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. Author manuscript; available in PMC: 2008 Jul 1.
Published in final edited form as: J Cereb Blood Flow Metab. 2007 Jan 10;27(7):1339–1351. doi: 10.1038/sj.jcbfm.9600440

Figure 6.

Figure 6

(A) Western blot showing the effects of pretreatment with SCH23390 or sulpiride on nitrotyrosine immunoreactivity on multiple protein bands in putamen of sham or hypoxia–ischemia (H–I) piglets at 3 h of recovery. In all, 20 μg of protein was loaded onto gels, and antibodies against 3-nitrotyrosine (1:40,000) were used to detect proteins with nitrotyrosine. Synaptophysin was used as a loading control. (B) Optical density was integrated over all protein band values (means± s.d.) and was normalized to the sham + saline value from four independent gels. *P < 0.05 versus sham groups treated with saline; #P < 0.05 versus H–I group treated with saline; one-way ANOVA followed by the Student–Newman–Keuls test.