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通过诱导癌前谷胱甘肽S-转移酶P型阳性肝细胞灶证明致癌物的启动潜能:一种可能用于环境致癌物的体内检测系统。

Demonstration of initiation potential of carcinogens by induction of preneoplastic glutathione S-transferase P-form-positive liver cell foci: possible in vivo assay system for environmental carcinogens.

作者信息

Tsuda H, Matsumoto K, Ogino H, Ito M, Hirono I, Nagao M, Sato K, Cabral R, Bartsch H

机构信息

Second Department of Pathology, Fujita Health University School of Medicine, Aichi.

出版信息

Jpn J Cancer Res. 1993 Mar;84(3):230-6. doi: 10.1111/j.1349-7006.1993.tb02861.x.

DOI:10.1111/j.1349-7006.1993.tb02861.x
PMID:7683635
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5919141/
Abstract

In a development trial for an initiation bioassay system, 7 known carcinogens and 1 suspected carcinogen were examined. In experiment 1, group 1 animals were initially subjected to partial hepatectomy (PH) 12 h before administration of diethylnitrosamine, 2-amino-3-methylimidazo[4,5-f]-quinoline (IQ), captafol, alpha-hexachlorocyclohexane or diethylstilbestrol (DES), then 2 weeks later underwent a promotion procedure comprising administration of phenobarbital (0.05% in diet) for 8 weeks and D-galactosamine (300 mg/kg, i.g.) at week 3. Group 2 received the promotion protocol alone as in group 1. Initiating potential was assayed on the basis of significant increase in values of preneoplastic placental form glutathione S-transferase-positive (GST-P+) foci of more than 3 cells in cross section at week 10. Numbers and areas of GST-P+ foci in group 1 given IQ, captafol and DES were significantly increased as compared to group 2, confirming the validity of the protocol as an initiation assay. In Experiment 2, group 1 rats were subjected to PH and 12 h later received a suspected carcinogenic mixture of opium pyrolysate (OP) or carcinogenic pesticide p,p'-dichloro-diphenyltrichloroethane or hexachlorobenzene. Application of a modified promotion procedure comprising cholic acid (0.15%) and carbon tetrachloride (1 ml/kg, i.g.) revealed significant initiation potential for OP. Overall the results indicate that the current protocols may be useful for detection of the initiation potential of carcinogens irrespective of their mutagenicity.

摘要

在一项启动生物测定系统的开发试验中,对7种已知致癌物和1种疑似致癌物进行了检测。在实验1中,第1组动物在给予二乙基亚硝胺、2-氨基-3-甲基咪唑[4,5-f]喹啉(IQ)、克菌丹、α-六六六或己烯雌酚(DES)前12小时先进行部分肝切除术(PH),然后在2周后进行促癌程序,包括给予苯巴比妥(饮食中含0.05%)8周,并在第3周给予D-半乳糖胺(300mg/kg,腹腔注射)。第2组仅接受与第1组相同的促癌方案。根据第10周时横截面中超过3个细胞的癌前胎盘型谷胱甘肽S-转移酶阳性(GST-P+)灶的值显著增加来测定启动潜能。与第2组相比,给予IQ、克菌丹和DES的第1组中GST-P+灶的数量和面积显著增加,证实了该方案作为启动测定的有效性。在实验2中,第1组大鼠接受PH,12小时后给予鸦片裂解物(OP)的疑似致癌混合物或致癌农药对,对'-二氯二苯三氯乙烷或六氯苯。应用包含胆酸(0.15%)和四氯化碳(1ml/kg,腹腔注射)的改良促癌程序显示OP具有显著的启动潜能。总体而言,结果表明当前方案可能有助于检测致癌物的启动潜能,而不论其致突变性如何。

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