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. Author manuscript; available in PMC: 2011 Oct 1.

Published in final edited form as: Exp Neurol. 2010 Jul 27;225(2):423–429. doi: 10.1016/j.expneurol.2010.07.020

Fig. 4 — Levels of oxidative damage to lipids and proteins are increased in PMs from brains of 3xTgAD mice compared with control mice. PM fractions isolated from the indicated brain regions were used to measure levels of isoprostanes (A), protein carbonyls (B) and nitrotyrosine (C). Values are the mean and SEM; n=6, by using pooled tissue from three mice per group. *p<0.01 compared with the value for WT. CTX, cerebral cortex; HIP, hippocampus; STR, striatum; CER, cerebellum; BS, brainstem.

Fig. 4 — Levels of oxidative damage to lipids and proteins are increased in PMs from brains of 3xTgAD mice compared with control mice. PM fractions isolated from the indicated brain regions were used to measure levels of isoprostanes (A), protein carbonyls (B) and nitrotyrosine (C). Values are the mean and SEM; n=6, by using pooled tissue from three mice per group. *p<0.01 compared with the value for WT. CTX, cerebral cortex; HIP, hippocampus; STR, striatum; CER, cerebellum; BS, brainstem.

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