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.
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Authors | Yong Liu, Xiao-Yu Hou, Guang-Yi Zhang, Tian-Le Xu |
Journal | Brain research
(Brain Res)
Vol. 972
Issue 1-2
Pg. 142-8
(May 16 2003)
ISSN: 0006-8993 [Print] Netherlands |
PMID | 12711087
(Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)
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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
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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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