Literature DB >> 1629765

Excitation of motoneurons by the Mauthner axon in goldfish: complexities in a "simple" reticulospinal pathway.

J R Fetcho1.   

Abstract

1. The Mauthner cell in fish and amphibians initiates an escape behavior that has served as a model system for studies of the reticulospinal control of movement. This behavior consists of a very rapid bend of the body and tail that is thought to arise from the monosynaptic excitation of large primary motoneurons by the Mauthner cell. Recent work suggests that the excitation of primary motoneurons might be more complex than a solely monosynaptic connection. To examine this possibility, I used intracellular recording and staining to study the excitation of primary motoneurons by the M cell. 2. Simultaneous intracellular recordings from the M axon and ipsilateral primary motoneurons show that firing the M cell leads to complex postsynaptic potentials (PSPs) in the motoneurons. These PSPs usually have three components: an early, small, slow depolarization (component 1), a later, large, fast depolarization (component 2), and an even later, large, long-lasting depolarization (component 3). The first component has a latency of 0.52 +/- 0.15 (SD) ms, (n = 27) and most probably is a monosynaptic input from the M cell. This study focused on the two subsequent, less-understood parts of the PSP. Motoneurons typically fire off the second part of the PSP. This is usually (27 of 33 cells) the largest component, and it has a mean amplitude of 6.24 +/- 3.33 (SD) mV (n = 33) and a half-decay time of 0.44 +/- 0.18 (SD) ms (n = 27). The mean amplitude of the third component is 3.20 +/- 1.7 (SD) mV (n = 35), and its half-decay is 6.73 +/- 2.66 (SD) ms (n = 35). The latency of the second component averages 0.66 +/- 0.21 (SD) ms (n = 32), indicating that there are few synapses in the pathway mediating it. 3. One candidate pathway for the second component of the PSP involves a class of descending interneurons (DIs) that are monosynaptically, chemically excited by the M cell and appear in light microscopy to contact motoneurons. Simultaneous intracellular recordings from the M axon, a DI, and a primary motoneuron show that the interneurons are electrotonically coupled to motoneurons and produce the fast, second component of the PSP. Direct excitation of an interneuron leads to a very short-latency (less than 0.2 ms), fast PSP in a motoneuron similar to the second component of the PSP produced by the M axon. The short latency and fatigue resistance of this connection indicate it is electrotonic, and this is supported by evidence for DC coupling between the two cells.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1992        PMID: 1629765     DOI: 10.1152/jn.1992.67.6.1574

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


  10 in total

1.  In vivo imaging of zebrafish reveals differences in the spinal networks for escape and swimming movements.

Authors:  D A Ritter; D H Bhatt; J R Fetcho
Journal:  J Neurosci       Date:  2001-11-15       Impact factor: 6.167

2.  Some principles of organization of spinal neurons underlying locomotion in zebrafish and their implications.

Authors:  Joseph R Fetcho; David L McLean
Journal:  Ann N Y Acad Sci       Date:  2010-06       Impact factor: 5.691

3.  Origin of excitation underlying locomotion in the spinal circuit of zebrafish.

Authors:  Emma Eklöf-Ljunggren; Sabine Haupt; Jessica Ausborn; Ivar Dehnisch; Per Uhlén; Shin-ichi Higashijima; Abdeljabbar El Manira
Journal:  Proc Natl Acad Sci U S A       Date:  2012-03-19       Impact factor: 11.205

4.  Some voluntary C-bends may be Mauthner neuron initiated.

Authors:  James G Canfield
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2007-08-03       Impact factor: 1.836

5.  Direct activation of the Mauthner cell by electric field pulses drives ultrarapid escape responses.

Authors:  Kathryn M Tabor; Sadie A Bergeron; Eric J Horstick; Diana C Jordan; Vilma Aho; Tarja Porkka-Heiskanen; Gal Haspel; Harold A Burgess
Journal:  J Neurophysiol       Date:  2014-05-21       Impact factor: 2.714

6.  Differences in the morphology of spinal V2a neurons reflect their recruitment order during swimming in larval zebrafish.

Authors:  Evdokia Menelaou; Cassandra VanDunk; David L McLean
Journal:  J Comp Neurol       Date:  2014-04-15       Impact factor: 3.215

7.  High speed coding for velocity by archerfish retinal ganglion cells.

Authors:  Viola Kretschmer; Friedrich Kretschmer; Malte T Ahlers; Josef Ammermüller
Journal:  BMC Neurosci       Date:  2012-06-18       Impact factor: 3.288

8.  Prepontine non-giant neurons drive flexible escape behavior in zebrafish.

Authors:  Gregory D Marquart; Kathryn M Tabor; Sadie A Bergeron; Kevin L Briggman; Harold A Burgess
Journal:  PLoS Biol       Date:  2019-10-15       Impact factor: 8.029

9.  A specialized spinal circuit for command amplification and directionality during escape behavior.

Authors:  Na N Guan; Lulu Xu; Tianrui Zhang; Chun-Xiao Huang; Zhen Wang; Elin Dahlberg; Haoyu Wang; Fangfang Wang; Irene Pallucchi; Yunfeng Hua; Abdeljabbar El Manira; Jianren Song
Journal:  Proc Natl Acad Sci U S A       Date:  2021-10-19       Impact factor: 11.205

10.  A forward genetic screen identifies Dolk as a regulator of startle magnitude through the potassium channel subunit Kv1.1.

Authors:  Joy H Meserve; Jessica C Nelson; Kurt C Marsden; Jerry Hsu; Fabio A Echeverry; Roshan A Jain; Marc A Wolman; Alberto E Pereda; Michael Granato
Journal:  PLoS Genet       Date:  2021-06-01       Impact factor: 5.917

  10 in total

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