Literature DB >> 18353915

Whisker movements evoked by stimulation of single motor neurons in the facial nucleus of the rat.

Lucas J Herfst1, Michael Brecht.   

Abstract

The lateral facial nucleus is the sole output structure whose neuronal activity leads to whisker movements. To understand how single facial nucleus neurons contribute to whisker movement we combined single-cell stimulation and high-precision whisker tracking. Half of the 44 stimulated neurons gave rise to fast whisker protraction or retraction movement, whereas no stimulation-evoked movements could be detected for the remainder. Direction, speed, and amplitude of evoked movements varied across neurons. Protraction movements were more common than retraction movements (n = 16 vs. n = 4), had larger amplitudes (1.8 vs. 0.3 degrees for single spike events), and most protraction movements involved only a single whisker, whereas most retraction movements involved multiple whiskers. We found a large range in the amplitude of single spike-evoked whisker movements (0.06-5.6 degrees ). Onset of the movement occurred at 7.6 (SD 2.5) ms after the spike and the time to peak deflection was 18.2 (SD 4.3) ms. Each spike reliably evoked a stereotyped movement. In two of five cases peak whisker deflection resulting from consecutive spikes was larger than expected when based on linear summation of single spike-evoked movement profiles. Our data suggest the following coding scheme for whisker movements in the facial nucleus. 1) Evoked movement characteristics depend on the identity of the stimulated neuron (a labeled line code). 2) The facial nucleus neurons are heterogeneous with respect to the movement properties they encode. 3) Facial nucleus spikes are translated in a one-to-one manner into whisker movements.

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Mesh:

Year:  2008        PMID: 18353915     DOI: 10.1152/jn.01014.2007

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  28 in total

1.  Friction-based stabilization of juxtacellular recordings in freely moving rats.

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Journal:  Prog Neurobiol       Date:  2012-01-28       Impact factor: 11.685

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Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2015-09-19       Impact factor: 6.237

4.  Identification of single neurons in a forebrain network.

Authors:  Nancy F Day; Stephen J Kerrigan; Naoya Aoki; Teresa A Nick
Journal:  J Neurophysiol       Date:  2011-09-07       Impact factor: 2.714

5.  Parallel Inhibitory and Excitatory Trigemino-Facial Feedback Circuitry for Reflexive Vibrissa Movement.

Authors:  Marie-Andrée Bellavance; Jun Takatoh; Jinghao Lu; Maxime Demers; David Kleinfeld; Fan Wang; Martin Deschênes
Journal:  Neuron       Date:  2017-07-20       Impact factor: 17.173

6.  Temporally precise control of single-neuron spiking by juxtacellular nanostimulation.

Authors:  Maik C Stüttgen; Lourens J P Nonkes; H Rüdiger A P Geis; Paul H Tiesinga; Arthur R Houweling
Journal:  J Neurophysiol       Date:  2017-01-11       Impact factor: 2.714

7.  Pre-neuronal morphological processing of object location by individual whiskers.

Authors:  Knarik Bagdasarian; Marcin Szwed; Per Magne Knutsen; Dudi Deutsch; Dori Derdikman; Maciej Pietr; Erez Simony; Ehud Ahissar
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Review 8.  Bidirectional learning in upbound and downbound microzones of the cerebellum.

Authors:  Chris I De Zeeuw
Journal:  Nat Rev Neurosci       Date:  2020-11-17       Impact factor: 34.870

9.  Automated light-based mapping of motor cortex by photoactivation of channelrhodopsin-2 transgenic mice.

Authors:  Oliver G S Ayling; Thomas C Harrison; Jamie D Boyd; Alexander Goroshkov; Timothy H Murphy
Journal:  Nat Methods       Date:  2009-02-15       Impact factor: 28.547

10.  Synaptic theory of replicator-like melioration.

Authors:  Yonatan Loewenstein
Journal:  Front Comput Neurosci       Date:  2010-06-17       Impact factor: 2.380

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