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Assessment of the Mutagenic Activity of Extracts of Brazilian Propolis in Topical Pharmaceutical Formulations on Mammalian Cells In Vitro and In Vivo

机译:巴西蜂胶提取物在体外和体内局部药物制剂对哺乳动物细胞的致突变活性评估

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摘要

Propolis possesses various biological activities such as antibacterial, antifungal, anti-inflammatory, anesthetic and antioxidant properties. A topically applied product based on Brazilian green propolis was developed for the treatment of burns. For such substance to be used more safely in future clinical applications, the present study evaluated the mutagenic potential of topical formulations supplemented with green propolis extract (1.2, 2.4 and 3.6%) based on the analysis of chromosomal aberrations and of micronuclei. In the in vitro studies, 3-h pulse (G1 phase of the cell cycle) and continuous (20 h) treatments were performed. In the in vivo assessment, the animals were injured on the back and then submitted to acute (24 h), subacute (7 days) and subchronic (30 days) treatments consisting of daily dermal applications of gels containing different concentrations of propolis. Similar frequencies of chromosomal aberrations were observed for cultures submitted to 3-h pulse and continuous treatment with gels containing different propolis concentrations and cultures not submitted to any treatment. However, in the continuous treatment cultures treated with the 3.6% propolis gel presented significantly lower mitotic indices than the negative control. No statistically significant differences in the frequencies of micronuclei were observed between animals treated with gels containing different concentrations of propolis and the negative control for the three treatment times. Under the present conditions, topical formulations containing different concentrations of green propolis used for the treatment of burns showed no mutagenic effect in either test system, but 3.6% propolis gel was found to be cytotoxic in the in vitro test.
机译:蜂胶具有多种生物活性,例如抗菌,抗真菌,消炎,麻醉和抗氧化特性。开发了一种基于巴西绿色蜂胶的局部应用产品,用于治疗烧伤。为了使此类物质在未来的临床应用中更安全地使用,本研究基于对染色体畸变和微核的分析,评估了添加了绿色蜂胶提取物(1.2%,2.4%和3.6%)的局部制剂的诱变潜力。在体外研究中,进行了3​​ h脉冲(细胞周期的G1期)和连续(20 h)治疗。在体内评估中,将动物背部弄伤,然后进行急性治疗(24小时),亚急性(7天)和亚慢性(30天),包括每天经皮肤应用含有不同浓度蜂胶的凝胶。对于经受3小时脉冲的培养物以及用含有不同蜂胶浓度的凝胶连续处理的培养物和未进行任何处理的培养物进行连续处理,观察到了相似的染色体畸变频率。但是,在连续处理中,用3.6%蜂胶凝胶处理的培养物的有丝分裂指数明显低于阴性对照。在三个处理时间内,用含有不同浓度蜂胶的凝胶处理的动物与阴性对照之间在微核频率上没有观察到统计学上的显着差异。在当前条件下,用于治疗烧伤的含有不同浓度绿色蜂胶的局部制剂在任一测试系统中均未显示致突变作用,但在体外测试中发现3.6%的蜂胶凝胶具有细胞毒性。

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