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. Author manuscript; available in PMC: 2010 Apr 16.
Published in final edited form as: J Neuroimmune Pharmacol. 2009 Mar 3;4(2):249–259. doi: 10.1007/s11481-009-9148-4

Fig. 4.

Fig. 4

In vivo administration of O-1966 reduces endogenous leukocyte rolling and adhesion. C57BL/6 mice were immunized with MOG35–55. One group was treated with O-1966 (1 mg/kg) on days 7, 11, and 15. The control group received vehicle. Sham—non-immunized mice. Leukocyte rolling and adhesion to pial microvessels was measured on day 15 by intravital microscopy (cranial window) as previously described. *p<0.05, ***p<0.001 (Ni et al. 2004)