咖啡酸刺激F344雄性大鼠前胃和肾脏细胞分裂的剂量效应

Ursula Lutz , Serena Lugli , Annette Bitsch , Josef Schlatter , Werner K. Lutz
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引用次数: 15

摘要

饮食中2%的咖啡酸(CA, 3,4-二羟基肉桂酸)已被证明对F344大鼠和B6C3F1小鼠的前胃和肾脏具有致癌作用。根据它在咖啡和许多食物中的含量,以及对剂量0到2%之间的癌症发病率进行线性插值,人类的癌症风险将是相当大的。在两种靶器官中,肿瘤形成之前都有增生,这可能是致癌作用的主要机制。在饲喂饲粮不同浓度CA(0、0.05、0.14、0.40和1.64%)4周后,对雄性F344大鼠进行了剂量-反应关系研究。腹腔注射5-溴-2′-脱氧尿苷(BrdU) 2小时后,通过免疫组化分析观察DNA复制s期的细胞。前胃每毫米切片长度上皮细胞总数和brdu阳性细胞单位长度标记指数(ULLI)均增加约2.5倍,分别为0.40和1.64%。最低浓度(0.05%)无影响。在0.14%时,两个变量都减少了约三分之一。在肾脏中,近端小管细胞的标记指数也呈j型(或u型)剂量反应,增加1.8倍,达到1.64%。在非靶器官的腺胃和肝中,未见剂量相关效应。数据显示,器官特异性的癌症诱导和细胞分裂的刺激之间有良好的相关性。关于剂量-反应关系和动物肿瘤数据对人类癌症风险的相应外推,线性外推似乎不合适。
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Dose Response for the Stimulation of Cell Division by Caffeic Acid in Forestomach and Kidney of the Male F344 Rat

Caffeic acid (CA, 3,4-dihydroxycinnamic acid), at 2% in the diet, had been shown to be carcinogenic in forestomach and kidney of F344 rats and B6C3F1 mice. Based on its occurrence in coffee and numerous foods and using a linear interpolation for cancer incidence between dose 0 and 2%, the cancer risk in humans would be considerable. In both target organs, tumor formation was preceded by hyperplasia, which could represent the main mechanism of carcinogenic action. The dose–response relationship for this effect was investigated in male F344 rats after 4-week feeding with CA at different dietary concentrations (0, 0.05, 0.14, 0.40, and 1.64%). Cells in S-phase of DNA replication were visualized by immunohistochemical analysis of incorporated 5-bromo-2′-deoxyuridine (BrdU), 2 hr after intraperitoneal injection. In the forestomach, both the total number of epithelial cells per millimeter section length and the unit length labeling index of BrdU-positive cells (ULLI) were increased, about 2.5-fold, at 0.40 and 1.64%. The lowest concentration (0.05%) had no effect. At 0.14%, both variables were decreased by about one-third. In the kidney, the labeling index in proximal tubular cells also indicated a J-shaped (or U-shaped) dose response with a 1.8-fold increase at 1.64%. In the glandular stomach and in the liver, which are not target organs, no dose-related effect was seen. The data show a good correlation between the organ specificity for cancer induction and stimulation of cell division. With respect to the dose–response relationship and the corresponding extrapolation of the animal tumor data to a human cancer risk, a linear extrapolation appears not to be appropriate.

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