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在中期大鼠肝脏生物测定中,7-甲氧基-2-硝基萘并[2,1-b]呋喃(R7000)缺乏促进活性。

Lack of promoting activity of 7-methoxy-2-nitro-naphtho-[2,1-b]furan (R7000) in a medium-term rat liver bioassay.

作者信息

Cui L, Hasegawa R, Zajdela F, Puapairoj P, Shirai T, Ito N

机构信息

First Department of Pathology, Nagoya City University Medical School, Japan.

出版信息

Cancer Lett. 1994 Jan 30;76(2-3):161-6. doi: 10.1016/0304-3835(94)90393-x.

DOI:10.1016/0304-3835(94)90393-x
PMID:8149345
Abstract

Among the nitro-naphthofurans, 7-methoxy-2-nitro-naphtho[2,1-b]furan (R7000) has proved to be a very potent mutagen that causes sarcomas at the subcutaneous injection site and carcinomas in the forestomach after p.o. administration. In the present study, possible promoting activity for diethylnitrosamine (200 mg/kg, i.p.)-initiated liver carcinogenesis was assessed in rats. R7000 dissolved in 5% ethanol solution at doses of 10 or 50 mg/l given as the drinking water for 6 weeks did not enhance development of pre-neoplastic glutathione S-transferase placental form positive foci. Thus, it was concluded that R7000 may not be carcinogenic for the rat liver under the present experimental conditions.

摘要

在硝基萘并呋喃类化合物中,7-甲氧基-2-硝基萘并[2,1-b]呋喃(R7000)已被证明是一种非常强效的诱变剂,皮下注射该物质会导致注射部位出现肉瘤,口服给药后会导致前胃出现癌。在本研究中,评估了R7000对经腹腔注射给予200 mg/kg二乙基亚硝胺引发的大鼠肝癌发生的潜在促进活性。将R7000溶解于5%乙醇溶液中,以10或50 mg/l的剂量作为饮用水给予大鼠6周,结果发现其并未增强癌前谷胱甘肽S-转移酶胎盘型阳性病灶的发展。因此,得出结论,在当前实验条件下,R7000可能对大鼠肝脏无致癌性。

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