{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,15]],"date-time":"2026-05-15T03:13:51Z","timestamp":1778814831661,"version":"3.51.4"},"reference-count":68,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[2013,12,6]],"date-time":"2013-12-06T00:00:00Z","timestamp":1386288000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Glia"],"published-print":{"date-parts":[[2014,2]]},"abstract":"<jats:p>Adenosine receptor activation is involved in myelination and in apoptotic pathways linked to neurodegenerative diseases. In this study, we investigated the effects of adenosine receptor activation in the viability of oligodendrocytes of the rat optic nerve. Selective activation of A<jats:sub>3<\/jats:sub> receptors in pure cultures of oligodendrocytes caused concentration\u2010dependent apoptotic and necrotic death which was preceded by oxidative stress and mitochondrial membrane depolarization. Oligodendrocyte apoptosis induced by A<jats:sub>3<\/jats:sub> receptor activation was caspase\u2010dependent and caspase\u2010independent. In addition to dissociated cultures, incubation of optic nerves <jats:italic>ex vivo<\/jats:italic> with adenosine and the A<jats:sub>3<\/jats:sub> receptor agonist 2\u2010CI\u2010IB\u2010MECA(1\u2010[2\u2010Chloro\u20106\u2010[[(3\u2010iodophenyl)methyl]amino]\u20109H\u2010purin\u20109\u2010yl]\u20101\u2010deoxy\u2010N\u2010methyl\u2010b\u2010D\u2010ribofuranuronamide)\u2010induced caspase\u20103 activation, oligodendrocyte damage, and myelin loss, effects which were prevented by the presence of caffeine and the A<jats:sub>3<\/jats:sub> receptor antagonist MRS 1220 (N\u2010[9\u2010Chloro\u20102\u2010(2\u2010furanyl)[1,2,4]\u2010triazolo [1,5\u2010c]quinazolin\u20105\u2010yl]benzene acetamide). Finally, ischemia\u2010induced injury and functional loss to the optic nerve was attenuated by blocking A<jats:sub>3<\/jats:sub> receptors. Together, these results indicate that adenosine may trigger oligodendrocyte death via activation of A<jats:sub>3<\/jats:sub> receptors and suggest that this mechanism contributes to optic nerve and white matter ischemic damage. 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