Hoover K L, Lynch P H, Poirier L A
J Natl Cancer Inst. 1984 Dec;73(6):1327-36.
The potential promoting and/or complete carcinogenic activity of a methyl group-deficient (MD) diet lacking methionine, choline, vitamin B12, and folate on liver tumor induction in weanling male F344/NCr rats was examined. Each of 50 rats per group received one injection 20 mg diethylnitrosamine [(DENA) CAS: 55-18-5; N-nitrosodiethylamine]/kg body weight at 4 weeks of age, and then each was maintained on a methyl group-adequate (MA) diet for 52 weeks (groups 2 and 5) or on an MD diet for 15 weeks followed by the MA diet for 37 weeks (group 4). Controls received injections of saline and were maintained on the same two respective diet regimens (groups 1 and 3, respectively). Histologic results from sacrifices at 6, 10, 15, 22, 39, and 52 weeks revealed early development of foci of eosinophilic gamma-glutamyltransferase (GGT)-positive hepatocytes by week 6 in DENA-MD diet-treated rats, with subsequent development of a diffuse hyperplasia of hepatocytes, oval cell proliferation, cholangiofibrosis, nodular cirrhosis, and neoplastic nodule (NN) formation and, at 52 weeks, hepatocellular carcinomas (HCC) in 13 of 15 rats. Similar but significantly fewer lesions were observed at slightly later sacrifice times in the livers of saline-MD diet-treated rats, with development of NN in 5 of 12 rats and an HCC in 1 of 12 rats at 52 weeks. DENA-treated rats on MA diets developed relatively few GGT-positive foci, and none developed any neoplastic lesions. Except for basophilic foci, areas and foci of cellular alteration containing glycogen-rich hepatocytes frequently exhibited diminished uptake of injected iron and decreased glucose-6-phosphatase and ATPase contents focally or throughout. This study indicates that a relatively brief exposure of both untreated and DENA-treated weanling rats to a severely MD diet produces classical preneoplastic and neoplastic lesions in their livers.
研究了缺乏蛋氨酸、胆碱、维生素B12和叶酸的甲基缺乏(MD)饮食对断奶雄性F344/NCr大鼠肝脏肿瘤诱导的潜在促进和/或完全致癌活性。每组50只大鼠在4周龄时每只接受一次20毫克二乙基亚硝胺[(DENA)CAS:55-18-5;N-亚硝基二乙胺]/千克体重的注射,然后每只大鼠维持甲基充足(MA)饮食52周(第2组和第5组)或MD饮食15周,随后MA饮食37周(第4组)。对照组接受生理盐水注射,并分别维持相同的两种饮食方案(分别为第1组和第3组)。在第6、10、15、22、39和52周处死时的组织学结果显示,在DENA-MD饮食处理的大鼠中,到第6周时嗜酸性γ-谷氨酰转移酶(GGT)阳性肝细胞灶早期出现,随后出现肝细胞弥漫性增生、卵圆细胞增殖、胆管纤维化、结节性肝硬化和肿瘤结节(NN)形成,在第52周时,15只大鼠中有13只发生肝细胞癌(HCC)。在生理盐水-MD饮食处理的大鼠肝脏中,在稍晚的处死时间观察到类似但明显较少的病变,在第52周时,12只大鼠中有5只发生NN,12只大鼠中有1只发生HCC。接受MA饮食的DENA处理大鼠产生相对较少的GGT阳性灶,且无一发生任何肿瘤性病变。除嗜碱性灶外,含有富含糖原肝细胞的细胞改变区域和灶通常局部或整体表现为注射铁摄取减少、葡萄糖-6-磷酸酶和ATP酶含量降低。本研究表明,未处理和DENA处理的断奶大鼠相对短暂地暴露于严重的MD饮食中,会在其肝脏中产生典型的癌前和肿瘤性病变。