Literature DB >> 15730878

Distinct roles of glycinergic and GABAergic inhibition in coordinating locomotor-like rhythms in the neonatal mouse spinal cord.

C Hinckley1, B Seebach, L Ziskind-Conhaim.   

Abstract

The primary objective of our study was to examine the role of the inhibitory neurotransmitters glycine and GABA in modulating spontaneous activity and coordinating neurochemically induced locomotor-like rhythms in the mouse spinal cord. Motor outputs were recorded in lumbar ventral roots of 1-4-day old neonatal mice, and the function of glycinergic and GABAergic synapses in regulating spontaneous and induced activities was examined by suppressing synaptic inhibition using selective glycine or GABAA receptor antagonists. Strychnine (0.5 microM), a glycine receptor antagonist, did not change the pattern of spontaneous activity that consisted of random single spikes and discharges of variable durations and intervals. In contrast, blocking GABAA receptors with either picrotoxin (10 microM) or bicuculline (5 microM) triggered bilaterally synchronous, non-rhythmic discharges. These findings suggested that GABAergic synapses suppressed excitatory synapses, and their disinhibition synchronized spontaneous discharges between the two sides of the spinal cord. Locomotor-like rhythms alternating between the two sides of the spinal cord were triggered by the neurotransmitter agonists 5-HT, N-methyl-D,L-aspartic acid and dopamine. Blocking glycine receptors increased tonic discharges, and in most preparations it reduced the phase correlation between the alternating rhythms. Inhibiting GABAA receptor-mediated synapses synchronized the onset and prolonged the duration of rhythmic discharges. Intraburst alternating peaks were evident and those were suppressed by strychnine, suggesting that they were mediated via glycinergic synapses. Our findings indicated that GABAergic and glycinergic synapses played different roles in modulating neurochemically induced locomotion rhythms. GABAergic inhibition regulated the onset and duration of neurochemically induced locomotor-like rhythms, and glycinergic inhibition stabilized the pattern of the alternating rhythms.

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Year:  2005        PMID: 15730878     DOI: 10.1016/j.neuroscience.2004.11.034

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  25 in total

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3.  NKCC1 cotransporter inactivation underlies embryonic development of chloride-mediated inhibition in mouse spinal motoneuron.

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Journal:  J Physiol       Date:  2007-12-20       Impact factor: 5.182

4.  Segmental, synaptic actions of commissural interneurons in the mouse spinal cord.

Authors:  Katharina A Quinlan; Ole Kiehn
Journal:  J Neurosci       Date:  2007-06-13       Impact factor: 6.167

5.  Persistent sodium current contributes to induced voltage oscillations in locomotor-related hb9 interneurons in the mouse spinal cord.

Authors:  Lea Ziskind-Conhaim; Linying Wu; Eric P Wiesner
Journal:  J Neurophysiol       Date:  2008-07-30       Impact factor: 2.714

6.  Progressive changes in synaptic inputs to motoneurons in adult sacral spinal cord of a mouse model of amyotrophic lateral sclerosis.

Authors:  Mingchen Jiang; Jenna E Schuster; Ronggen Fu; Teepu Siddique; C J Heckman
Journal:  J Neurosci       Date:  2009-12-02       Impact factor: 6.167

7.  The specification of glycinergic neurons and the role of glycinergic transmission in development.

Authors:  Alexander V Chalphin; Margaret S Saha
Journal:  Front Mol Neurosci       Date:  2010-04-22       Impact factor: 5.639

8.  Glutamatergic mechanisms for speed control and network operation in the rodent locomotor CpG.

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9.  Sensitivity of spinal neurons to GABA and glycine during voluntary movement in behaving monkeys.

Authors:  Guoji Wu; Steve I Perlmutter
Journal:  J Neurophysiol       Date:  2012-10-17       Impact factor: 2.714

Review 10.  Diversity of molecularly defined spinal interneurons engaged in mammalian locomotor pattern generation.

Authors:  Lea Ziskind-Conhaim; Shawn Hochman
Journal:  J Neurophysiol       Date:  2017-08-30       Impact factor: 2.714

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