Sauviat M P, Garnier P, Goudey-Perriere F, Perriere C
Unité INSERM 275, Ecole Polytechnique-ENSTA, Palaiseau, France.
Toxicon. 1995 Sep;33(9):1207-13. doi: 10.1016/0041-0101(95)00049-r.
Venom isolated from the stonefish Synanceia verrucosa was assayed in concentrations of 0.07 and 5.7 micrograms/ml on frog atrial fibres and myocytes. Venom, less than 2.9 micrograms/ml, dose-dependently increased the amplitude and the duration of the stimulated peak tension, lengthened the time constant of the relaxation phase and shortened the duration of the action potential (AP). The concentration of venom 5.7 micrograms/ml decreased the amplitude of the peak tension, induced a contracture, reduced the amplitude of the plateau and shortened its duration as well as the repolarizing phase of the AP. The positive inotropic effect induced by the venom (2.9 micrograms/ml) on the contraction was inhibited dose-dependently by propranolol but was unchanged by the alpha-adrenergic antagonists urapidil and yohimbine, the adenyl cyclase activity remaining sensitive to forskolin. Venom, adrenalin and propranolol competed for a common site. Venom (2.9 micrograms/ml) increased both the Ca and the delayed outward K currents of enzymatically isolated atrial myocytes. The data suggest that the venom activates adrenoceptors, essentially beta-adrenoceptors.
从毒鲉(Synanceia verrucosa)中分离出的毒液,以0.07和5.7微克/毫升的浓度对蛙心房纤维和心肌细胞进行了检测。浓度低于2.9微克/毫升的毒液,剂量依赖性地增加了刺激峰值张力的幅度和持续时间,延长了舒张期的时间常数,并缩短了动作电位(AP)的持续时间。5.7微克/毫升的毒液浓度降低了峰值张力的幅度,诱发了挛缩,降低了平台期的幅度并缩短了其持续时间以及动作电位的复极化阶段。毒液(2.9微克/毫升)对收缩产生的正性肌力作用被普萘洛尔剂量依赖性地抑制,但α-肾上腺素能拮抗剂乌拉地尔和育亨宾对其无影响,腺苷酸环化酶活性对福斯高林仍保持敏感。毒液、肾上腺素和普萘洛尔竞争一个共同位点。毒液(2.9微克/毫升)增加了酶分离的心房肌细胞的钙电流和延迟外向钾电流。数据表明,毒液激活肾上腺素能受体,主要是β-肾上腺素能受体。