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亚硝酸钠对2-乙酰氨基芴诱导大鼠肝癌发生过程中核原癌基因表达的潜在影响。

Potential effect of sodium nitrite on the expression of nuclear proto-oncogenes during 2-acetyl aminofluorene-induced hepatocarcinogenesis in rats.

作者信息

Hsu J D, Hsu C L, Chou F P, Wen P H, Wang C J

机构信息

Department of Pathology, Chung Shan Medical and Dental College, Hospital, Tauchung, Taiwan, People's Republic of China.

出版信息

Chem Biol Interact. 1997 Dec 12;108(1-2):1-18. doi: 10.1016/s0009-2797(97)00089-6.

Abstract

2-acetyl aminofluorene (AAF) reacts in acidic conditions with nitrous fume yielding N-nitroso-AAF (N-NO-AAF), as previously described, that exerts more toxic and mutagenic effects than its parental compound. In this study, the effect of sodium nitrite (NaNO2) on the tumorigenicity of AAF in rats fed with AAF and NaNO2 was observed. Wistar rats were divided into five groups: group I served as control; group II were treated with NaNO2 (0.3%); group III was given 0.02% AAF alone; groups IV and V received both AAF and NaNO2 (0.2 and 0.3% respectively) in their diet for 12 weeks. At the end of the experiment, all rats in groups III, IV and V developed early stage phenomena of hepatocellular carcinoma, including hepatomegaly with variable-sized foci and neoplastic nodules. Severe damage was observed in the rats treated with AAF and NaNO2. Feeding of AAF (0.02%) for 3 months elevated the levels of c-Fos, c-Jun and c-Myc proteins in the rat livers. The AAF-induced c-Jun, c-Fos and c-Myc expressions were significantly magnified (P < 0.001) by NaNO2. These data confirmed that the strengthening of AAF-induced hepatocarcinogenesis by NaNO2 should be associated with its enhancing effect on the AAF-induced increases in the expressions of c-Jun, c-Fos and c-Myc.

摘要

如前所述,2-乙酰氨基芴(AAF)在酸性条件下与亚硝酸烟雾反应生成N-亚硝基-AAF(N-NO-AAF),其毒性和诱变作用比其母体化合物更强。在本研究中,观察了亚硝酸钠(NaNO₂)对喂食AAF和NaNO₂的大鼠中AAF致瘤性的影响。将Wistar大鼠分为五组:第一组作为对照组;第二组用NaNO₂(0.3%)处理;第三组单独给予0.02%的AAF;第四组和第五组在其饮食中同时接受AAF和NaNO₂(分别为0.2%和0.3%),持续12周。实验结束时,第三组、第四组和第五组的所有大鼠均出现了肝细胞癌的早期现象,包括肝脏肿大伴有大小不一的病灶和肿瘤结节。在接受AAF和NaNO₂处理的大鼠中观察到了严重损伤。喂食AAF(0.02%)3个月可提高大鼠肝脏中c-Fos、c-Jun和c-Myc蛋白的水平。NaNO₂显著放大了AAF诱导的c-Jun、c-Fos和c-Myc表达(P < 0.001)。这些数据证实,NaNO₂增强AAF诱导的肝癌发生应与其增强AAF诱导的c-Jun、c-Fos和c-Myc表达增加的作用有关。

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