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首页> 外文期刊>Integrative cancer therapies. >Simultaneous Assessment of the Efficacy and Toxicity of Marine Mollusc–Derived Brominated Indoles in an In Vivo Model for Early Stage Colon Cancer
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Simultaneous Assessment of the Efficacy and Toxicity of Marine Mollusc–Derived Brominated Indoles in an In Vivo Model for Early Stage Colon Cancer

机译:在早期结肠癌的体内模型中同时评估海洋软体动物衍生的溴化吲哚的功效和毒性。

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The acute apoptotic response to genotoxic carcinogens animal model has been extensively used to assess the ability of drugs and natural products like dietary components to promote apoptosis in the colon and protect against colorectal cancer (CRC). This work aimed to use this model to identify the main chemopreventative agent in extracts from an Australian mollusc Dicathais orbita, while simultaneously providing information on their potential in vivo toxicity. After 2 weeks of daily oral gavage with bioactive extracts and purified brominated indoles, mice were injected with the chemical carcinogen azoxymethane (AOM; 10 mg/kg) and then killed 6 hours later. Efficacy was evaluated using immunohistochemical and hematoxylin staining, and toxicity was assessed via hematology, blood biochemistry, and liver histopathology. Comparison of saline- and AOM-injected controls revealed that potential toxic side effects can be interpreted from blood biochemistry and hematology using this short-term model, although AOM negatively affected the ability to detect histopathological effects in the liver. Purified 6-bromoisatin was identified as the main cancer preventive agent in the Muricidae extract, significantly enhancing apoptosis and reducing cell proliferation in the colonic crypts at 0.05 mg/g. There was no evidence of liver toxicity associated with 6-bromoisatin, whereas 0.1 mg/g of the brominated indole tyrindoleninone led to elevated aspartate aminotransferase levels and a reduction in red blood cells. As tyrindoleninone is converted to 6-bromoisatin by oxidation, this information will assist in the optimization and quality control of a chemopreventative nutraceutical from Muricidae. In conclusion, preliminary data on in vivo safety can be simultaneously collected when testing the efficacy of new natural products, such as 6-bromoisatin from Muricidae molluscs for early stage prevention of colon cancer.
机译:对遗传毒性致癌物动物模型的急性凋亡反应已广泛用于评估药物和天然产物(如饮食成分)在结肠中促进细胞凋亡并预防结直肠癌(CRC)的能力。这项工作旨在使用这种模型来鉴定澳大利亚软体动物双足纲的提取物中的主要化学预防剂,同时提供有关其潜在的体内毒性的信息。每天用生物活性提取物和纯化的溴化吲哚进行管饲2周后,给小鼠注射化学致癌物质z氧基甲烷(AOM; 10 mg / kg),然后在6小时后杀死。使用免疫组织化学和苏木精染色评估疗效,并通过血液学,血液生化和肝组织病理学评估毒性。盐水注射和AOM注射的对照的比较显示,尽管AOM对检测肝脏组织病理学影响产生了负面影响,但使用这种短期模型可以从血液生化和血液学方面解释潜在的毒副作用。纯化的6-溴异丁香素被鉴定为Muricidae提取物中的主要癌症预防剂,以0.05 mg / g的浓度显着增强结肠隐窝的凋亡并减少细胞增殖。没有证据表明6-溴异丁香素具有肝毒性,而0.1 mg / g的溴化吲哚酪氨酸多烯酮导致升高的天冬氨酸转氨酶水平和红细胞减少。由于酪蛋白烯酮可以通过氧化转化为6-溴异丁香素,因此该信息将有助于对鼠科的化学预防性保健食品进行优化和质量控制。总之,在测试新型天然产物(例如鼠科软体动物的6-溴异丁香素)对结肠癌的早期预防的功效时,可以同时收集体内安全性的初步数据。

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