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. Author manuscript; available in PMC: 2015 Jun 20.
Published in final edited form as: Neuroscience. 2014 Apr 24;271:1–8. doi: 10.1016/j.neuroscience.2014.04.025

Figure 1.

Figure 1

The typical evolution patterns of Ki, which detected BBB disruption at 1h, 72h and 144h after ischemic stroke, are demonstrated for a representative rat treated with tPA and AcSDKP (upper row) or tPA alone (lower row), respectively. The volume with elevated permeability values increased more slowly in the rat administered with tPA and AcSDKP than in the rat with tPA monotherapy.