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N-亚硝基-2-乙酰氨基芴:一种在斯普拉格-道利大鼠中诱发肝细胞癌的直接致癌物。

N-nitroso-2-acetylaminofluorene: a direct-acting carcinogen inducing hepatocellular carcinoma in Sprague-Dawley rats.

作者信息

Ho Y S, Lin J K

机构信息

Institute of Biochemistry, College of Medicine, National Taiwan University, Taipei, Republic of China.

出版信息

Jpn J Cancer Res. 1994 Aug;85(8):794-800. doi: 10.1111/j.1349-7006.1994.tb02950.x.

Abstract

To compare the hepatotoxicity and hepatocarcinogenicity of N-nitroso-2-acetylaminofluorene (NO-AAF) and its parent compound, 2-acetylaminofluorene (AAF), male Sprague-Dawley rats were given intraperitoneal (i.p.) or subcutaneous (s.c.) injections of AAF or NO-AAF (60 mg/kg body weight/week) for ten months. In the AAF group, morphological changes were produced which involved gross distortions of the liver with multiple nodule formations. The rat livers in the NO-AAF group appeared to be smooth with a blunt-thick superior segment of the lateral lobe. The serum gamma-glutamyl transpeptidase activity in both the AAF group and the NO-AAF group was significantly elevated (P < 0.0005). The present study shows that i.p. and s.c. injections of NO-AAF resulted in a high incidence of well-differentiated hepatocellular carcinomas (HCC) (7/9 and 4/6, respectively), while poorly differentiated HCCs were induced by i.p. or s.c. administration of AAF (6/9 or 2/6, respectively). Subcutaneous lesions consisting of an inflammatory reaction and fibroadenoma formation were observed in the NO-AAF-treated rats, whereas no such skin lesions were detected in the AAF-treated animals. These results suggest that NO-AAF is a new direct-acting carcinogen which may be useful for investigating hepatocarcinogenesis.

摘要

为比较N-亚硝基-2-乙酰氨基芴(NO-AAF)及其母体化合物2-乙酰氨基芴(AAF)的肝毒性和肝癌致癌性,对雄性斯普拉格-道利大鼠进行腹腔内(i.p.)或皮下(s.c.)注射AAF或NO-AAF(60毫克/千克体重/周),持续十个月。在AAF组中,出现了形态学变化,包括肝脏严重变形并形成多个结节。NO-AAF组大鼠的肝脏外观光滑,外侧叶上半部分钝厚。AAF组和NO-AAF组的血清γ-谷氨酰转肽酶活性均显著升高(P < 0.0005)。本研究表明,腹腔内和皮下注射NO-AAF导致高分化肝细胞癌(HCC)的发生率较高(分别为7/9和4/6),而腹腔内或皮下注射AAF则诱导出低分化HCC(分别为6/9或2/6)。在接受NO-AAF治疗的大鼠中观察到由炎症反应和纤维腺瘤形成组成的皮下病变,而在接受AAF治疗的动物中未检测到此类皮肤病变。这些结果表明,NO-AAF是一种新的直接致癌物,可能有助于研究肝癌发生机制。

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