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喂食甲基缺乏、氨基酸限定饮食的大鼠的肝癌发生

Hepatocarcinogenesis in rats fed methyl-deficient, amino acid-defined diets.

作者信息

Mikol Y B, Hoover K L, Creasia D, Poirier L A

出版信息

Carcinogenesis. 1983 Dec;4(12):1619-29. doi: 10.1093/carcin/4.12.1619.

DOI:10.1093/carcin/4.12.1619
PMID:6317218
Abstract

The ability of methyl-deficient, amino acid-defined diets to produce liver tumors was studied in rats treated both with and without initiating doses of diethylnitrosamine (DENA). Male, weanling F344 rats were fed a complete, amino acid-defined diet for one week. They were then injected once i.p. with one of 3 doses of DENA (20, 70 or 200 mg/kg body weight) and fed the complete diet for an additional week. Thirty animals from each dose group were then maintained for 76 weeks on the complete diet (Diet 1) or one of 4 methyl-deficient diets: Diet 2, devoid of methionine and choline; Diet 3, devoid of methionine only; Diet 4, devoid of choline only and Diet 5, devoid of methionine, choline, folic acid and vitamin B12. In Diets 2, 3 and 5 methionine was replaced by equimolar amounts of its metabolic precursor DL-homocystine. Control rats were injected i.p. with the saline vehicle and maintained for the 76-week period on Diets 1 and 2. Forty percent of the rats fed Diet 2, but receiving no DENA, developed hepatocellular carcinomas or cholangiomas. A 90-100% incidence of hepatocellular carcinomas was seen in all groups initiated with DENA and fed Diet 2. No malignant liver tumors developed in Diet 1 rats that had received 0 or 20 mg/kg DENA; however, hepatocellular carcinomas were noted in one-half of such animals receiving the 70 and 200 mg/kg doses. Liver metastases grew in the lungs of 60% of the tumor-bearing rats fed Diet 2; none were seen in the Diet 1-fed rats. The singly deficient Diets 3 and 4 enhanced liver tumor formation to DENA-initiated rats to a significantly lesser extent than did Diet 2. All DENA-initiated rats fed the severely deficient Diet 5, died within 23 experimental weeks with livers containing hepatocytes of atypical appearance and, particularly at the 2 higher dosages, a cirrhotic pseudonodular architecture. No hepatocellular carcinomas or cholangiomas were observed in Diet 5-fed rats. None of the diets tested appeared to enhance tumor formation in extrahepatic tissues. In fact, significant decreases were noted in the formation of spontaneous testicular interstitial cell tumors in Diet 2-fed rats and of pancreatic acinar tumors in rats fed Diets 2 and 3. Diet 2, devoid of both methionine and choline, also induced metaplasia of pancreatic acinar cells to hepatocyte-like cells and was associated with moderate to severe hyperplasia of the transitional epithelium lining the renal pelvis.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

在给予和未给予起始剂量二乙基亚硝胺(DENA)的大鼠中,研究了甲基缺乏、氨基酸限定饮食诱发肝肿瘤的能力。雄性断乳F344大鼠先喂饲完整的氨基酸限定饮食一周。然后经腹腔注射3种剂量之一的DENA(20、70或200mg/kg体重),并再喂饲完整饮食一周。然后,每个剂量组的30只动物分别用完整饮食(饮食1)或4种甲基缺乏饮食之一维持76周:饮食2,缺乏蛋氨酸和胆碱;饮食3,仅缺乏蛋氨酸;饮食4,仅缺乏胆碱;饮食5,缺乏蛋氨酸、胆碱、叶酸和维生素B12。在饮食2、3和5中,蛋氨酸被等摩尔量的其代谢前体DL-高半胱氨酸替代。对照大鼠经腹腔注射生理盐水载体,并在饮食1和2上维持76周。喂饲饮食2但未接受DENA的大鼠中,40%发生肝细胞癌或胆管瘤。在所有用DENA启动并喂饲饮食2的组中,肝细胞癌的发生率为90%-100%。接受0或20mg/kg DENA的饮食1大鼠未发生恶性肝肿瘤;然而,接受70和200mg/kg剂量的此类动物中有一半出现肝细胞癌。在喂饲饮食2的荷瘤大鼠中,60%的大鼠肺部出现肝转移;在喂饲饮食1的大鼠中未观察到肝转移。单一缺乏的饮食3和4对DENA启动的大鼠肝肿瘤形成的促进作用明显小于饮食2。所有喂饲严重缺乏的饮食5的DENA启动大鼠在23个实验周内死亡,其肝脏含有外观异常的肝细胞,特别是在2个较高剂量时,出现肝硬化假结节结构。在喂饲饮食5的大鼠中未观察到肝细胞癌或胆管瘤。所测试的任何饮食似乎均未促进肝外组织中的肿瘤形成。事实上,在喂饲饮食2的大鼠中,自发性睾丸间质细胞瘤的形成以及在喂饲饮食2和3的大鼠中胰腺腺泡肿瘤的形成均显著减少。缺乏蛋氨酸和胆碱的饮食2还诱导胰腺腺泡细胞化生为肝细胞样细胞,并伴有肾盂内衬的移行上皮中度至重度增生。(摘要截短至400字)

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