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. 2018 Apr 4;7(2):159–167. doi: 10.1016/j.imr.2018.03.006

Table 3.

Effect of trimethoxy flavones (TMF) on paclitaxel – induced thermal hyperalgesia in mice@

Dose of test compounds (mg/kg, s.c) Mean increase in reaction time (seconds)
7, 2′,3′ – TMF 7, 2′,4′ – TMF 7, 3′,4′ – TMF 7, 5, 4′ – TMF
25 1.83 ± 0.55 (8.87) 1.12 ± 0.31(5.31) 2.27 ± 0.41*(11.08) 1.04 ± 0.23(4.91)
50 5.62 ± 0.57* (27.88) 2.98 ± 0.37* (14.64) 3.64 ± 0.49* (17.95) 1.47 ± 0.37(7.07)
100 8.52 ± 0.56* (42.42) 5.69 ± 0.74* (28.23) 5.42 ± 0.91* (26.88) 3.97 ± 0.44*(19.60)
200 10.17 ± 1.09* (50.70) 7.80 ± 0.50* (38.81) 8.23 ± 0.84* (40.97) 5.86 ± 0.84*(29.08)

Each value represents the mean ± S.E.M of six observations.

The values in parenthesis indicate the percentage of maximal protective effect.

The mean increase in reaction time in vehicle treated animals was 0.06 ± 0.04 sec.

The mean increase in reaction time after morphine (10 mg/kg) treatment was 15.09 ± 0.88 sec* (75.37%).

*

P < 0.05 compared with vehicle treatment.

@

All treatment groups received paclitaxel (10 mg/kg, i.p.) 24 h prior to the test. Thermal hyperalgesia was determined before and 30 min after vehicle/morphine/TMF treatment on the next day. The mean increase in reaction time represents the difference in time latency recorded before and after treatment with the vehicle / test compounds.