Literature DB >> 9037391

Ganglioside composition of the human cranial nerves, with special reference to pathophysiology of Miller Fisher syndrome.

A Chiba1, S Kusunoki, H Obata, R Machinami, I Kanazawa.   

Abstract

Total ganglioside fractions from the human cranial nerves purified on a Phenyl Sepharose column, were given mild alkaline treatment, after which their composition and amounts of lipid-bound sialic acid were determined by HPTLC-densitometry with resorcinol as the coloring reagent. The total amounts of lipid-bound sialic acid were 156.5 ng/mg of wet tissue in the Ist cranial nerve (olfactory tract) and 131.9 ng/mg in the IInd nerve, greater than the amounts in the other nerves (99.1-120.0 ng/mg). The Ist, IInd, and VIIIth nerves had GM4, but not LM1. It may reflect their histological feature of the central nervous system. The IIIrd, IVth, and VIth nerves, as well as the IInd, had significantly higher percentages of GQ1b (11.6-13.2%) than the other nerves (5.2-8.4%). The high proportion of GQ1b specific to these three cranial nerves involved in the ocular movement lends support to the role of serum anti-GQ1b antibody in the pathogenetic mechanisms of ophthalmoplegia in Miller Fisher syndrome and Guillain-Barré syndrome.

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Year:  1997        PMID: 9037391     DOI: 10.1016/s0006-8993(96)01123-7

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


  43 in total

Review 1.  Guillain Barré syndrome.

Authors:  J B Winer
Journal:  Mol Pathol       Date:  2001-12

2.  Expression machinery of GM4: the excess amounts of GM3/GM4S synthase (ST3GAL5) are necessary for GM4 synthesis in mammalian cells.

Authors:  Satoshi Uemura; Shinji Go; Fumi Shishido; Jin-ichi Inokuchi
Journal:  Glycoconj J       Date:  2013-09-03       Impact factor: 2.916

Review 3.  [Miller Fisher syndrome: case report and review with discussion of differential diagnosis and nosology].

Authors:  U Becker; G Gahn; H Reichmann; B Herting
Journal:  Nervenarzt       Date:  2006-06       Impact factor: 1.214

4.  Optic neuritis as a possible phenotype of anti-GQ1b/GT1a antibody syndrome.

Authors:  Damien Biotti; Sophie Boucher; Elodie Ong; Caroline Tilikete; Alain Vighetto
Journal:  J Neurol       Date:  2013-09-06       Impact factor: 4.849

Review 5.  Neuro-ophthalmology and the Anti-GQ1b antibody syndromes.

Authors:  Robert F Saul
Journal:  Curr Neurol Neurosci Rep       Date:  2009-09       Impact factor: 5.081

Review 6.  Pathophysiological actions of neuropathy-related anti-ganglioside antibodies at the neuromuscular junction.

Authors:  Jaap J Plomp; Hugh J Willison
Journal:  J Physiol       Date:  2009-06-29       Impact factor: 5.182

Review 7.  Clinical utility of autoantibodies in Guillain-Barre syndrome and its variants.

Authors:  J W Terryberry; Y Shoenfeld; J B Peter
Journal:  Clin Rev Allergy Immunol       Date:  1998       Impact factor: 8.667

8.  Acute bulbar palsy without ophtalmoplegia associated with anti-GD3 IgM antibodies.

Authors:  Stefania Barone; Salvatore Maria Cavalli; Marco Casaletto; Aldo Quattrone; Angelo Labate
Journal:  Neurol Sci       Date:  2016-11-11       Impact factor: 3.307

9.  Anti-GM2 ganglioside antibodies are a biomarker for acute canine polyradiculoneuritis.

Authors:  Angie Rupp; Francesc Galban-Horcajo; Ezio Bianchi; Maurizio Dondi; Jacques Penderis; Joanna Cappell; Karl Burgess; Kaspar Matiasek; Rhona McGonigal; Hugh J Willison
Journal:  J Peripher Nerv Syst       Date:  2013-03       Impact factor: 3.494

10.  Acute paretic syndrome in juvenile White Leghorn chickens resembles late stages of acute inflammatory demyelinating polyneuropathies in humans.

Authors:  Sophie R Bader; Sonja Kothlow; Sascha Trapp; Susanne Cn Schwarz; Hans-Christian Philipp; Steffen Weigend; Ahmad R Sharifi; Rudolf Preisinger; Wolfgang Schmahl; Bernd Kaspers; Kaspar Matiasek
Journal:  J Neuroinflammation       Date:  2010-01-28       Impact factor: 8.322

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