Figure 5.
Figure 5. Effects of anti-P-selectin and anti-E-selectin mAbs on subacute (4-hour) Ang II-induced leukocyte responses within rat mesenteric postcapillary venules. Rats were treated intraperitoneally with saline (n = 6) or 1 nM Ang II (n = 6). In other groups of animals, 15 minutes before intraperitoneal administration of 1 nM Ang II, rats were treated with anti-P-selectin mAb (n = 5), anti-E-selectin mAb (n = 5), or a combination of both (n = 4). Four hours later, responses of leukocyte rolling flux (A), leukocyte rolling velocity (B), leukocyte adhesion (C), and leukocyte emigration (D) were quantified. Results are represented as mean ± SEM. **P < .01 relative to the saline group. ++P < .01 relative to the 1 nM Ang II group.

Effects of anti-P-selectin and anti-E-selectin mAbs on subacute (4-hour) Ang II-induced leukocyte responses within rat mesenteric postcapillary venules. Rats were treated intraperitoneally with saline (n = 6) or 1 nM Ang II (n = 6). In other groups of animals, 15 minutes before intraperitoneal administration of 1 nM Ang II, rats were treated with anti-P-selectin mAb (n = 5), anti-E-selectin mAb (n = 5), or a combination of both (n = 4). Four hours later, responses of leukocyte rolling flux (A), leukocyte rolling velocity (B), leukocyte adhesion (C), and leukocyte emigration (D) were quantified. Results are represented as mean ± SEM. **P < .01 relative to the saline group. ++P < .01 relative to the 1 nM Ang II group.

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