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Na+/Ca2+ exchanger subtype (NCX1, NCX2, NCX3) protein expression in the rat hippocampus following 3 min and 8 min durations of global cerebral ischemia.

Abstract
There is increasing evidence that the sodium-calcium exchanger (NCX) subtypes, NCX1, NCX2 and NCX3 play an important role in intracellular calcium homeostasis/dysregulation following cerebral ischemia. In the present study we examined NCX1, NCX2 and NCX3 protein levels in the rat hippocampus at 3, 6, 12, 18, 24 and 48 h following a 3 min and 8 min duration of global cerebral ischemia. We observed that NCX1 protein levels were significantly increased by 22.3% and 20.6% at the 6 and 12 h respective time points following a 3 min duration of global ischemia, while NCX2 and NCX3 protein levels remained relatively constant. Following a 8 min duration of global ischemia, NCX1 protein levels remained relatively constant, while NCX2 protein levels were down-regulated by 6.9%, 10.8%, 14.4% and 10.3% at the 6, 18, 24 and 48 h respective time points, and NCX3 protein levels were up-regulated by 22.1% at the 18 h time point. Taken together, our results show that NCX subtype protein expression is sensitive to cerebral ischemia, and indicates that changes in NCX activity may be playing an important role in calcium maintenance and neuronal outcome following ischemia.
AuthorsChristina Bojarski, Bruno P Meloni, Stephen R Moore, Bernadette T Majda, Neville W Knuckey
JournalBrain research (Brain Res) Vol. 1189 Pg. 198-202 (Jan 16 2008) ISSN: 0006-8993 [Print] Netherlands
PMID18037393 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Membrane Transport Proteins
  • Slc8a2 protein, rat
  • Slc8a3 protein, rat
  • Sodium-Calcium Exchanger
  • sodium-calcium exchanger 1
Topics
  • Animals
  • Brain Ischemia (metabolism, physiopathology)
  • Calcium Signaling (physiology)
  • Down-Regulation (physiology)
  • Hippocampus (metabolism, physiopathology)
  • Ischemic Preconditioning
  • Male
  • Membrane Transport Proteins (metabolism)
  • Nerve Degeneration (metabolism, physiopathology)
  • Neurons (metabolism)
  • Rats
  • Sodium-Calcium Exchanger (metabolism)
  • Time Factors

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