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Implication of cyclooxygenase-2 on enhanced proliferation of neural progenitor cells in the adult mouse hippocampus after ischemia.

Abstract
Global ischemia promotes neurogenesis in the dentate gyrus of the adult mouse hippocampus. Cyclooxygenase (COX)-2, the principal isoenzyme in the brain, modulates inflammation, glutamate-mediated cytotoxicity, and synaptic plasticity. We demonstrated that delayed treatment with different classes of COX inhibitor significantly blunted enhancement of dentate gyrus proliferation of neural progenitor cells after ischemia. COX-2 immunoreactivity was observed in both neurons and astrocytes in the dentate gyrus, but not in neural progenitor cells in the subgranular zone. Moreover, in the postischemic dentate gyrus of heterozygous and homozygous COX-2 knockout mice, proliferating bromodeoxyuridine-positive cells were significantly fewer than in wild-type littermates. These results demonstrate that COX-2 is an important modulator in enhancement of proliferation of neural progenitor cells after ischemia.
AuthorsTsutomu Sasaki, Kazuo Kitagawa, Shiro Sugiura, Emi Omura-Matsuoka, Shigeru Tanaka, Yoshiki Yagita, Hideyuki Okano, Masayasu Matsumoto, Masatsugu Hori
JournalJournal of neuroscience research (J Neurosci Res) Vol. 72 Issue 4 Pg. 461-71 (May 15 2003) ISSN: 0360-4012 [Print] United States
PMID12704808 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright 2003 Wiley-Liss, Inc.
Chemical References
  • Cyclooxygenase 2 Inhibitors
  • Cyclooxygenase Inhibitors
  • Isoenzymes
  • Nitrobenzenes
  • Sulfonamides
  • N-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide
  • Cyclooxygenase 2
  • Prostaglandin-Endoperoxide Synthases
  • Indomethacin
Topics
  • Animals
  • Astrocytes (drug effects, enzymology)
  • Brain Ischemia (enzymology, genetics, physiopathology)
  • Cell Differentiation (genetics, physiology)
  • Cell Division (drug effects, genetics, physiology)
  • Cyclooxygenase 2
  • Cyclooxygenase 2 Inhibitors
  • Cyclooxygenase Inhibitors (pharmacology)
  • Hippocampus (cytology, drug effects, enzymology)
  • Immunohistochemistry
  • Indomethacin (pharmacology)
  • Isoenzymes (antagonists & inhibitors, genetics, metabolism)
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Neurons (drug effects, enzymology)
  • Nitrobenzenes (pharmacology)
  • Prostaglandin-Endoperoxide Synthases (genetics, metabolism)
  • Stem Cells (drug effects, enzymology)
  • Sulfonamides (pharmacology)

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