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低剂量联合使用10种杂环胺处理大鼠对肝脏病灶发展的协同增强作用。

Synergistic enhancement of hepatic foci development by combined treatment of rats with 10 heterocyclic amines at low doses.

作者信息

Hasegawa R, Miyata E, Futakuchi M, Hagiwara A, Nagao M, Sugimura T, Ito N

机构信息

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

出版信息

Carcinogenesis. 1994 May;15(5):1037-41. doi: 10.1093/carcin/15.5.1037.

Abstract

Potential synergism between 10 carcinogenic heterocyclic amines [3-amino-1,4-dimethyl-5H-pyrido[4,3-b]indole (Trp-P-1), 3-amino-1-methyl-5H-pyrido[4,3-b]indole (Trp-P-2), 2-amino-6 methyldipyrido[1,2-a:3',2'-d]imidazole (Glu-P-1), 2-amino-dipyrido[1,2-a:3',2'-d]imidazole (Glu-P-2), 2-amino-3-methylimidazo[4,5-f]quinoline (IQ), 2-amino-3,4-dimethyl-imidazo[4,5-f]quinoline (MeIQ), 2-amino-3,8-dimethyl-imidazo[4,5-f]quinoxaline (MeIQx), 2-amino-3-methyl-9H-pyrido[2,3-b]indole (MeA alpha C), 2-amino-9H-pyrido[2,3-b]indole (A alpha C) and 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP)] in rat liver carcinogenesis was examined. Male F344 rats were initially given diethylnitrosamine (200 mg/kg, i.p.) and beginning 2 weeks later received heterocyclic amines individually at doses 1/10 of that proven to be carcinogenic or in combination at 1/10 or 1/100 doses for 6 weeks. All animals were subjected to partial hepatectomy at week 3 and killed at week 8. The induction of immunohistochemically demonstrable placental glutathione S-transferase positive foci was significantly increased in rats given all 10 chemicals in combination at the 1/10 dose level while values were almost the same as in controls with the 1/100 dose mixture and the individual chemicals, except for Glu-P-1 which significantly increased foci development and Glu-P-2 and A alpha c which significantly decreased levels of foci at the 1/10 dose level. Thus apparent synergism was observed with the 1/10 dose level combination. When the data are considered together with our previous results obtained with five heterocyclic amines using 1/1, 1/5 and 1/25 dose levels, combined effects were found to be related to the number of chemicals included and the dose levels of each, with a possible isoadditive influence being common. The findings are of particular significance since heterocyclic amines and other carcinogenic agents might be simultaneously generated during cooking.

摘要

研究了10种致癌杂环胺[3-氨基-1,4-二甲基-5H-吡啶并[4,3-b]吲哚(Trp-P-1)、3-氨基-1-甲基-5H-吡啶并[4,3-b]吲哚(Trp-P-2)、2-氨基-6-甲基二吡啶并[1,2-a:3',2'-d]咪唑(Glu-P-1)、2-氨基二吡啶并[1,2-a:3',2'-d]咪唑(Glu-P-2)、2-氨基-3-甲基咪唑并[4,5-f]喹啉(IQ)、2-氨基-3,4-二甲基咪唑并[4,5-f]喹啉(MeIQ)、2-氨基-3,8-二甲基咪唑并[4,5-f]喹喔啉(MeIQx)、2-氨基-3-甲基-9H-吡啶并[2,3-b]吲哚(MeAαC)、2-氨基-9H-吡啶并[2,3-b]吲哚(AαC)和2-氨基-1-甲基-6-苯基咪唑并[4,5-b]吡啶(PhIP)]在大鼠肝癌发生过程中的潜在协同作用。雄性F344大鼠最初腹腔注射二乙基亚硝胺(200mg/kg),2周后开始分别给予剂量为已证实致癌剂量1/10的杂环胺,或按1/10或1/100剂量联合给予,持续6周。所有动物在第3周接受部分肝切除术,并在第8周处死。在1/10剂量水平联合给予所有10种化学物质的大鼠中,免疫组化可检测到的胎盘谷胱甘肽S-转移酶阳性灶的诱导显著增加,而在1/100剂量混合物和单独使用化学物质的情况下,其值与对照组几乎相同,但Glu-P-1在1/10剂量水平时显著增加灶的形成,Glu-P-2和AαC在1/10剂量水平时显著降低灶的水平。因此,在1/10剂量水平联合使用时观察到明显的协同作用。当将这些数据与我们之前使用1/1、1/5和1/25剂量水平的五种杂环胺获得的结果综合考虑时,发现联合效应与所含化学物质的数量及其各自的剂量水平有关,可能存在共同的等加性影响。这些发现具有特别重要的意义,因为杂环胺和其他致癌剂可能在烹饪过程中同时产生。

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