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A synthetic ceramide analog (L-PDMP) up-regulates neuronal function.

Abstract
To address the role of brain gangliosides in synaptic activity, the ceramide analogs, D-threo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol (D-PDMP) and its enantiomer, L-PDMP, were used to inhibit and stimulate ganglioside biosynthesis in cultured cortical neurons. Prolonged treatment with both PDMP isomers exhibited opposite effects on functional synapse formation measured by spontaneous synchronized oscillatory activity of intracellular Ca2+ between the neurons: suppression by D-PDMP and facilitation by L-PDMP. Up-regulation of synaptic activity by L-PDMP could be correlated with the slow but robust activation of p42 mitogen-activated protein kinase. Treatment with L-PDMP after transient forebrain ischemia in rats ameliorated the deficit of a well-learned spatial memory by an 8-arm maze task, suggesting a new potential therapeutic approach for neurodegenerative disorders.
AuthorsJ Inokuchi, A Mizutani, M Jimbo, S Usuki, K Yamagishi, H Mochizuki, K Muramoto, K Kobayashi, Y Kuroda, K Iwasaki, Y Ohgami, M Fujiwara
JournalAnnals of the New York Academy of Sciences (Ann N Y Acad Sci) Vol. 845 Pg. 219-24 (Jun 19 1998) ISSN: 0077-8923 [Print] United States
PMID9668355 (Publication Type: Journal Article)
Chemical References
  • Enzyme Inhibitors
  • Gangliosides
  • Morpholines
  • RV 538
  • Mitogen-Activated Protein Kinase 1
  • Calcium
Topics
  • Animals
  • Calcium (metabolism)
  • Cells, Cultured
  • Cerebral Cortex (cytology, physiology)
  • Enzyme Inhibitors (pharmacology)
  • Gangliosides (metabolism)
  • Memory (drug effects)
  • Mice
  • Mitogen-Activated Protein Kinase 1 (metabolism)
  • Morpholines (pharmacology)
  • Neurons (drug effects, physiology)
  • Rats
  • Stereoisomerism
  • Synapses (drug effects, physiology)

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