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2006 merck/merial - School of Veterinary Medicine - Louisiana State ...

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and detrimental impacts on the brain after injury. Thus, it is important to follow the time course <strong>of</strong> CNS insults, such as thosecaused by stereotaxic techniques and ensuing glial activation. Expression <strong>of</strong> GFAP (glial fibrillary acidic protein), anastrocyte-specific marker, is activation dependent. Here, we have utilized a unique transgenic mouse model, FVB GFAP-luc,and bioluminescence imaging, to continuously monitor in vivo GFAP expression levels in the brains <strong>of</strong> mice that haveundergone stereotaxic manipulation. Mice were injected uni- or bilaterally with 6-OHDA or ascorbic acid (AA) control underanesthesia. Mice were imaged post-operatively for up to 21 days using Xenogen’s IVIS Bioluminescence Imaging set-up andLiving Image s<strong>of</strong>tware to monitor GFAP expression. At the end <strong>of</strong> live imaging, brains were dissected, ex vivo brain imageswere obtained, and brain tissues prepared for analyses. We have observed that (i) both AA and 6-OHDA markedly enhanceGFAP expression and (ii) the increased expression is greatest during the first week after injury, but is still present at 3 weeksafter injury. This data was confirmed with Western blot analysis for GFAP. Thus, it appears that (i) bioluminescenceimaging is a useful tool for monitoring glial response to injury and (ii) in these mice, astrocytic activation depends mostly onthe mechanical aspects <strong>of</strong> injury. Supported by ES11654 (NIH) and T35RR07071 (NIH).142

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