Literature DB >> 1726063

A glycinergic projection from the ventromedial lower brainstem to spinal motoneurons. An ultrastructural double labeling study in rat.

J C Holstege1, C M Bongers.   

Abstract

In the present study it was determined whether glycine was present in the descending brainstem projections to spinal motoneurons in the rat. For this purpose injections of wheatgerm agglutinin-horseradish peroxidase (WGA-HRP) were made in the ventromedial part of the lower brainstem at the levels of the rostral inferior olive and the caudal facial nucleus. After perfusion, WGA-HRP histochemistry was performed, followed by the postembedding immunogold technique with an antibody against glycine. Electron microscopical examination of the lumbar motoneuronal cell groups showed that 15% of the WGA-HRP labeled terminals, derived from the ventromedial reticular formation, were also labeled for glycine. The majority (91%) of these double labeled terminals were of the F-type (containing many flattened vesicles), while the remaining 9% were of the S-type (containing mostly spherical vesicles). Many of the double labeled terminals established a synapse, mostly with proximal and distal dendrites. The present data, combined with our previous findings that 40% of the projections from the same ventromedial brainstem area to lumbar motoneurons contained gamma-aminobutyric acid (GABA), indicate that over 50% of these brainstem projections contain GABA and/or glycine, exerting a direct inhibitory effect on spinal motoneurons. The possibility that the glycinergic fibers within these projections play an important role in producing muscle atonia during rapid eye movement (REM) sleep is discussed.

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Year:  1991        PMID: 1726063     DOI: 10.1016/0006-8993(91)91715-d

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  28 in total

1.  Glycine-mediated postsynaptic inhibition is responsible for REM sleep atonia.

Authors:  Peter J Soja
Journal:  Sleep       Date:  2008-11       Impact factor: 5.849

2.  Fine structure of the interstitial nucleus of Cajal of the cat.

Authors:  R Bianchi; M Gioia
Journal:  J Anat       Date:  1995-08       Impact factor: 2.610

3.  Arterial tortuosity in the femoropopliteal region during knee flexion: a magnetic resonance angiographic study.

Authors:  P J Wensing; F G Scholten; P C Buijs; M J Hartkamp; W P Mali; B Hillen
Journal:  J Anat       Date:  1995-08       Impact factor: 2.610

4.  The sleep-promoting and hypothermic effects of glycine are mediated by NMDA receptors in the suprachiasmatic nucleus.

Authors:  Nobuhiro Kawai; Noriaki Sakai; Masashi Okuro; Sachie Karakawa; Yosuke Tsuneyoshi; Noriko Kawasaki; Tomoko Takeda; Makoto Bannai; Seiji Nishino
Journal:  Neuropsychopharmacology       Date:  2014-12-23       Impact factor: 7.853

5.  A Discrete Glycinergic Neuronal Population in the Ventromedial Medulla That Induces Muscle Atonia during REM Sleep and Cataplexy in Mice.

Authors:  Shuntaro Uchida; Shingo Soya; Yuki C Saito; Arisa Hirano; Keisuke Koga; Makoto Tsuda; Manabu Abe; Kenji Sakimura; Takeshi Sakurai
Journal:  J Neurosci       Date:  2020-12-28       Impact factor: 6.167

Review 6.  Control of sleep and wakefulness.

Authors:  Ritchie E Brown; Radhika Basheer; James T McKenna; Robert E Strecker; Robert W McCarley
Journal:  Physiol Rev       Date:  2012-07       Impact factor: 37.312

7.  Ventral medullary control of rapid eye movement sleep and atonia.

Authors:  Michael C Chen; Ramalingam Vetrivelan; Chun-Ni Guo; Catie Chang; Patrick M Fuller; Jun Lu
Journal:  Exp Neurol       Date:  2017-01-07       Impact factor: 5.330

Review 8.  Serotonergic transmission after spinal cord injury.

Authors:  Raffaele Nardone; Yvonne Höller; Aljoscha Thomschewski; Peter Höller; Piergiorgio Lochner; Stefan Golaszewski; Francesco Brigo; Eugen Trinka
Journal:  J Neural Transm (Vienna)       Date:  2014-05-28       Impact factor: 3.575

9.  Medullary circuitry regulating rapid eye movement sleep and motor atonia.

Authors:  Ramalingam Vetrivelan; Patrick M Fuller; Qingchun Tong; Jun Lu
Journal:  J Neurosci       Date:  2009-07-22       Impact factor: 6.167

10.  State-dependent changes in glutamate, glycine, GABA, and dopamine levels in cat lumbar spinal cord.

Authors:  N Taepavarapruk; P Taepavarapruk; J John; Y Y Lai; J M Siegel; A G Phillips; S A McErlane; P J Soja
Journal:  J Neurophysiol       Date:  2008-03-19       Impact factor: 2.714

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