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

Figure 1.

Figure 1

Paclitaxel-induced hyperalgesia in kinin receptor-deficient mice. Mechanical (A) and thermal (B) withdrawal threshold of vehicle-treated wild-type (WT vehicle) mice, paclitaxel-treated WT (WT PTX) mice, paclitaxel-treated B1R−/−, (B1R−/− PTX) B2R−/− (B2R−/− PTX) and B1B2R−/− (B1B2R−/− PTX) mice were evaluated at different time intervals after the first paclitaxel treatment. (C, D) Inhibition of the AUC 0–6 h (from day 0 to 21) of paclitaxel-induced mechanical (C) and thermal (D) hyperalgesia in kinin receptor-deficient mice. The inhibition is shown as the AUC of the test group (receptor knock-out PTX animals), as a percentage of the control AUC (WT PTX animals). Each group represents the mean of five to six animals, and the error bars indicate the SEM. *P < 0.05 significantly different from paclitaxel-treated WT mice (two-way anova followed by the Bonferroni post-test). BL, baseline withdrawal threshold. #P < 0.05, significantly different from B1R−/− or B2R−/− group (one-way anova followed by the Newman–Keuls post-test).