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一种通过熟肉诱变剂鉴定遗传毒性风险的实验方法。

An experimental approach to identifying the genotoxic risk by cooked meat mutagens.

作者信息

Loprieno N, Boncristiani G, Loprieno G

机构信息

Dipartimento di Scienze dell'Ambiente e del Territorio dell'Università di Pisa, Italy.

出版信息

Adv Exp Med Biol. 1991;289:115-31. doi: 10.1007/978-1-4899-2626-5_9.

DOI:10.1007/978-1-4899-2626-5_9
PMID:1897387
Abstract

In order to define the toxicological risk for the human population derived from the chemical compounds formed during the process of cooking animal meat, which have been described to possess a mutagenic, genotoxic, and carcinogenic activity, an extensive study has been developed on cooked meat extract and two cooked meat mutagens, IQ and MeIQx. The study has been based on toxicokinetics and mouse tissue distribution of the two chemicals, on in vitro and in vivo mutagenicity/genotoxicity analyses (gene mutation, chromosome aberration, micronuclea in mouse bone marrow cells, mice urine and faeces mutagenicity test), as well as in vivo protein and DNA binding. The two chemicals have been found positive for the induction of gene mutation on Salmonella, but not in V-79 Chinese hamster cells; IQ only has been found positive for the induction of chromosome aberrations on CHO cells and cultured human lymphocytes. IQ and MeIQx were negative for the induction of micronuclea in mice treated with 40 mg/kg of the chemicals; the lowest effective administered dose to the mice which produced mutagenic urine was 0.4 mg/kg of IQ and 0.04 mg/kg of MeIQx. A dose of 40 mg/kg of IQ given by gavage to mice produced an excretion of 1-4% of the applied dose in the urine and 0.1-2% of the applied dose in the faeces, when evaluated chemically or mutagenically. The DNA adducts for the liver were correlated with the dose of the IQ and MeIQx administered to the mice. All the data have been used for defining a possible risk estimate derived to the human population as a consequence of a cooked meat diet.

摘要

为了确定人类因食用动物肉类烹饪过程中形成的具有致突变、基因毒性和致癌活性的化合物而面临的毒理学风险,针对熟肉提取物以及两种熟肉诱变剂IQ和MeIQx开展了一项广泛研究。该研究基于这两种化学物质的毒代动力学和在小鼠体内的组织分布、体外和体内的致突变性/基因毒性分析(基因突变、染色体畸变、小鼠骨髓细胞微核、小鼠尿液和粪便致突变性试验)以及体内蛋白质和DNA结合情况。已发现这两种化学物质对沙门氏菌有致基因突变作用呈阳性,但对V - 79中国仓鼠细胞则不然;仅IQ对CHO细胞和培养的人淋巴细胞的染色体畸变诱导呈阳性。对于用40毫克/千克这两种化学物质处理的小鼠,IQ和MeIQx对微核诱导呈阴性;对小鼠产生致突变尿液的最低有效给药剂量,IQ为0.4毫克/千克,MeIQx为0.04毫克/千克。当通过化学或致突变性评估时,给小鼠灌胃40毫克/千克的IQ,尿液中排出的给药剂量为1 - 4%,粪便中为0.1 - 2%。肝脏中的DNA加合物与给予小鼠的IQ和MeIQx剂量相关。所有这些数据都用于确定因食用熟肉饮食而可能给人类带来的风险估计。

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1
An experimental approach to identifying the genotoxic risk by cooked meat mutagens.一种通过熟肉诱变剂鉴定遗传毒性风险的实验方法。
Adv Exp Med Biol. 1991;289:115-31. doi: 10.1007/978-1-4899-2626-5_9.
2
An experimental approach to identifying the genotoxic risk from cooked meat mutagens.
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Mutagenic activation of IQ, PhIP and MeIQx by hepatic microsomes from rat, monkey and man: low mutagenic activation of MeIQx in cynomolgus monkeys in vitro reflects low DNA adduct levels in vivo.大鼠、猴和人肝脏微粒体对IQ、PhIP和MeIQx的诱变激活作用:食蟹猴体外实验中MeIQx的低诱变激活反映其体内低DNA加合物水平。
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Heterocyclic aromatic amines induce DNA strand breaks and cell transformation.杂环芳香胺会导致DNA链断裂和细胞转化。
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Cytochromes P450 in cynomolgus monkeys mutagenically activate 2-amino-3-methylimidazo[4,5-f]quinoline (IQ) but not 2-amino-3,8-dimethylimidazo[4,5-f]quinoxaline (MeIQx).食蟹猴体内的细胞色素P450可通过诱变激活2-氨基-3-甲基咪唑并[4,5-f]喹啉(IQ),但不能激活2-氨基-3,8-二甲基咪唑并[4,5-f]喹喔啉(MeIQx)。
Carcinogenesis. 1995 Jul;16(7):1549-55. doi: 10.1093/carcin/16.7.1549.
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In vivo mutagenicity and DNA adduct levels of heterocyclic amines in Muta mice and c-myc/lacZ double transgenic mice.Muta小鼠和c-myc/lacZ双转基因小鼠中杂环胺的体内诱变性和DNA加合物水平
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The synthesis and mutagenicity of the 3-ethyl analogues of the potent mutagens IQ, MeIQ, MeIQx and its 3,7-dimethyl isomer.强效诱变剂IQ、MeIQ、MeIQx及其3,7-二甲基异构体的3-乙基类似物的合成与致突变性。
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