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Tonically active α5GABAa receptors reduce motoneuron excitability and decrease the monosynaptic reflex

  • Martha Canto-Bustos
    ,
  • Emanuel Loeza-Alcocer
    ,
  • ,
  • Paulina Osuna
    ,
  • David Elias-Viñas
    ,
  • Vinicio Granados-Soto
  • University of Pittsburgh
    ,
  • Mayo Clinic Rochester, MN
    ,
  • Centro de Investigacion y de Estudios Avanzados del Instituto Politécnico Nacional
    ,
  • Benemerita Universidad Autonoma de Puebla
Research Output:
Contribution to journal
Article
Peer-review

Open access

Publication Information

Output type

Research Output:
Contribution to journal
Article
Peer-review

Original language

English

Article number

283

Journal (Volume, Issue Number)

Frontiers in Cellular Neuroscience (Volume 11)

Publication milestones

  • Published - 19/09/2017

Publication status

Published - 19/09/2017

ISSN

1662-5102

Publication IDs

  • Scopus: 85032028143

Abstract

Motoneurons, the final common path of the Central Nervous System (CNS), are under a complex control of its excitability in order to precisely translate the interneuronal pattern of activity into skeletal muscle contraction and relaxation. To fulfill this relevant function, motoneurons are provided with a vast repertoire of receptors and channels, including the extrasynaptic GABAA receptors which have been poorly investigated. Here, we confirmed that extrasynaptic α5 subunit-containing GABAA receptors localize with choline acetyltransferase (ChAT) positive cells, suggesting that these receptors are expressed in turtle motoneurons as previously reported in rodents. In these cells, α5GABAA receptors are activated by ambient GABA, producing a tonic shunt that reduces motoneurons’ membrane resistance and affects their action potential firing properties. In addition, α5GABAA receptors shunted the synaptic excitatory inputs depressing the monosynaptic reflex (MSR) induced by activation of primary afferents. Therefore, our results suggest that α5GABAA receptors may play a relevant physiological role in motor control.

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