Suppr超能文献

衰老小鼠中二乙基亚硝胺致癌作用的时间进程

Temporal advancement of diethylnitrosamine carcinogenesis in aging mice.

作者信息

Clapp N K, Perkins E H, Klima W C, Cacheiro L H

出版信息

J Gerontol. 1981 Mar;36(2):158-63. doi: 10.1093/geronj/36.2.158.

Abstract

Female BALB/c mice were given diethylnitrosamine (DEN) in their drinking water beginning at 2.5, 9.5, and 17 months of age (cumulative dose approximately 300 to 400 mg/kg body weight) or were untreated. Median times of death for the treatment groups were 193, 168, and 125 days, respectively, after cessation of DEN treatment and were significantly different (p less than .01). Induced tumors in the three respective age groups were of squamous forestomach (88, 87, and 84%), vascular tumors of the liver (11, 13, and 16%), and adenomas of the lung (65, 56, and 54%). Controls had no forestomach or liver tumors and relatively low incidences of lung tumors. The fact that aging mice have similar incidences and types of tumors of the same size and in the same tissues, but at an earlier time, shows that (1) DEN is carcinogenic in aging BALB/c mice; (2) age at treatment does not alter the tumor-susceptible tissue nor types of tumors after DEN treatment; (3) tumor incidences are not affected by age at time of treatment; (4) mice die earlier with induced tumors with increasing age at time of treatment; (5) age-matched non-DEN-treated mice die from different diseases (leukemias) than do DEN-treated mice (stomach and liver tumors). These observations may be related, in part, to an identified age-dependent decrease in immunocompetency or to other age-related changes, such as vascular or hormonal, which could explain temporal advancement in the tumorigenic process.

摘要

雌性BALB/c小鼠在2.5、9.5和17月龄时开始饮用含二乙基亚硝胺(DEN)的水(累积剂量约为300至400mg/kg体重),或不进行处理。各处理组在停止DEN处理后的中位死亡时间分别为193、168和125天,且差异显著(p小于0.01)。三个相应年龄组诱导产生的肿瘤分别为鳞状前胃肿瘤(88%、87%和84%)、肝血管肿瘤(11%、13%和16%)和肺腺瘤(65%、56%和54%)。对照组无前胃或肝肿瘤,肺肿瘤发生率相对较低。衰老小鼠在相同大小的相同组织中具有相似的肿瘤发生率和类型,但时间更早,这一事实表明:(1)DEN对衰老的BALB/c小鼠具有致癌性;(2)处理时的年龄不会改变DEN处理后肿瘤易感组织或肿瘤类型;(3)肿瘤发生率不受处理时年龄的影响;(4)随着处理时年龄的增加,诱导肿瘤的小鼠死亡更早;(5)年龄匹配的未接受DEN处理的小鼠死于与接受DEN处理的小鼠不同的疾病(白血病)(胃和肝肿瘤)。这些观察结果可能部分与已确定的年龄依赖性免疫能力下降或其他与年龄相关的变化有关,如血管或激素变化,这可以解释肿瘤发生过程中的时间提前。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验