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L-type voltage-gated calcium channel attends regulation of tyrosine phosphorylation of NMDA receptor subunit 2A induced by transient brain ischemia.

Abstract
To study the mechanism of the L-type voltage-gated calcium channel (L-VGCC) involved in neuronal injury induced by brain ischemia and reperfusion (I/R), transient (15 min) brain ischemia was induced by four-vessel occlusion of Sprague-Dawley (SD) rats. Tyrosine phosphorylation of NR2A and interaction of NR2A with Src and Pyk2 in hippocampus induced by brain ischemia and reperfusion (I/R) were determined by immunoprecipitation and immunoblot(ting). Tyrosine phosphorylation of NR2A in hippocampus was enhanced after I/R. Interaction of NR2A with Src and Pyk2, tyrosine phosphorylation and kinase activity of Src and Pyk2 also increased after I/R. All the increases were partly inhibited by L-VGCC antagonist nifedipine administered to rats 20 min prior to brain ischemia. The results suggested that increase of tyrosine phosphorylation of NR2A induced by I/R had a relation to activation of L-VGCC. Src and Pyk2 interacting with NR2A might also be involved in this regulation of the tyrosine phosphorylation of NR2A induced by I/R.
AuthorsYong Liu, Xiao-Yu Hou, Guang-Yi Zhang, Tian-Le Xu
JournalBrain research (Brain Res) Vol. 972 Issue 1-2 Pg. 142-8 (May 16 2003) ISSN: 0006-8993 [Print] Netherlands
PMID12711087 (Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Calcium Channel Blockers
  • Calcium Channels, L-Type
  • Phosphorus Isotopes
  • Receptors, N-Methyl-D-Aspartate
  • Phosphotyrosine
  • Tyrosine
  • Protein-Tyrosine Kinases
  • Focal Adhesion Kinase 2
  • Ptk2b protein, rat
  • src-Family Kinases
  • Nifedipine
  • N-methyl D-aspartate receptor subtype 2A
Topics
  • Animals
  • Brain Ischemia (metabolism)
  • Calcium Channel Blockers (pharmacology)
  • Calcium Channels, L-Type (drug effects, metabolism)
  • Dose-Response Relationship, Drug
  • Focal Adhesion Kinase 2
  • Hippocampus (drug effects, metabolism, physiopathology)
  • Immunoblotting (methods)
  • Male
  • Nifedipine (pharmacology)
  • Phosphorus Isotopes (metabolism)
  • Phosphotyrosine (metabolism)
  • Precipitin Tests (methods)
  • Protein-Tyrosine Kinases (drug effects, metabolism)
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, N-Methyl-D-Aspartate (drug effects, metabolism)
  • Reperfusion (methods)
  • Tyrosine (metabolism)
  • src-Family Kinases (drug effects, metabolism)

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