Table 3.
Tactile allodynia (g) | ||||||
---|---|---|---|---|---|---|
0 min | 5 min | 10 min | 15 min | 30 min | 60 min | |
Control rats | ||||||
Vehicle | 9.7 ± 0.3 | 9.7 ± 0.3 | 9.3 ± 0.7 | 9.7 ± 0.3 | 9.7 ± 0.3 | 9.7 ± 0.3 |
DABK (9.6 nmol, i.t.) | 9.7 ± 0.3 | 9.7 ± 0.3 | 9.3 ± 0.7 | 9.7 ± 0.3 | 9.7 ± 0.3 | 9.7 ± 0.3 |
SSR240612 (10 μg, i.t.) + DABK | 10.7 ± 0.3 | 9.7 ± 0.3 | 9.3 ± 0.7 | 9.7 ± 0.3 | 9.7 ± 0.3 | 9.7 ± 1.3 |
FLU (1 nmol, i.t.) + DABK | 9.7 ± 0.3 | 9.7 ± 0.3 | 9.3 ± 0.7 | 9.7 ± 0.3 | 9.7 ± 0.3 | 9.7 ± 0.3 |
Mino (10 mg/kg, i.p.) + DABK | 9.7 ± 0.3 | 9.7 ± 0.3 | 9.3 ± 0.7 | 9.7 ± 0.3 | 9.7 ± 0.3 | 9.7 ± 0.3 |
Tactile allodynia (g) | ||||||
0 min | 5 min | 10 min | 15 min | 30 min | 60 min | |
STZ-treated rats | ||||||
Vehicle | 6.3 ± 0.3*** | 6.0 ± 0.5*** | 6.3 ± 0.3*** | 6.3 ± 0.3*** | 6.3 ± 0.3*** | 6.0 ± 0.5*** |
DABK (9.6 nmol, i.t.) | 6.0 ± 0.5*** | 5.3 ± 0.4*** | 4.3 ± 0.3++ *** | 5.3 ± 0.4*** | 6.0 ± 0.0*** | 5.7 ± 0.3*** |
SSR240612 (10 μg, i.t.) + DABK | 9.3 ± 0.3+++ | 9.3 ± 0.0+++ | 9.3 ± 0.0+++ | 9.3 ± 0.3+++ | 9.7 ± 0.3+++ | 9.3 ± 0.0+++ |
FLU (1 nmol, i.t.) + DABK | 9.7 ± 0.3+++ | 9.7 ± 0.3+++ | 9.7 ± 0.3+++ | 9.7 ± 0.3+++ | 9.3 ± 0.4+++ | 9.3 ± 0.4+++ |
Mino (10 mg/kg, i.p.) + DABK | 9.7 ± 0.3+++ | 9.0 ± 0.4+++ | 9.3 ± 0.4+++ | 9.3 ± 0.4+++ | 8.7 ± 0.4+++ | 9.3 ± 0.4+++ |
Time-course effect of a single intrathecal (i.t.) injection of the B1R agonist, des-Arg9-BK (DABK, 9.6 nmol), on the paw withdrawal threshold to tactile stimulation (g) in control and 4-day STZ-diabetic rats pre-treated, 3 h earlier, with either B1R antagonist (SSR240612), microglia inhibitors (minocycline, fluorocitrate) or vehicle. Data represent the mean ± S.E.M. of 4 to 12 rats in each group. Statistical comparison to vehicle in control (*) and STZ-treated rats (+) is indicated by ++P < 0.01; *** +++P < 0.001