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  Lipidomics reveals dysfunctional glycosynapses in schizophrenia and the G72/G30 transgenic mouse

Wood, P. L., Filiou, M. D., Otte, D. M., Zimmer, A., & Turck, C. W. (2014). Lipidomics reveals dysfunctional glycosynapses in schizophrenia and the G72/G30 transgenic mouse. SCHIZOPHRENIA RESEARCH, 159(2-3), 365-369. doi:10.1016/j.schres.2014.08.029.

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 Creators:
Wood, Paul L.1, Author
Filiou, Michaela D.2, Author           
Otte, David M.1, Author
Zimmer, Andreas1, Author
Turck, Christoph W.2, Author           
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1external, ou_persistent22              
2Dept. Translational Research in Psychiatry, Max Planck Institute of Psychiatry, Max Planck Society, ou_2035295              

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 Abstract: Background: Abnormal structural/functional connectivity has been proposed to underlie the pathophysiology of schizophrenia. However, the biochemical basis of abnormal connectivity remains undefined. Methods: We undertook a shotgun lipidomic analysis of over 700 lipids across 26 lipid subclasses in the frontal cortex of schizophrenia subjects and hippocampus of G72/G30 transgenic mice. Results: We demonstrate that glycosphingolipids and choline plasmalogens, structural lipid pools in myelin, are significantly elevated in the frontal cortex obtained from patients suffering from schizophrenia and the hippocampus of G72/G30 transgenic mice. Conclusions: Our data suggest that structural lipid alterations in oligodendrocyte glycosynapses are responsible for dysconnectivity in schizophrenia and that increased expression of G72 protein may play a role in the development of abnormal glycosynapses. (C) 2014 Elsevier B. V. All rights reserved.

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Language(s): eng - English
 Dates: 2014-11
 Publication Status: Issued
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Title: SCHIZOPHRENIA RESEARCH
Source Genre: Journal
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Publ. Info: Amsterdam : Elsevier
Pages: - Volume / Issue: 159 (2-3) Sequence Number: - Start / End Page: 365 - 369 Identifier: ISSN: 0920-9964