Inhibition of Na+/H+ exchanger reduces infarct volume of focal cerebral ischemia in rats

Jiro Kitayama, Takanari Kitazono, Hiroshi Yao, Hiroaki Ooboshi, Hitonori Takaba, Tetsuro Ago, Masatoshi Fujishima, Setsuro Ibayashi

Research output: Contribution to journalArticle

34 Citations (Scopus)

Abstract

Activation of Na+/H+ exchanger (NHE) may have an important role in ischemic cell death by means of intracellular overload of Na+ and Ca2+. Recent evidence has suggested that inhibitors of NHE have protective effects on myocardial ischemia both in vivo and in vitro. In this study, we tested the hypothesis that FR183998, an inhibitor of NHE, reduces infarct volume produced by focal cerebral ischemia in rats. We used 20 male spontaneously hypertensive rats. Either FR183998 (1 mg/kg; n=10), or vehicle (n=10) was given intravenously to the rats and the distal middle cerebral artery of each animal was occluded using a photothrombotic technique. We measured regional cerebral blood flow using laser-Doppler flowmetry throughout the experiments. After 3 days, infarct volume was measured in each animal group. To estimate the brain edema, we also calculated the cortical volume in both hemispheres. The infarct volume in the FR183998-treated group (82±8 mm3, mean±S.E.M.) was significantly smaller than that in the control group (115±12 mm3) (P=0.034). The cortical volume of the occluded side in the FR183998-treated group (359±7 mm3) tended to be smaller than that in the control group (378±9 mm3) (P=0.116). The regional cerebral blood flow and physiological variables during ischemia were not significantly different between the two groups throughout the experiments. These results suggest that inhibition of NHE by FR183998 may have beneficial effects in reducing infarct volume and brain edema during cerebral ischemia. Thus, NHE may play an important role in the development of neuronal damage during acute cerebral ischemia.

Original languageEnglish
Pages (from-to)223-228
Number of pages6
JournalBrain Research
Volume922
Issue number2
DOIs
Publication statusPublished - Dec 20 2001

All Science Journal Classification (ASJC) codes

  • Neuroscience(all)
  • Molecular Biology
  • Clinical Neurology
  • Developmental Biology

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