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环境污染物邻苯二甲酸二(2-乙基己基)酯对苯巴比妥的抑制作用以及膳食胆碱缺乏会促进大鼠肝脏的癌前病变。

Inhibition of phenobarbital and dietary choline deficiency promoted preneoplastic lesions in rat liver by environmental contaminant di(2-ethylhexyl)phthalate.

作者信息

DeAngelo A B, Garrett C T, Queral A E

出版信息

Cancer Lett. 1984 Jul;23(3):323-30. doi: 10.1016/0304-3835(84)90100-9.

Abstract

The effect of di(2-ethylhexyl)phthalate (DEHP), a widely used plasticizer and environmental contaminant, on the emergence of gamma-glutamyltranspeptidase positive (GGT+) preneoplastic foci in the liver of rats fed promoting diets was studied. GGT+ foci were initiated in the liver of Sprague--Dawley male rats with a single dose of diethylnitrosamine (DEN) following partial hepatectomy. One series of control rats received saline vehicle alone. Promotion of foci was commenced by feeding: (1) a choline-deficient diet (CD); (2) a choline-supplemented diet (CS) containing 0.06% phenobarbital (CS + PHB); or (3) a CD diet containing 0.06% phenobarbital (CD + PHB). In the absence of initiation by DEN, dietary treatments did not increase the number of GGT+ foci. In rats receiving DEN, each promoting regimen effectively increased the number of GGT+ foci above levels in control rats fed only the choline-supplemented diet. Inclusion of the plasticizer at a level of 2% in each of the dietary promotion treatments, however, effectively inhibited the appearance of the foci.

摘要

研究了广泛使用的增塑剂和环境污染物邻苯二甲酸二(2-乙基己基)酯(DEHP)对喂食促癌饮食的大鼠肝脏中γ-谷氨酰转肽酶阳性(GGT+)癌前病灶出现的影响。在部分肝切除术后,用单剂量二乙基亚硝胺(DEN)在斯普拉格-道利雄性大鼠肝脏中引发GGT+病灶。一组对照大鼠仅接受生理盐水载体。通过喂食开始促进病灶发展:(1)胆碱缺乏饮食(CD);(2)含有0.06%苯巴比妥的胆碱补充饮食(CS+PHB);或(3)含有0.06%苯巴比妥的CD饮食(CD+PHB)。在没有DEN引发的情况下,饮食处理不会增加GGT+病灶的数量。在接受DEN的大鼠中,每种促癌方案都有效地使GGT+病灶的数量增加到仅喂食胆碱补充饮食的对照大鼠的水平之上。然而,在每种饮食促癌处理中加入2%水平的增塑剂,有效地抑制了病灶的出现。

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