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饮食对大鼠肝癌发生起始和促进阶段的影响。

Dietary effects on initiation and promotion of hepatocarcinogenesis in rat.

作者信息

Hendrich S, Glauert H P, Pitot H C

机构信息

McArdle Laboratory for Cancer Research, University of Wisconsin, Madison.

出版信息

J Cancer Res Clin Oncol. 1988;114(2):149-57. doi: 10.1007/BF00417829.

Abstract

Female F344/N rats were initiated with DEN (10 mg/kg) 24 h after a 70% partial hepatectomy. Groups of 10 rats were fed (a) AIN, group-1; (b) PD, group-2; or (c) NIH, group-3, for 1 week after initiation and were then fed NIH plus the promoting agent PB at a level of 0.05% in the diets for 6 months. Other groups were fed NIH for 1 week after initiation and then NIH without PB (group-4), AIN + PB (group-5), AIN without PB (group-6), PD + PB (group-7), or PD without PB (group-8) for 6 months. The numbers and volume percentages of AHF were quantified by stereologic methods from frozen serial sections, stained consecutively for GGT, ATPase, and G6Pase. For the groups fed different diets during the 1st week after initiation, the numbers and volume of AHF were significantly greater in group-2 than in groups 1 or 3. The numbers of AHF were significantly less in group-3 than in group-1. The numbers and volume of AHF were significantly greater in groups fed PB during the promotion phase, except in the case of group-7, whose focal volume did not differ from groups 6 or 8. Group-3 had significantly greater numbers of AHF than groups 5 and 7. These findings can be explained by the hypothesis that the NIH diet contained factors that acted synergistically with PB to enhance tumor promotion. The mean focal volume of both GGT positive and ATPase negative foci was significantly greater in group-5 than in all other groups; this indicates that the AIN + PB regimen selectively promoted the growth of a subpopulation of AHF. These findings show that alterations in the composition of diets fed during hepatocarcinogenesis significantly alter the effects of specific chemical agents acting during the stages of initiation and promotion in hepatocarcinogenesis.

摘要

雌性F344/N大鼠在70%部分肝切除术后24小时用二乙基亚硝胺(DEN,10毫克/千克)启动。启动后,将10只大鼠分为一组喂食AIN(第1组)、一组喂食PD(第2组)、一组喂食NIH(第3组),持续1周,然后在接下来的6个月里,喂食添加了0.05%促癌剂PB的NIH饲料。其他组在启动后喂食NIH 1周,然后在接下来的6个月里分别喂食不添加PB的NIH(第4组)、添加PB的AIN(第5组)、不添加PB的AIN(第6组)、添加PB的PD(第7组)或不添加PB的PD(第8组)。通过体视学方法,从连续冰冻切片中对谷氨酰转肽酶(GGT)、三磷酸腺苷酶(ATPase)和葡萄糖-6-磷酸酶(G6Pase)进行连续染色,对非典型增生灶(AHF)的数量和体积百分比进行定量分析。在启动后第1周喂食不同饲料的组中,第2组的AHF数量和体积显著大于第1组或第3组。第3组的AHF数量显著少于第1组。在促癌阶段喂食PB的组中,AHF的数量和体积显著增加,但第7组除外,其病灶体积与第6组或第8组无差异。第3组的AHF数量显著多于第5组和第7组。这些发现可以通过以下假设来解释:NIH饲料中含有与PB协同作用以增强肿瘤促进作用的因子。第5组中GGT阳性且ATPase阴性病灶的平均灶体积显著大于所有其他组;这表明AIN + PB方案选择性地促进了AHF亚群的生长。这些发现表明,肝癌发生过程中所喂食饲料成分的改变,显著改变了在肝癌发生的启动和促癌阶段起作用的特定化学物质的效果。

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