JBC

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Raghavan, S.
Right arrow Articles by Kanfer, J. N.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Raghavan, S.
Right arrow Articles by Kanfer, J. N.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

Ceramide Galactoside of Enriched Neuronal and Glial Fractions from Rat Brain

Srinivasa Raghavan 1 and Julian N. Kanfer 1

From the 1 Eunice K. Shriver Center for Research in Mental Retardation, W. E. Fernald State School, 200 Trapelo Road, Waltham, Massachusetts 02154 and Neurology Research J. F. Kennedy Jr. Memorial Laboratories, Massachusetts General Hospital, Boston, Massachusetts, 02114

Fractions enriched in neuronal and glial cells from rat brain, as well as myelin isolated from the same brain samples, were analyzed for the composition of cholesterol, phospholipids, cerebrosides, and sulfatides. The fatty acid composition of ceramide galactoside of neurons, glia, and myelin showed significant differences. Less hydroxy fatty acids were recovered from ceramide galactoside obtained from neurons and glia when compared to ceramide galactoside from myelin. The nonhydroxy fatty acids of ceramide galactoside of the two cell types were mainly composed of palmitate and stearate while that of myelin contained longer chain homologs.

Submitted on August 6, 1971


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
J. Neurosci.Home page
I. Zoller, M. Meixner, D. Hartmann, H. Bussow, R. Meyer, V. Gieselmann, and M. Eckhardt
Absence of 2-Hydroxylated Sphingolipids Is Compatible with Normal Neural Development But Causes Late-Onset Axon and Myelin Sheath Degeneration
J. Neurosci., September 24, 2008; 28(39): 9741 - 9754.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
M. Eckhardt, K. K. Hedayati, J. Pitsch, R. Lullmann-Rauch, H. Beck, S. N. Fewou, and V. Gieselmann
Sulfatide Storage in Neurons Causes Hyperexcitability and Axonal Degeneration in a Mouse Model of Metachromatic Leukodystrophy
J. Neurosci., August 22, 2007; 27(34): 9009 - 9021.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 All ASBMB Journals   Molecular and Cellular Proteomics 
 Journal of Lipid Research   ASBMB Today 
Copyright © 1972 by the American Society for Biochemistry and Molecular Biology.