Figures & data
Figure 1. Chromatographic profile of the lyophilized aqueous extract obtained from C. icaco leaves (AEC). Conditions for elution: mobile phase methanol–water (5–100%), 1 h, C18 analytical column (25 cm × 0.46 mm, 5 μm), detection at 330 nm DAD-UV-Vis, 1 mL/min.
![Figure 1. Chromatographic profile of the lyophilized aqueous extract obtained from C. icaco leaves (AEC). Conditions for elution: mobile phase methanol–water (5–100%), 1 h, C18 analytical column (25 cm × 0.46 mm, 5 μm), detection at 330 nm DAD-UV-Vis, 1 mL/min.](/cms/asset/e7296665-e4c1-4e3c-826f-166af4b07092/iphb_a_1204618_f0001_c.jpg)
Figure 3. Time–response curve for the anti-nociceptive effect of the lyophilized aqueous extract obtained from C. icaco leaves (AEC; 400 mg/kg, p.o.) on acetic acid-induced writhing response in mice. Writhings were counted over 15 min following i.p. injection of acetic acid (0.8%). AEC (400 mg/kg, p.o.) was administered p.o. 0.5, 1, 2, 4, 8 or 24 h before acid acetic injection (0.8%). Control animals received an injection of vehicle by p.o. route. Each column represents mean ± SEM (n = 8, per group). *p < 0.05 versus control (ANOVA followed by Tukey’s test).
![Figure 3. Time–response curve for the anti-nociceptive effect of the lyophilized aqueous extract obtained from C. icaco leaves (AEC; 400 mg/kg, p.o.) on acetic acid-induced writhing response in mice. Writhings were counted over 15 min following i.p. injection of acetic acid (0.8%). AEC (400 mg/kg, p.o.) was administered p.o. 0.5, 1, 2, 4, 8 or 24 h before acid acetic injection (0.8%). Control animals received an injection of vehicle by p.o. route. Each column represents mean ± SEM (n = 8, per group). *p < 0.05 versus control (ANOVA followed by Tukey’s test).](/cms/asset/0bc92d55-104f-408e-95fb-6f03c58f8d9f/iphb_a_1204618_f0003_b.jpg)
Table 1. Effect of the lyophilized aqueous extract obtained from C. icaco leaves (AEC) or indomethacin (INDO), reference drug, on writhing induced by acetic acid- and formalin-induced nociceptive behaviour in mice.
Figure 4. Effect of acute administration of vehicle, lyophilized aqueous extract obtained from C. icaco leaves (AEC; 100, 200 or 400 mg/kg, p.o.) or morphine (MOR, 5 mg/kg, i.p.) on hot plate test in mice. The bars shown the latency time to animals express pain behaviour, so each column represents the mean ± SEM (n = 8, per group). *p < 0.001 versus control (ANOVA followed by Tukey’s test).
![Figure 4. Effect of acute administration of vehicle, lyophilized aqueous extract obtained from C. icaco leaves (AEC; 100, 200 or 400 mg/kg, p.o.) or morphine (MOR, 5 mg/kg, i.p.) on hot plate test in mice. The bars shown the latency time to animals express pain behaviour, so each column represents the mean ± SEM (n = 8, per group). *p < 0.001 versus control (ANOVA followed by Tukey’s test).](/cms/asset/d2477ed3-6341-4bc1-b933-b50a01aa0976/iphb_a_1204618_f0004_b.jpg)
Figure 5. Effect of acute administration of vehicle, lyophilized aqueous extract obtained from C. icaco leaves (AEC; 100, 200 or 400 mg/kg, p.o.) or indomethacin (IND, 10 mg/kg) on mechanical hyperalgesia induced by CG (300 μg/paw) (A) or TNF-α (100 pg/paw) (B). Each point represents the mean ± SEM of the variation of paw withdrawal threshold (in grams) to tactile stimulation of the ipsilateral hind paw. **p < 0.05 and ***p < 0.01, compared with vehicle-treated group (two-way ANOVA followed by Tukey’s test).
![Figure 5. Effect of acute administration of vehicle, lyophilized aqueous extract obtained from C. icaco leaves (AEC; 100, 200 or 400 mg/kg, p.o.) or indomethacin (IND, 10 mg/kg) on mechanical hyperalgesia induced by CG (300 μg/paw) (A) or TNF-α (100 pg/paw) (B). Each point represents the mean ± SEM of the variation of paw withdrawal threshold (in grams) to tactile stimulation of the ipsilateral hind paw. **p < 0.05 and ***p < 0.01, compared with vehicle-treated group (two-way ANOVA followed by Tukey’s test).](/cms/asset/3e5a9d97-fe87-4f6a-82db-7243c7ff6d34/iphb_a_1204618_f0005_b.jpg)
Figure 6. Effect of acute administration of vehicle, lyophilized aqueous extract obtained from C. icaco leaves (AEC; 100, 200 or 400 mg/kg, p.o.) or diazepam (DZP, 3 mg/kg, i.p.) on rota-rod test (A) or grip strength meter (B) in mice. ***p < 0.01, compared with vehicle-treated group (one-way ANOVA followed by Tukey’s test).
![Figure 6. Effect of acute administration of vehicle, lyophilized aqueous extract obtained from C. icaco leaves (AEC; 100, 200 or 400 mg/kg, p.o.) or diazepam (DZP, 3 mg/kg, i.p.) on rota-rod test (A) or grip strength meter (B) in mice. ***p < 0.01, compared with vehicle-treated group (one-way ANOVA followed by Tukey’s test).](/cms/asset/dd29e867-999e-4265-aca8-cc07173303aa/iphb_a_1204618_f0006_b.jpg)