Potentials
Male
Mice
Mice, Knockout
Neurons
Rats
Rats, Wistar
Receptors, Thyrotropin-Releasing Hormone
Sleep Stages
Sodium Channels
Thyrotropin-Releasing Hormone
AbstractThe histaminergic tuberomamillary nucleus (TMN) controls arousal and attention, and the firing of TMN neurons is state-dependent, active during waking, silent during sleep. Thyrotropin-releasing hormone (TRH) promotes arousal and combats sleepiness associated with narcolepsy. Single-cell reverse-transcription-PCR demonstrated variable expression of the two known TRH receptors in the majority of TMN neurons. TRH increased the firing rate of most (ca 70%) TMN neurons. This excitation was abolished by the TRH receptor antagonist chlordiazepoxide (CDZ; 50 mum). In the presence of tetrodotoxin (TTX), TRH depolarized TMN neurons without obvious change of their input resistance. This effect reversed at the potential typical for nonselective cation channels. The potassium channel blockers barium and cesium did not influence the TRH-induced depolarization. TRH effects were antagonized by inhibitors of the Na(+)/Ca(2+) exchanger, KB-R7943 and benzamil. The frequency of GABAergic spontaneous IPSCs was either increased (TTX-insensitive) or decreased [TTX-sensitive spontaneous IPSCs (sIPSCs)] by TRH, indicating a heterogeneous modulation of GABAergic inputs by TRH. Facilitation but not depression of sIPSC frequency by TRH was missing in the presence of the kappa-opioid receptor antagonist nor-binaltorphimine. Montirelin (TRH analog, 1 mg/kg, i.p.) induced waking in wild-type mice but not in histidine decarboxylase knock-out mice lacking histamine. Inhibition of histamine synthesis by (S)-alpha-fluoromethylhistidine blocked the arousal effect of montirelin in wild-type mice. We conclude that direct receptor-mediated excitation of rodent TMN neurons by TRH demands activation of nonselective cation channels as well as electrogenic Na(+)/Ca(2+) exchange. Our findings indicate a key role of the brain histamine system in TRH-induced arousal.
Languageeng
Pub Type(s)Comparative Study
Journal Article
Research Support, Non-U.S. Gov't
PubMed ID19357273
  
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