首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >An assessment of the genotoxicity of 2-hydroxy-1,4-naphthoquinone, the natural dye ingredient of Henna.
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An assessment of the genotoxicity of 2-hydroxy-1,4-naphthoquinone, the natural dye ingredient of Henna.

机译:指甲花天然染料成分2-羟基-1,4-萘醌的遗传毒性评估。

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摘要

2-Hydroxy-1,4-naphthoquinone (HNQ; Lawsone; CAS 83-72-7) is the principal natural dye ingredient contained in the leaves of Henna (Lawsonia inermis). Published genotoxicity studies on HNQ suggested it was a weak bacterial mutagen for Salmonella typhimurium strain TA98 or was more clearly mutagenic for strain TA 2637, both in the presence of metabolic activation. HNQ was unable to induce sex-linked recessive lethal mutations in Drosophila melanogaster. However, a small increase in micronucleus frequency was reported in the bone marrow of mice at a single mid-range dose level, 24h after intraperitoneal injection. In view of the wide use of Henna hair dyes it was deemed necessary to conduct a thorough investigation, under Good Laboratory Practice conditions, of the genotoxicity of HNQ. HNQ was non-mutagenic in bacterial (Ames test) or mammalian (V79 hprt) assays. It was borderline positive in a mouse lymphoma tk mutation assay and a chromosome aberration test (CHO cells), results that may reflect a similar clastogenic mechanism. Negative in vivo genotoxicity results were noted in the rat hepatocyte in vivo/in vitro UDS test, in peripheral lymphocytes (chromosome aberrations) of rats receiving repeated oral doses of HNQ at the MTD for 28 days, and in mouse and hamster bone marrow chromosome aberration tests. However small, but statistically significant increases in the incidence of bone marrow micronuclei were observed in two out of five tests at 72 h after dosing, but not at 24 or 48 h. There was evidence of haematotoxicity at 72 h, which may have been enhanced by the vehicle (DMSO) used in the positive tests. As erythropoiesis and administration of haematotoxic agents are known to induce small increases in the frequency of bone marrow micronuclei, typically at delayed sampling times, the data suggest that the positive 72 h response produced by HNQ is consistent with stimulation of haematopoiesis subsequent to haematological toxicity of HNQ, and not due to a DNA-reactive mechanism. Overall, the weight of evidence suggests that Henna and HNQ pose no genotoxic risk to the consumer.
机译:2-羟基-1,4-萘醌(HNQ; Lawsone; CAS 83-72-7)是指甲花(Lawsonia inermis)叶片中所含的主要天然染料成分。关于HNQ的已发表的遗传毒性研究表明,在存在代谢激活的情况下,它对于鼠伤寒沙门氏菌TA98菌株来说是一种弱细菌诱变剂,或者对于TA 2637菌株来说更明显地是诱变剂。 HNQ无法在果蝇中诱导与性相关的隐性致死突变。但是,腹膜内注射后24小时,在单个中剂量水平,小鼠骨髓中的微核频率有少量增加。鉴于指甲花染发剂的广泛使用,认为有必要在良好实验室规范条件下对HNQ的遗传毒性进行彻底研究。在细菌(Ames试验)或哺乳动物(V79 hprt)试验中,HNQ没有致突变性。在小鼠淋巴瘤tk突变试验和染色体畸变试验(CHO细胞)中,这是临界阳性,结果可能反映了类似的致分裂机制。在大鼠肝细胞体内/体外UDS测试,在MTD处重复口服HNQ达28天的大鼠的外周淋巴细胞(染色体畸变)以及在小鼠和仓鼠骨髓染色体畸变中,都发现了阴性的体内遗传毒性结果测试。然而,在给药后72小时,五分之二的测试中观察到骨髓微核的发生率有所提高,但有统计学上的显着性增加,而24小时或48小时则没有。有证据表明在72小时时有血液中毒,阳性试验中使用的媒介物(DMSO)可能会增强这种毒性。由于已知促红细胞生成和血液毒性药物的使用会引起骨髓微核频率的小幅增加,通常是在延迟的采样时间,因此数据表明,HNQ产生的阳性72 h反应与在对HNQ的血液学毒性后刺激造血作用相一致。 HNQ,而不是由于DNA反应机制。总体而言,有力的证据表明,指甲花和HNQ对消费者没有遗传毒性风险。

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