首页> 外文期刊>The Journal of toxicological sciences >In vitro and in vivo evaluation of mutagenicity of fucoxanthin (FX) and its metabolite fucoxanthinol (FXOH).
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In vitro and in vivo evaluation of mutagenicity of fucoxanthin (FX) and its metabolite fucoxanthinol (FXOH).

机译:岩藻黄质(FX)及其代谢产物岩藻黄质(FXOH)的致突变性的体外和体内评估。

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摘要

Mutagenicity of fucoxanthinol (FXOH), the major compound after oral ingestion of fucoxanthin (FX), was evaluated by in vitro Ames test, and of FX by in vivo micronucleus test. In in vitro Ames test, bacterial reverse mutation was examined by using Salmonella typhimurium strains TA98, TA100, TA1535 and TA1537, and Escherichia coli WP2uvrA/pKM101, with or without metabolic activation by S9 mix in the preincubation method, and mutagenicity of FXOH was found to be negative in all cases. In in vivo micronucleus test, mice were orally administered with FX at doses of 500, 1,000 and 2,000 mg/kg, and the bone marrow cells were taken 24 hr after the administration to observe the incidence of micronucleus cells, and mutagenicity of FX was found to be negative at all doses. Based on the data of the present study it can be presumed that orally administered FX is a safe compound in terms of mutagenicity under the experimental conditions employed here.
机译:通过体外Ames试验评估了口服口服岩藻黄质(FX)后的主要化合物岩藻黄质(FXOH)的致突变性,并通过体内微核试验评估了其致突变性。在体外Ames试验中,通过使用鼠伤寒沙门氏菌TA98,TA100,TA1535和TA1537以及大肠杆菌WP2uvrA / pKM101进行了细菌反向突变的检测,并在预温育方法中通过S9混合物进行了代谢激活或不进行代谢激活,并且发现了FXOH的致突变性在所有情况下均为负数。在体内微核试验中,以500、1,000和2,000 mg / kg的剂量给小鼠口服FX,给药后24小时取骨髓细胞观察微核细胞的发生,发现FX的致突变性在所有剂量下均为阴性。根据本研究的数据,可以认为口服FX在此处采用的实验条件下在致突变性方面是安全的。

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