Figure 5
Figure 5. Effect of tPA on locomotor activity and cerebral edema following MCAO. (A) Mean locomotor activity at 6, 24, and 48 hours after MCAO in wild-type (○) or tPA−/− mice (▪ and ▴); tPA−/− mice treated with murine tPA immediately after MCAO (▴). Error bars describe standard error of the mean; n = 6; *P < .05 when tPA−/− mice are compared with wild-type mice or with tPA−/− animals treated with tPA. (B) Evans blue dye extravasation in the same group of animals as panel A 48 hours after MCAO. Error bars describe standard error of the mean. *P < .01 when tPA−/− mice are compared with wild-type animals; †P < .05 when tPA−/− mice treated with recombinant tPA are compared with untreated tPA−/− mice. The pictures correspond to one representative brain in each experimental group. The blue staining is apparent in areas with increase in blood-brain barrier permeability (arrows).

Effect of tPA on locomotor activity and cerebral edema following MCAO. (A) Mean locomotor activity at 6, 24, and 48 hours after MCAO in wild-type (○) or tPA−/− mice (▪ and ▴); tPA−/− mice treated with murine tPA immediately after MCAO (▴). Error bars describe standard error of the mean; n = 6; *P < .05 when tPA−/− mice are compared with wild-type mice or with tPA−/− animals treated with tPA. (B) Evans blue dye extravasation in the same group of animals as panel A 48 hours after MCAO. Error bars describe standard error of the mean. *P < .01 when tPA−/− mice are compared with wild-type animals; †P < .05 when tPA−/− mice treated with recombinant tPA are compared with untreated tPA−/− mice. The pictures correspond to one representative brain in each experimental group. The blue staining is apparent in areas with increase in blood-brain barrier permeability (arrows).

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