Vasconcelos Flávio, Lanchote Vera Lúcia, Bendhack Lusiane M, Giglio José Roberto, Sampaio Suely Vilela, Arantes Eliane Candiani
Departamento de Física e Química, Faculdade de Ciências Farmacêuticas de Ribeirão Preto, USP, Av. do Café, s/n, 14040-903 Ribeirão Preto, SP, Brazil.
Comp Biochem Physiol C Toxicol Pharmacol. 2005 May;141(1):85-92. doi: 10.1016/j.cca.2005.05.012.
Scorpion toxins interact with ionic channels of excitable cells, leading to a massive release of neurotransmitters. Voltage-gated Na+ channel toxins are mainly responsible for the toxic effects of scorpion envenoming and can be classified into two classes: alpha- and beta-neurotoxins. TsTX-V and TsTX-I from Tityus serrulatus venom (TsV) are, respectively, examples of these toxins. In this work, we compared the effects of these toxins on mean arterial pressure (MAP) and catecholamines release in rats. Toxins were isolated by ion exchange chromatography (TsTX-I) followed by RP-HPLC (TsTX-V). All experiments were performed on conscious unrestrained rats previously catheterised. The toxins (15 and 30 microg/kg) and TsV (50 and 100 microg/kg) were injected intravenously. MAP was continuously monitored through femoral catheter. Epinephrine (E) and norepinephrine (NE) levels were determined by RP-HPLC with electrochemical detection, at 10 min before and 2.5, 30 and 90 min after treatments. Maximal pressor effects were observed at 2.5-3.5 min. TsV induced intense long lasting increase in MAP, as did TsTX-I. TsTX-V showed the lowest pressor effects. TsV showed the highest effects on catecholamines release, followed by TsTX-I and TsTX-V with maximal effect at 2.5 min, followed by a gradual reduction, however remaining higher than controls. Although both toxins act on Na+ channels, TsTX-I displayed significant and more intense effects on catecholamines release and blood pressure than TsTX-V. It seems that the toxicity of TsTX-V is not related only with its ability to release catecholamines, indicating that other neurotransmitters, may be involved in its toxicity.
蝎毒素与可兴奋细胞的离子通道相互作用,导致神经递质大量释放。电压门控钠通道毒素是蝎螫伤中毒性作用的主要原因,可分为两类:α-和β-神经毒素。来自锯齿钝尾蝎毒液(TsV)的TsTX-V和TsTX-I分别是这些毒素的例子。在这项工作中,我们比较了这些毒素对大鼠平均动脉压(MAP)和儿茶酚胺释放的影响。毒素通过离子交换色谱法(TsTX-I)分离,随后进行反相高效液相色谱法(TsTX-V)。所有实验均在先前已插管的清醒无拘束大鼠身上进行。毒素(15和30微克/千克)和TsV(50和100微克/千克)通过静脉注射。通过股动脉导管连续监测MAP。在治疗前10分钟以及治疗后2.5、30和90分钟,通过反相高效液相色谱法和电化学检测测定肾上腺素(E)和去甲肾上腺素(NE)水平。在2.5 - 3.5分钟观察到最大升压作用。TsV诱导MAP出现强烈且持久的升高,TsTX-I也是如此。TsTX-V显示出最低的升压作用。TsV对儿茶酚胺释放的影响最大,其次是TsTX-I和TsTX-V,在2.5分钟时达到最大效应,随后逐渐降低,但仍高于对照组。尽管两种毒素都作用于钠通道,但TsTX-I对儿茶酚胺释放和血压的影响比TsTX-V更显著且更强烈。似乎TsTX-V的毒性不仅与其释放儿茶酚胺的能力有关,这表明其他神经递质可能也参与了其毒性作用。