Figure 4From: The Interleukin-8 (IL-8/CXCL8) Receptor Inhibitor Reparixin Improves Neurological Deficits and Reduces Long-term Inflammation in Permanent and Transient Cerebral Ischemia in RatsEffect of reparixin treatment under different schedules on neurological deficits after transient MCAO. Transient (1.5 h) MCAO was performed. Reparixin was administered as follows: Panels A–C: 15 mg/kg, i.v. 2 h after reperfusion (i.e. 3.5 h after MCAO) followed by two 15 mg/kg s.c. doses at 2 h intervals, then 3 times/day on days 2 and 3. Panels D–F: 15 mg/kg, i.v. 2 h after reperfusion (i.e. 3.5 h after MCAO) followed by s.c. infusion for 48 h at a rate of 10mg/h/kg. Panels G–I: 15 mg/kg, i.v. 4.5 h after reperfusion (6 h after MCAO) followed by s.c. infusion for 48 h at a rate of 10mg/h/kg. Neurological deficits were evaluated by De Ryck’s (left panels), Bederson’s (middle panels) and foot-fault (right panels) tests starting from 24 h after MCAO. Open circles, vehicle; closed circles, reparixin. For comparison, the scores of non-ischemic, sham-operated rats, i.e. “normal” values, are also shown as a thin line (normal values were: 16 for the De Ryck’s test, 5 for the Bederson’s test and 1–4 for the foot-fault test. Data are mean ± S.E. of 6–7. Statistical differences (Mann-Whitney): *P < 0.05 and **P < 0.01 vs. saline.Back to article page