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首页> 外文期刊>Food and Chemical Toxicology: An International Journal Published for the British Industrial Biological Research >Lack of chemopreventive effects of alpha-eleostearic acid on 7,12-dimethylbenz(a)anthracene (DMBA) and 1,2-dimethylhydrazine (DMH)-induced mammary and colon carcinogenesis in female Sprague-Dawley rats.
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Lack of chemopreventive effects of alpha-eleostearic acid on 7,12-dimethylbenz(a)anthracene (DMBA) and 1,2-dimethylhydrazine (DMH)-induced mammary and colon carcinogenesis in female Sprague-Dawley rats.

机译:缺乏对雌性Sprague-Dawley大鼠的7,12-二甲基苯并(a)蒽(DMBA)和1,2-二甲基肼(DMH)诱导的乳腺和结肠癌发生的化学预防作用。

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摘要

alpha-Eleostearic acid is one of the conjugated linolenic acids from tung oil, which is obtained from the seeds of Aleurites fordii. The effects of dietary alpha-eleostearic acid (18:3, n-5) on the post-initiation period of 7,12-dimethylbenz[a]anthracene (DMBA) and 1,2-dimethylhydrazine (DMH)-induced mammary and colon carcinogenesis were examined using female Sprague-Dawley (SD) rats. For initiation, rats were given subcutaneous injections of 40mg/kg body weight (5 times) and 20mg/kg body weight (3 times) of DMH during the age of 6-8 weeks and a single intragastric administration of 50mg/kg body weight of DMBA at 9 weeks. Then, the animals were treated with 0%, 0.01%, 0.1% or 1.0% alpha-eleostearic acid for 34 weeks. Control rats received the basal diet alone or 1.0% alpha-eleostearic acid without prior initiation treatment. All surviving animals were killed at week 37 of the experiment. There were no statistically significant alterations in any of the parameters for either mammary or colon tumors. These results thus indicate that alpha-eleostearic acid does not exert clear modification effects on DMBA and DMH-induced mammary and colon carcinogenesis, at least under the present experimental conditions.
机译:α-油硬脂酸是来自桐油的共轭亚麻酸之一,其是从Foreur的Aleurites种子中获得的。日粮α-硬脂酸(18:3,n-5)对7,12-二甲基苯并[a]蒽(DMBA)和1,2-二甲基肼(DMH)诱导的乳腺和结肠的启动后期的影响使用雌性Sprague-Dawley(SD)大鼠检查其致癌作用。首先,在6-8周内给大鼠皮下注射40毫克/千克体重(5倍)和20毫克/千克体重(3倍)的DMH,单次胃内注射50毫克/千克体重的DMH。 9周的DMBA。然后,用0%,0.01%,0.1%或1.0%的α-硬脂酸治疗动物34周。对照组大鼠仅接受基础饮食或1.0%α-硬脂酸,无需事先开始治疗。在实验的第37周将所有存活的动物杀死。乳腺或结肠肿瘤的任何参数均无统计学上的显着变化。因此,这些结果表明,至少在目前的实验条件下,α-硬脂酸对DMBA和DMH诱导的乳腺和结肠癌发生没有明显的修饰作用。

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