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. Author manuscript; available in PMC: 2015 Mar 1.
Published in final edited form as: Stroke. 2014 Jan 28;45(3):896–899. doi: 10.1161/STROKEAHA.113.004488

Figure 2.

Figure 2

A. Quantal Bioassays. Each bioassay describes the effect of low dose or high dose argatroban given at various delay time points, compared to saline8. The group tolerance to ischemia is characterized by the ED50, minutes of MCAo that renders 50% of the subjects abnormal. The ED50 of each treated group is compared to the saline group after a Bonferroni correction for multiple comparisons, illustrated with curves for those subjects treated after a 3-hour delay. Both low and high dose argatroban were significantly more protective than saline (p<0.05, t-test after Bonferroni). B. Sections after 48 hours with TTC staining. Representative sections from saline and argatroban treated subjects illustrating the pale, non-metabolizing area of lesioned cerebrum reduced by argatroban. Subjects received treatment 3 hours after onset of 2-hour MCAo, and were sacrificed 48 hours later. C. Lesion volume. Mean±SD total lesion volume is shown for each group at the relevant time delays. The volume of metabolic impairment is significantly reduced (improved) by low dose argatroban given immediately or after a 1-hour delay. ** p<0.01, ANOVA with Tukey's.