Specificity of carbohydrate structures of gangliosides in the activity to regenerate the rat axotomized hypoglossal nerve
Glycobiology, ISSN: 0959-6658, Vol: 11, Issue: 2, Page: 125-130
2001
- 20Citations
- 9Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations20
- Citation Indexes20
- 20
- CrossRef14
- Captures9
- Readers9
Article Description
We previously reported that a ganglioside mixture from bovine brain could prevent neuronal death and promote regeneration in rats with hypoglossal nerve resection. In the present study, we have compared the neurotrophic effects of various glycosphingolipids including lactosylceramide. The findings revealed that GT1b had the activity of neuronal death prevention equivalent to a ganglioside mixture or autograft, while other glycolipids exhibited about 60% activity. However, the capability to promote the regeneration varied among glycolipids, that is, GT1b (86%), GD1b (55%), GD1a (35%), GQ1b (34%), GM1 (20%), lactosyl-ceramide (17%) in the number of horseradish peroxidase-positive neurons as an indicator of regeneration. The experiments with oligosaccharides of GT1b or GD1b and ceramide showed that the carbohydrate moiety mainly exerts neurotrophic effects. These findings suggested that fine structures of carbohydrate moiety in gangliosides are critical in the regenerative activity in this hypoglossal nerve regeneration system.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0035058283&origin=inward; http://dx.doi.org/10.1093/glycob/11.2.125; http://www.ncbi.nlm.nih.gov/pubmed/11287399; https://academic.oup.com/glycob/article-lookup/doi/10.1093/glycob/11.2.125; https://dx.doi.org/10.1093/glycob/11.2.125; https://academic.oup.com/glycob/article/11/2/125/552884
Oxford University Press (OUP)
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