Xing Guoqiang, Zhang Hui, Liu Chunli, Guo Zhengyi, Yang Xiaoli, Wang Zhuo, Wang Bo, Lei Ying, Yang Rentan, Jiang Yufeng, Lv Hailong
Taian City Central Hospital, Taian, Shandong, China.
School of Medicine, Shihezi University, Shihezi, Xinjiang, China.
Exp Parasitol. 2019 May;200:55-60. doi: 10.1016/j.exppara.2019.02.008. Epub 2019 Feb 19.
This study aimed to observe the effects of sodium arsenite (NaAsO) on apoptosis of Echinococcus granulosus protoscoleces induced by albendazole (ABZ), and to explore the potential mechanism of NaAsO. According to the following final concentrations, the experimental groups were divided into 10 μM NaAsO, 20 μM NaAsO, 80 μM ABZ, 10 μM NaAsO+80 μM ABZ, and 20 μM NaAsO+80 μM ABZ. Viability was detected with 0.1% eosin staining. The ultrastructural alterations were visualized by scanning electron microscopy. Caspase-3 activity was assessed with colorimetric assay. Meanwhile, ELISA or WST were applied to detect the activities of antioxidases in NaAsO treatment groups. The maximum protoscolicidal effect was seen with the combination 20 μM NaAsO+80 μM ABZ. The ultrastructural damage detected after NaAsO+ABZ incubation were greater than those caused by ABZ alone and its primary damage site was the tegument of the parasite. The caspase-3 activity was clearly higher in protoscoleces treated with the combination of NaAsO+ABZ than when drugs were used separately. The activities of NQO-1, HO-1, GST, and SOD were significantly lower in protoscoleces incubated with NaAsO than the untreated controls (P < 0.05). According to our results, ABZ could induce protoscoleces apoptosis, and NaAsO could significantly augment sensitivity of protoscoleces to ABZ.
本研究旨在观察亚砷酸钠(NaAsO)对阿苯达唑(ABZ)诱导的细粒棘球绦虫原头节凋亡的影响,并探讨NaAsO的潜在作用机制。根据以下终浓度,将实验组分为10μM NaAsO、20μM NaAsO、80μM ABZ、10μM NaAsO + 80μM ABZ和20μM NaAsO + 80μM ABZ。用0.1%伊红染色检测活力。通过扫描电子显微镜观察超微结构变化。用比色法评估半胱天冬酶-3活性。同时,采用ELISA或WST检测NaAsO处理组中抗氧化酶的活性。20μM NaAsO + 80μM ABZ联合用药时原头节杀灭效果最佳。NaAsO + ABZ孵育后检测到的超微结构损伤大于单独使用ABZ所致,其主要损伤部位是寄生虫的体表。NaAsO与ABZ联合处理的原头节中半胱天冬酶-3活性明显高于单独用药时。与未处理的对照组相比,用NaAsO孵育的原头节中NQO-1、HO-1、GST和SOD的活性显著降低(P < 0.05)。根据我们的结果,ABZ可诱导原头节凋亡,而NaAsO可显著增强原头节对ABZ的敏感性。