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红甜菜甜菜红素色素无法引发或促进肝癌发生。

Inability of red beet betalain pigments to initiate or promote hepatocarcinogenesis.

作者信息

Schwartz S J, von Elbe J H, Pariza M W, Goldsworthy T, Pitot H C

出版信息

Food Chem Toxicol. 1983 Oct;21(5):531-5. doi: 10.1016/0278-6915(83)90136-9.

Abstract

A short-term bioassay was used to determine the ability of red-beet betalain pigments to initiate or promote hepatocarcinogenesis in rat liver. Female Sprague-Dawley rats were partially hepatectomized and separated into nine groups (6-11 animals/group). Four of the groups were treated with betacyanin pigment preparations (betacyanin solution after fermentation, 50 mg/kg; pure betanin, 50 mg/kg; degraded betanin, 50 mg/kg; a betacyanin diet containing 2000 ppm/kg) to evaluate their ability to initiate hepatocarcinogenesis. N-Nitrosodiethylamine (NDEA: 10 mg/kg) was used for the positive control. Another group, previously initiated with NDEA, received daily a betacyanin solution (100 ppm; 3.5 mg/rat/day) to determine the pigment's ability to promote NDEA hepatocarcinogenesis in comparison with positive and negative controls treated respectively with and without a promoting agent (0.5% phenobarbital in the diet). Animals were killed after month 6 (promotion test) or 8 (initiation test). Liver sections were stained with haematoxylin and eosin and for gamma-glutamyl transpeptidase (GGT) activity. The number of enzyme-altered foci and the percentage of liver volume so affected, were determined for each group, by scoring for GGT. Comparison of the results obtained for the experimental groups with those for positive and negative control groups indicated that the betacyanin pigments tested in this assay did not initiate or promote hepatocarcinogenesis in rat liver. These findings provide further evidence that betalain colourants may be viable alternatives for synthetic dyes currently used as food additives.

摘要

采用短期生物测定法来确定红甜菜甜菜红素色素引发或促进大鼠肝脏肝癌发生的能力。对雌性斯普拉格-道利大鼠进行部分肝切除,并分为九组(每组6 - 11只动物)。其中四组用花青素色素制剂处理(发酵后的花青素溶液,50毫克/千克;纯甜菜苷,50毫克/千克;降解甜菜苷,50毫克/千克;含2000 ppm/千克的花青素饮食),以评估它们引发肝癌发生的能力。N-亚硝基二乙胺(NDEA:10毫克/千克)用作阳性对照。另一组先前用NDEA启动,每天接受花青素溶液(100 ppm;3.5毫克/大鼠/天),以确定该色素与分别用促进剂(饮食中含0.5%苯巴比妥)和不用促进剂处理的阳性和阴性对照相比促进NDEA诱导肝癌发生的能力。在第6个月(促进试验)或第8个月(启动试验)后处死动物。肝切片用苏木精和伊红染色,并检测γ-谷氨酰转肽酶(GGT)活性。通过对GGT评分,确定每组酶改变灶的数量以及受影响的肝脏体积百分比。将实验组获得的结果与阳性和阴性对照组的结果进行比较,表明该测定中测试的花青素色素不会引发或促进大鼠肝脏的肝癌发生。这些发现进一步证明甜菜红素着色剂可能是目前用作食品添加剂的合成染料的可行替代品。

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