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The role of chronic irritation and inflammation in tumor promotion in CD-1 mice by petroleum middle distillates.

机译:慢性刺激和炎症在石油中间馏分对CD-1小鼠肿瘤促进中的作用。

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摘要

n initiation-promotion bioassay in CD-1 mice was used to examine the role of chronic irritation and inflammation in tumor promotion by petroleum middle distillates. A representative hydrodesulfurized middle distillate (API 81-07) was selected as the test article. Test groups (54 mice per group) were initiated once with 50 ug of 7,12-dimethylbenzanthracene (DMBA). Promotion with API 81-07 consisted of twice weekly treatments for 25 weeks with either 25 ul, 50 ul, 50 ul + daily treatment with 15 ug dexamethasone, 50 ul + post-application washings, and 100 ul. Three mice from each group were sacrificed at 21 day intervals (24 total per group). The skin from interim sacrificed (IS) mice was examined histopathologically for tumor, acanthosis, hyperkeratosis, pseudo-epitheliomatous hyperplasia, epidermal crusting, and subacute inflammation. In-life observations included examination of all mice for erythema and edema for 8 weeks following the first promotion treatment. Tumor incident at study termination was as follows: 25 ul (45%), 50 ul (43%), 50 ul + dexamethasone (0%), 50 ul + washing (70%), and 100 ul (81%). An overall correlation of
机译:在CD-1小鼠中采用n启动促进生物测定法检查石油中馏分物对慢性刺激和炎症在肿瘤促进中的作用。选择代表性的加氢脱硫中间馏分(API 81-07)作为测试物品。用50μg的7,12-二甲基苯并蒽(DMBA)启动测试组(每组54只小鼠)。使用API​​ 81-07进行的推广包括每周两次两次,持续25周,分别为25 ul,50 ul,50 ul +每日治疗15 ug地塞米松,50 ul +施用后洗液和100 ul。每21天间隔处死每组三只小鼠(每组总共24只)。组织病理学检查了来自中期处死(IS)小鼠的皮肤的肿瘤,棘皮病,角化过度,假性上皮瘤性增生,表皮结cru和亚急性炎症。生命中的观察包括在首次促进治疗后8周内检查所有小鼠的红斑和水肿。研究终止时的肿瘤事件如下:25 ul(45%),50 ul(43%),50 ul +地塞米松(0%),50 ul +洗涤液(70%)和100 ul(81%)。的整体相关性

著录项

  • 作者单位

    The University of Texas School of Public Health.;

  • 授予单位 The University of Texas School of Public Health.;
  • 学科 Health Sciences Public Health.
  • 学位 Ph.D.
  • 年度 1989
  • 页码 299 p.
  • 总页数 299
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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