Identification of minimal neuronal networks involved in flexor-extensor alternation in the mammalian spinal cord

Neuron. 2011 Sep 22;71(6):1071-84. doi: 10.1016/j.neuron.2011.07.011. Epub 2011 Sep 21.

Abstract

Neural networks in the spinal cord control two basic features of locomotor movements: rhythm generation and pattern generation. Rhythm generation is generally considered to be dependent on glutamatergic excitatory neurons. Pattern generation involves neural circuits controlling left-right alternation, which has been described in great detail, and flexor-extensor alternation, which remains poorly understood. Here, we use a mouse model in which glutamatergic neurotransmission has been ablated in the locomotor region of the spinal cord. The isolated in vitro spinal cord from these mice produces locomotor-like activity-when stimulated with neuroactive substances-with prominent flexor-extensor alternation. Under these conditions, unlike in control mice, networks of inhibitory interneurons generate the rhythmic activity. In the absence of glutamatergic synaptic transmission, the flexor-extensor alternation appears to be generated by Ia inhibitory interneurons, which mediate reciprocal inhibition from muscle proprioceptors to antagonist motor neurons. Our study defines a minimal inhibitory network that is needed to produce flexor-extensor alternation during locomotion.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Action Potentials / physiology
  • Animals
  • GABA Antagonists / pharmacology
  • Glutamic Acid / metabolism
  • Glycine / metabolism
  • Glycine Agents / pharmacology
  • Interneurons / physiology
  • Mice
  • Mice, Knockout
  • Motor Activity / physiology*
  • Motor Neurons / drug effects
  • Motor Neurons / physiology*
  • Muscle Contraction / physiology*
  • Muscle, Skeletal / innervation
  • Muscle, Skeletal / physiology
  • Nerve Net / anatomy & histology*
  • Nerve Net / physiology*
  • Periodicity*
  • Picrotoxin / pharmacology
  • Receptors, GABA-A / metabolism
  • Receptors, Glycine / metabolism
  • Spinal Cord / cytology
  • Spinal Cord / physiology*
  • Strychnine / pharmacology
  • Synaptic Transmission / drug effects
  • Synaptic Transmission / physiology
  • Vesicular Glutamate Transport Protein 2 / genetics
  • Vesicular Glutamate Transport Protein 2 / metabolism
  • gamma-Aminobutyric Acid / metabolism

Substances

  • GABA Antagonists
  • Glycine Agents
  • Receptors, GABA-A
  • Receptors, Glycine
  • Slc17a6 protein, mouse
  • Vesicular Glutamate Transport Protein 2
  • Picrotoxin
  • Glutamic Acid
  • gamma-Aminobutyric Acid
  • Strychnine
  • Glycine