Molinari J L, Tato Zaldivar P, Méndez L
Ann Immunol (Paris). 1979 Nov-Dec;130(6):859-77.
A protein fraction, which consisted of at least 12 proteins, was obtained from the venom of Mexican scorpion Centruroides limpidus limpidus. The molecular weights of these proteins ranged between 9,800 and 163,000 daltons. This fraction was separated from the rest of the venom components, which were almost all neurotoxins, by chromatographying the venom obtained by electrical stimulation through a Sephadex G-50M column. This fraction was non-toxic for mice, even at dose of 200 micrograms/mouse. The most important is that it was able to induce immunity against C. l. limpidus venom, since 92.8% of the animals inoculated with three doses survived after the challenge with 39.2 micrograms of venom (2 DL50 for mice of 20 g); on the contrary, 88 min after the challenge, 100% of the control mice had already died. In another experiment, this immunogen was inoculated into mice three times at variable doses. Seven days after the last injection, each mouse was challenged with 19.6 micrograms of venom. In all controls the typical envenomation picture produced by scorpion venom was developed, and death was registered in 19% of the animals. In contrast, 87% of mice immunized with the highest dose failed to show signs of envenomation or died throughout the observation time. Only two immunized animals (13%) showed mild tachycardia and hyperpnea at 120 min post-challenge. Immunoelectrophoresis and immunodiffusion tests revealed that these proteins induced antibodies against components of the most toxic fraction.
从墨西哥蝎毒蜥蝎(Centruroides limpidus limpidus)的毒液中获得了一种蛋白质组分,该组分至少由12种蛋白质组成。这些蛋白质的分子量在9800至163000道尔顿之间。通过将电刺激获取的毒液经葡聚糖凝胶G - 50M柱进行色谱分离,该组分与毒液的其他几乎全是神经毒素的成分分离开来。该组分对小鼠无毒,即使剂量为200微克/小鼠。最重要的是,它能够诱导针对毒蜥蝎毒液的免疫,因为用三剂接种的动物中,92.8%在用39.2微克毒液(20克小鼠的2倍半数致死量)攻击后存活;相反,攻击后88分钟,100%的对照小鼠已经死亡。在另一项实验中,以不同剂量将这种免疫原给小鼠接种三次。最后一次注射七天后,每只小鼠用19.6微克毒液攻击。在所有对照组中都出现了蝎毒产生的典型中毒症状,19%的动物死亡。相比之下,用最高剂量免疫的小鼠中,87%在整个观察期内未表现出中毒迹象或死亡。仅两只免疫动物(13%)在攻击后120分钟出现轻度心动过速和呼吸急促。免疫电泳和免疫扩散试验表明,这些蛋白质诱导产生了针对毒性最强组分成分的抗体。