Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9426718 | Neuroscience | 2005 | 7 Pages |
Abstract
The inflammatory response accompanies and exacerbates the developing injury after cerebral ischemia. Ibuprofen, a non-steroidal anti-inflammatory drug, has been shown to attenuate injuries in animal models of various neurological diseases. In the present study, we investigated ibuprofen's neuroprotective effects in rats exposed to transient forebrain ischemia and in cultures exposed to oxygen glucose deprivation (OGD). Rats treated with ibuprofen after transient forebrain ischemia displayed long-lasting protection of CA1 hippocampal neurons. There were selective increases in interleukin-1 receptor antagonist gene and protein expression in ibuprofen-treated OGD microglia. Furthermore, treatment with ibuprofen in neuron/microglia co-cultures increased the number of surviving HC2S2 neurons against OGD whereas IL-1ra neutralizing antibody reversed the ibuprofen-induced neuroprotection. The data indicate that ibuprofen-induced IL-1ra secretion is involved in neuroprotection against ischemic conditions.
Keywords
CA1 hippocampusBV2IL-1RARPAOGDPPARBV2 microgliaNSAIDDMEMPBS4-VORNAse protection assayIL-1 receptor antagonistfour-vessel occlusionGlobal ischemiaNon-steroidal anti-inflammatory drugNeuroprotectionOxygen glucose deprivationOxygen-glucose deprivationPhosphate-buffered salineDulbecco’s modified eagle’s mediumRatperoxisome proliferators-activated receptor
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Authors
E.-M. Park, B.-P. Cho, B.T. Volpe, M.O. Cruz, T.H. Joh, S. Cho,