Yurdakok Begum, Kismali Gorkem, Ozen Dogukan
Department of Pharmacology and Toxicology, Ankara University Faculty of Veterinary Medicine, Ankara 06110, Turkey.
Department of Biochemistry, Ankara University Faculty of Veterinary Medicine, Ankara 06110, Turkey.
Oncol Lett. 2014 Oct;8(4):1839-1843. doi: 10.3892/ol.2014.2378. Epub 2014 Jul 24.
Ptaquiloside (PTA) is a potent genotoxic carcinogenic compound, which is found in bracken ferns and predominantly causes gastric tumors in humans, as well as bladder tumors and chronic enzootic hematuria in cattle. The underlying molecular mechanisms of PTA remain a topic for interdisciplinary investigation. The aim of the present study was to determine the possible cytotoxic effect of 24 h of PTA exposure in Crandall feline kidney (CrFK) and human gastric cells (the HGC-27 cell line) using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay and lactose dehydrogenase (LDH) analysis. The cytotoxic effects of PTA (0.0005-500 μg/ml) were found to increase in a dose-dependent manner, whereby the half maximal inhibitory concentration values were 11.17 and 11.86 μg/ml in the CrFK cells, and 2.03 and 2.56 μg/ml in the HGC-27 cells, by LDH and MTT assay, respectively. The results of the present study are consistent with those of previous studies associated with the cytotoxicity of PTA; however, cytotoxicity was identified to occur at significantly lower doses. This cytotoxic effect at particularly high doses may be linked to the initiation of carcinogenesis as a result of oxidative stress.
ptaquiloside(pta)是一种具有潜在遗传毒性的致癌化合物,存在于蕨类植物中,主要导致人类患胃癌,以及牛患膀胱癌和慢性地方流行性血尿症。pta的潜在分子机制仍是一个跨学科研究的课题。本研究的目的是使用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)法和乳酸脱氢酶(LDH)分析,确定pta暴露24小时对克兰德尔猫肾(CrFK)细胞和人胃细胞(HGC-27细胞系)可能产生的细胞毒性作用。通过LDH和MTT分析发现,pta(0.0005-500μg/ml)的细胞毒性作用呈剂量依赖性增加,在CrFK细胞中,半数最大抑制浓度值分别为11.17和11.86μg/ml,在HGC-27细胞中分别为2.03和2.56μg/ml。本研究结果与先前关于pta细胞毒性的研究结果一致;然而,已确定细胞毒性在显著更低的剂量下就会发生。这种在特别高剂量下的细胞毒性作用可能与氧化应激导致的致癌作用起始有关。