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Fig. 3 | Journal of Experimental & Clinical Cancer Research

Fig. 3

From: VEGF-A/VEGFR-1 signalling and chemotherapy-induced neuropathic pain: therapeutic potential of a novel anti-VEGFR-1 monoclonal antibody

Fig. 3

VEGF165b increases spontaneous and noxious-evoked activity of NS neurons through VEGFR-1. Representative ratematers showing spontaneous and noxious-evoked activity of NS neurons after spinal application of VEGF165b alone or in combination with D16F7 mAb (a and b, respectively); black arrows indicate the noxious stimulation on the mouse hind-paw. Mean ± SEM population data of spinal cord application of VEGF165b (3 ng/5 μl) in the presence of vehicle (0.9% NaCl), or D16F7 (100 pg/5 μl) on firing rate of spontaneous activity (c), frequency (d) and duration of evoked activity (e) of NS neurons in CD1 mice. Black arrows indicate vehicle, D16F7 or VEGF165b spinal application. Each point represents the mean of 5 different mice per group (one neuron recorded per each mouse). #P < 0.05, ##P < 0.01 and ###P < 0.001 indicate statistical difference vs baseline; *P < 0.05, **P < 0.01 and ***P < 0.001 indicate statistical difference vs vehicle + VEGF165b. One-way ANOVA followed by Dunnet’s multiple comparison post-hoc test was performed for statistical significance within groups. Two-way ANOVA followed by Bonferroni post-hoc test was used for comparison between groups

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