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. 2011 Sep;164(2b):681–693. doi: 10.1111/j.1476-5381.2011.01408.x

Figure 4.

Figure 4

Effect of i.pl. treatment with selective kinin B1 or B2 receptor antagonists, DALBK (3 nmol per paw, i.pl.) and Hoe 140 (3 nmol per paw, i.pl.), respectively, on paclitaxel-induced mechanical hyperalgesia in CD1 mice. A single injection of the drugs was given 7 (A) and 14 (B) days after the first paclitaxel (PTX) injection. (C) Effect of the i.pl. injection of kinin B1 or B2 receptor agonists, DABK (20 nmol per paw, i.pl.) and BK (10 nmol per paw, i.pl.), respectively, on licking behaviour in vehicle- and paclitaxel-treated CD1 mice. Each group represents the mean of five to six animals, and the error bars indicate the SEM. (A, B) *P < 0.05, significantly different from paclitaxel-treated mice (two-way anova followed by Bonferroni post-test). BL, baseline withdrawal threshold. (C) *P < 0.05, significantly different from saline- (i.pl.) injected mice (one-way anova followed by the Newman–Keuls post-test).