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首页> 外文期刊>Journal of biomedical materials research. Part B, Applied biomaterials. >Studies on the tumor-promoting activity of additives in biomaterials: inhibition of metabolic cooperation by phenolic antioxidants involved in rubber materials.
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Studies on the tumor-promoting activity of additives in biomaterials: inhibition of metabolic cooperation by phenolic antioxidants involved in rubber materials.

机译:添加剂在生物材料中的促肿瘤活性研究:通过参与橡胶材料的酚类抗氧化剂抑制代谢合作。

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For the detection of tumor-promoting activities of phenolic antioxidants, the inhibitory activities on the intercellular gap-junctional communication were investigated using the V79 metabolic cooperation (MC) assay. Among eight antioxidants, 4,4'-butylidene-bis(3-methyl-6-tert-butyl-phenol), 2,2'-methylene-bis(4-methyl-6-tert-butylphenol) (MBMBP), and styrenated phenol (SP) showed stronger inhibitory activities than lithocholic acid, which is known to be a tumor promotor. However, 4,4'-thio-bis(3-methyl-6-tert-butylphenol), Irganox 1010, and 1330 did not inhibit at any concentrations. When the single-electron oxidation potentials were compared among antioxidants, the electrochemical ease estimated with the first oxidation potential was correlated with the cytotoxic potentials (r = 0.88), but not with the inhibitory activities in an MC assay. The tumor-promoting activity of MBMBP was also investigated using an in vitro, two-stage Balb/c 3T3 transformation assay. MBMBP did not show initiating activity, but significant promoting activity at concentrations of both 1 and 2.5 micrograms/ml were noted. These concentrations were close to the lowest effective inhibitory concentration (1.3 micrograms/ml) of MBMBP in an MC assay. In conclusion, there is a possibility that the phenolic antioxidants that show inhibitory activities in an MC assay contribute to the enhancement of tumor incidence induced by biomaterials.
机译:为了检测酚类抗氧化剂的促肿瘤活性,使用V79代谢合作(MC)分析法研究了对细胞间间隙连接通讯的抑制活性。在八种抗氧化剂中,4,4'-亚丁基-双(3-甲基-6-叔丁基苯酚),2,2'-亚甲基-双(4-甲基-6-叔丁基苯酚)(MBMBP)和苯乙烯酚(SP)表现出比石胆酸强的抑制活性,后者已知是促进肿瘤的物质。但是,4,4'-硫代双(3-甲基-6-叔丁基苯酚),Irganox 1010和1330在任何浓度下均没有抑制作用。当在抗氧化剂中比较单电子氧化电位时,用第一个氧化电位估算的电化学难易程度与细胞毒性电位(r = 0.88)相关,但与MC分析中的抑制活性无关。还使用体外两阶段Balb / c 3T3转化试验研究了MBMBP的促肿瘤活性。 MBMBP没有显示启动活性,但是在1和2.5微克/ ml的浓度下都显示出显着的促进活性。这些浓度接近MC试验中MBMBP的最低有效抑制浓度(1.3微克/毫升)。总之,在MC分析中显示抑制活性的酚类抗氧化剂有可能有助于增强生物材料引起的肿瘤发生率。

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