PT - JOURNAL ARTICLE AU - Shan Zhu AU - Mingwei Li AU - Bryan E. Figueroa AU - Aijian Liu AU - Irina G. Stavrovskaya AU - Piera Pasinelli AU - M. Flint Beal AU - Robert H. Brown, Jr AU - Bruce S. Kristal AU - Robert J. Ferrante AU - Robert M. Friedlander TI - Prophylactic Creatine Administration Mediates Neuroprotection in Cerebral Ischemia in Mice AID - 10.1523/JNEUROSCI.1278-04.2004 DP - 2004 Jun 30 TA - The Journal of Neuroscience PG - 5909--5912 VI - 24 IP - 26 4099 - http://www.jneurosci.org/content/24/26/5909.short 4100 - http://www.jneurosci.org/content/24/26/5909.full SO - J. Neurosci.2004 Jun 30; 24 AB - Creatine mediates remarkable neuroprotection in experimental models of amyotrophic lateral sclerosis, Huntington's disease, Parkinson's disease, and traumatic brain injury. Because caspase-mediated pathways are shared functional mechanistic components in these diseases, as well as in ischemia, we evaluated the effect of creatine supplementation on an experimental stroke model. Oral creatine administration resulted in a remarkable reduction in ischemic brain infarction and neuroprotection after cerebral ischemia in mice. Postischemic caspase-3 activation and cytochrome c release were significantly reduced in creatine-treated mice. Creatine administration buffered ischemia-mediated cerebral ATP depletion. These data provide the first direct correlation between the preservation of bioenergetic cellular status and the inhibition of activation of caspase cell-death pathways in vivo. An alternative explanation to our findings is that creatine is neuroprotective through other mechanisms that are independent of mitochondrial cell-death pathways, and therefore postischemic ATP preservation is the result of tissue spearing. Given its safety record, creatine might be considered as a novel therapeutic agent for inhibition of ischemic brain injury in humans. Prophylactic creatine supplementation, similar to what is recommended for an agent such as aspirin, may be considered for patients in high stroke-risk categories.