Y. Wada et al., COMPARISON OF THE EFFECTS OF VARIOUS ANTICHOLINERGIC DRUGS ON HUMAN ISOLATED URINARY-BLADDER, Archives internationales de pharmacodynamie et de therapie, 330(1), 1995, pp. 76-89
We investigated the effects of various anticholinergic drugs (atropine
, oxybutynin, terodiline and propiverine) on the contractions induced
by acetylcholine, KCl, CaCl2, and electrical field stimulation, in hum
an isolated urinary bladder smooth muscles using the muscle bath techn
ique. Urinary bladders wore obtained from 20 patients who underwent to
tal cystectomy due to malignant bladder tumor. The detrusor preparatio
ns were taken from the intact part of the dome of the bladder. Acetylc
holine caused a concentration-dependent contraction in human detrusor
preparations. Atropine (10(-9) - 10(-6) M), oxybutynin (10(-8) - 10(-5
) M). terodiline (10(-7) - 10(-5) M) and propiverine (10(-7) - 10(-5)
M) caused parallel shifts to the right of the concentration-response c
urves to acetylcholine. The rank order of pA(2) values was: atropine >
oxybutynin > terodiline = propiverine. Atropine did not suppress the
maximum contraction to acetylcholine, while the other drugs significan
tly suppressed the maximum contractions at the higher concentrations.
Each drug caused a concentration-dependent inhibition of the KCl (80 m
M)- and CaCl2 (5 mM)-induced contractions: the maximum inhibitions of
terodiline and propiverine were significantly greater than those of ox
ybutynin and atropine. Each drug caused a concentration-dependent inhi
bition of the contraction induced by electrical field stimulation; the
maximum inhibitions of terodiline and propiverine were significantly
greater than those of oxybutynin and atropine. The results suggest tha
t the drugs have both anticholinergic and calcium antagonistic effects
. Furthermore: it also appears that part of the human bladder contract
ion. which was significantly inhibited by terodiline and propiverine,
is an atropine-resistant component.