In this study, we attemped to identify the interactions and mechanisms
between veratrine and paeoniflorin on isolated rat atria. Paeoniflori
n alone showed no effect on the rat atria. Veratrine increased the atr
ial contraction and induced arrhythmia at 1 x 10(-5) g/ml. Veratrine c
ould directly induce contraction and elicit tetanic contraction at 1 x
10(-4) g/ml in the left atria with or without electric stimulation. P
aeoniflorin (4.8 x 10(-6) to 4.8 x 10(-3) g/ml), verapamil (2.2 x 10(-
6) g/ml), tetrodotoxin (TTX) (3.2 x 10(-8) g/ml) and quinidine (7.5 x
10(-6) g/ml) inhibited the increase of contraction and delayed the ons
et of contraction induced by veratrine (1 x 10(-5) g/ml). The inhibito
ry effect of paeoniflorin combined with verapamil on the contraction i
nduced by veratrine was more potent than that of paeoniflorin or verap
amil alone, However, the inhibitory effect of paeoniflorin was not pot
entiated by TTX or quinidine. From the above results, the contraction
evoked by veratrine in the rat atria may be concluded to be caused by
the stimulation of Na+- and Ca2+-ion channels. The inhibition of paeon
iflorin on the contraction induced by veratrine may primarily be relat
ed to the blockade of Ca2+ channels. (C) 1997 Elsevier Science Ireland
Ltd.