Garnier P, Sauviat M P, Goudey-Perriere F, Perriere C
Laboratoire de Biologie Animale, Faculté de Pharmacie Université de Paris Sud, France.
Toxicon. 1997 Jan;35(1):47-55. doi: 10.1016/s0041-0101(96)00075-x.
Freshly purified but unstable verrucotoxin (VTX) and a more stable proteic complex of the toxin (p-VTX) were isolated from the venom of the stonefish Synanceia verrucosa and applied to frog atrial fibres. VTX and p-VTX decreased the amplitude and the duration of the stimulated peak tension and accelerated the relaxation phase of the contraction. The negative inotropic effect of p-VTX decreased with increasing the external Ca concentration ([Ca]o) in the Ringer solution. The negative chronotropic effect induced by p-VTX was insensitive to change in [Ca]o. It is reversed by glibenclamide. p-VTX shortened the duration of the plateau and the repolarizing phase of the action potential. Glibenclamide but not tetraethylammonium reversed the p-VTX-induced shortening of the AP repolarizing phase. The data suggest that the toxin isolated from the venom of S. verrucosa inhibits Ca channels and might activate ATP-sensitive potassium channels in frog atrial heart muscle.
从毒鲉(Synanceia verrucosa)的毒液中分离出新鲜纯化但不稳定的疣毒素(VTX)和一种更稳定的毒素蛋白复合物(p-VTX),并将其应用于蛙心房纤维。VTX和p-VTX降低了刺激峰值张力的幅度和持续时间,并加速了收缩的舒张期。p-VTX的负性肌力作用随着林格溶液中细胞外钙浓度([Ca]o)的增加而降低。p-VTX诱导的负性变时作用对[Ca]o的变化不敏感。它可被格列本脲逆转。p-VTX缩短了动作电位的平台期和复极化期的持续时间。格列本脲而非四乙铵可逆转p-VTX诱导的动作电位复极化期缩短。数据表明,从毒鲉毒液中分离出的毒素抑制钙通道,并可能激活蛙心房心肌中的ATP敏感性钾通道。