4.7 Article

Motor Neurons Tune Premotor Activity in a Vertebrate Central Pattern Generator

Journal

JOURNAL OF NEUROSCIENCE
Volume 37, Issue 12, Pages 3264-3275

Publisher

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.2755-16.2017

Keywords

CPG; feedback; synchrony; vocal; vocalization; Xenopus

Categories

Funding

  1. National Institutes of Health [NS091977]
  2. Reed College startup funds
  3. Direct For Biological Sciences
  4. Division Of Integrative Organismal Systems [1557945] Funding Source: National Science Foundation

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Central patterns generators (CPGs) are neural circuits that drive rhythmic motor output without sensory feedback. Vertebrate CPGs are generally believed to operate in a top-down manner in which premotor interneurons activate motor neurons that in turn drive muscles. In contrast, the frog (Xenopus laevis) vocal CPG contains a functionally unexplored neuronal projection from the motor nucleus to the premotor nucleus, indicating a recurrent pathway that may contribute to rhythm generation. In this study, we characterized the function of this bottom-up connection. The X. laevis vocal CPG produces a 50-60 Hz fast trill song used by males during courtship. We recorded fictive vocalizations in the in vitro CPG from the laryngeal nerve while simultaneously recording premotor activity at the population and single-cell level. We show that transecting the motor-to-premotor projection eliminated the characteristic firing rate of premotor neurons. Silencing motor neurons with the intracellular sodium channel blocker QX-314 also disrupted premotor rhythms, as did blockade of nicotinic synapses in the motor nucleus (the putative location of motor neuron-to-interneuron connections). Electrically stimulating the laryngeal nerve elicited primarily IPSPs in premotor neurons that could be blocked by a nicotinic receptor antagonist. Our results indicate that an inhibitory signal, activated by motor neurons, is required for proper CPG function. To our knowledge, these findings represent the first example of a CPG in which precise premotor rhythms are tuned by motor neuron activity.

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