Mello Clarissa P, Morais Isabel C O, Menezes Ramon R P P B, Pereira Gustavo J S, Torres Alba F C, Lima Dânya B, Pereira Ticiana P, Toyama Marcos H, Monteiro Helena S A, Smaili Soraya S, Martins Alice M C
Department of Clinical and Toxicological Analysis, Federal University of Ceará, Fortaleza 60430370, Ceará, Brazil.
Department of Physiology and Pharmacology, Faculty of Medicine, Federal University of Ceará, Fortaleza, Ceará, Brazil.
Toxicon. 2014 Sep;88:107-14. doi: 10.1016/j.toxicon.2014.05.009. Epub 2014 May 27.
Bothropoides insularis (jararaca-ilhoa) is a native endemic snake limited to the specific region of Queimada Island, on São Paulo coast. Several local and systemic effects have been described due to envenomation caused by it, such as edema, tissue necrosis, hemorrhage and acute renal failure. Our previous studies have shown that Bothropoides insularis venom (BinsV) demonstrated important functional and morphologic alterations in rat isolated kidney, especially decrease in tubular electrolyte transport, osmotic clearance and tubular necrosis. In order to elucidate the direct nephrotoxicity mechanism, the aim of the present study was to investigate BinsV cytotoxicity effect on renal epithelial cells. The treatment with BinsV over MDCK culture decreased cell viability in all concentrations tested with IC50 of 9 μg/mL. BinsV was able to induce membrane rupture and cell death with phosphatidilserine externalization. Furthermore, BinsV induced ROS overproduction and mitochondrial membrane potential collapse, as well as Bax translocation and caspases 3 and 7 expression. Therefore, these events might be responsible by BinsV-induced cell death caused by mitochondrial dysfunction and ROS overproduction in the direct cytotoxicity process.
海岛矛头蝮(jararaca-ilhoa)是一种本土特有蛇类,仅分布于圣保罗海岸的凯马达岛特定区域。它所导致的中毒会引发多种局部和全身效应,如水肿、组织坏死、出血以及急性肾衰竭。我们之前的研究表明,海岛矛头蝮蛇毒(BinsV)在大鼠离体肾脏中呈现出重要的功能和形态学改变,尤其是肾小管电解质转运、渗透清除率降低以及肾小管坏死。为了阐明直接肾毒性机制,本研究旨在探究BinsV对肾上皮细胞的细胞毒性作用。用BinsV处理MDCK培养物,在所有测试浓度下细胞活力均降低,IC50为9μg/mL。BinsV能够诱导细胞膜破裂和细胞死亡,并伴有磷脂酰丝氨酸外翻。此外,BinsV诱导活性氧(ROS)过量产生和线粒体膜电位崩溃,以及Bax易位和半胱天冬酶3和7表达。因此,这些事件可能是BinsV在直接细胞毒性过程中由线粒体功能障碍和ROS过量产生导致细胞死亡的原因。