M-type potassium currents differentially affect activation of motoneuron subtypes and tune recruitment gain

Simon A. Sharples, Matthew J. Broadhead, James Gray, Gareth B. Miles*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

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Abstract

The size principle is a key mechanism governing the orderly recruitment of motor units and is believed to be dependent on passive properties of the constituent motoneurons. However, motoneurons are endowed with voltage-sensitive ion channels that create non-linearities in their input-output functions. Here we describe a role for the M-type potassium current, conducted by KCNQ channels, in the control of motoneuron recruitment in mice. Motoneurons were studied with whole-cell patch clamp electrophysiology in transverse spinal slices and identified based on delayed (fast) and immediate (slow) onsets of repetitive firing. M-currents were larger in delayed compared to immediate firing motoneurons, which was not reflected by variations in the presence of Kv7.2 or Kv7.3 subunits. Instead, a more depolarized spike threshold in delayed-firing motoneurons afforded a greater proportion of the total M-current to become activated within the subthreshold voltage range, which translated to a greater influence on their recruitment with little influence on their firing rates. Pharmacological activation of M-currents also influenced motoneuron recruitment at the population level, producing a rightward shift in the recruitment curve of monosynaptic reflexes within isolated mouse spinal cords. These results demonstrate a prominent role for M-type potassium currents in regulating the function of motor units, which occurs primarily through the differential control of motoneuron subtype recruitment. More generally, these findings highlight the importance of active properties mediated by voltage-sensitive ion channels in the differential control of motoneuron recruitment, which is a key mechanism for the gradation of muscle force.
Original languageEnglish
Pages (from-to)5751-5775
Number of pages25
JournalThe Journal of Physiology
Volume601
Issue number24
Early online date21 Nov 2023
DOIs
Publication statusPublished - 15 Dec 2023

Keywords

  • M-current
  • Motoneuron
  • Recruitment

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