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A3 adenosine receptor agonist reduces brain ischemic injury and inhibits inflammatory cell migration in rats

Title
A3 adenosine receptor agonist reduces brain ischemic injury and inhibits inflammatory cell migration in rats
Authors
Choi I.-Y.Lee J.-C.Ju C.Hwang S.Cho G.-S.Lee H.W.Choi W.J.Jeong L.S.Kim W.-K.
Ewha Authors
정낙신
Issue Date
2011
Journal Title
American Journal of Pathology
ISSN
0002-9440JCR Link
Citation
vol. 179, no. 4, pp. 2042 - 2052
Indexed
SCI; SCIE; SCOPUS WOS scopus
Abstract
A3 adenosine receptor (A3AR) is recognized as a novel therapeutic target for ischemic injury; however, the mechanism underlying anti-ischemic protection by the A3AR agonist remains unclear. Here, we report that 2-chloro-N 6-(3-iodobenzyl)-5′-N-methylcarbamoyl-4′-thioadenosine (LJ529), a selective A3AR agonist, reduces inflammatory responses that may contribute to ischemic cerebral injury. Postischemic treatment with LJ529 markedly reduced cerebral ischemic injury caused by 1.5-hour middle cerebral artery occlusion, followed by 24-hour reperfusion in rats. This effect was abolished by the simultaneous administration of the A3AR antagonist MRS1523, but not the A2AAR antagonist SCH58261. LJ529 prevented the infiltration/migration of microglia and monocytes occurring after middle cerebral artery occlusion and reperfusion, and also after injection of lipopolysaccharides into the corpus callosum. The reduced migration of microglia by LJ529 could be related with direct inhibition of chemotaxis and down-regulation of spatiotemporal expression of Rho GTPases (including Rac, Cdc42, and Rho), rather than by biologically relevant inhibition of inflammatory cytokine/chemokine release (eg, IL-1β, TNF-α, and MCP-1) or by direct inhibition of excitotoxicity/oxidative stress (not affected by LJ529). The present findings indicate that postischemic activation of A3AR and the resultant reduction of inflammatory response should provide a promising therapeutic strategy for the treatment of ischemic stroke. © 2011 American Society for Investigative Pathology.
DOI
10.1016/j.ajpath.2011.07.006
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약학대학 > 약학과 > Journal papers
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