Table 1.
VT, ml | CA, cmH2O | CD, min | RV, ml | VE, % | |
---|---|---|---|---|---|
Vehicle (n = 18) | 0.73 ± 0.14 | 32.92 ± 6.38 | 0.40 ± 0.10 | 0.17 ± 0.05 | 71.6 ± 12.9 |
Agonist (8-OH-DPAT; 0.3 mg/kg) | 0.52 ± 0.13* | 26.66 ± 4.89* | 0.47 ± 0.11 | 0.06 ± 0.03 | 86.1 ± 10.6 |
Antagonist (WAY-100635; 0.1 mg/kg) | 1.55 ± 0.36*† | 36.74 ± 6.47† | 0.36 ± 0.10† | 1.05 ± 0.31*† | 29.3 ± 22.9*† |
Values are means ± SE. 8-OH-DPAT, 8-hydroxy-2-(di-n-propylamino)-tetralin; CMGs, cystometrograms; VT, volume threshold; CA, contraction amplitude; CD, contraction duration; RV, residual volume; VE, voiding efficiency = VT − RV/VT;
P < 0.05 indicates a statistically significant difference compared with vehicle treatment (post hoc least significance difference test).
P < 0.05 indicates a statistically significant difference compared with 8-OH-DPAT treatment (post hoc least significance difference test).