Mauderly Joe L, Gigliotti Andrew P, Barr Edward B, Bechtold William E, Belinsky Steven A, Hahn Fletcher F, Hobbs Charles A, March Thomas H, Seilkop Steven K, Finch Gregory L
Lovelace Respiratory Research Institute, Albuquerque, New Mexico 87108, USA.
Toxicol Sci. 2004 Oct;81(2):280-92. doi: 10.1093/toxsci/kfh203. Epub 2004 Jun 22.
An animal model of lung carcinogenicity induced by chronic inhalation of mainstream cigarette smoke would be useful for research on carcinogenic mechanisms, smoke composition-response relationships, co-carcinogenicity, and chemoprevention. A study was conducted to determine if chronic whole-body exposures of rats would significantly increase lung tumor incidence. Male and female F344 rats (n = 81 to 178/gender) were exposed whole-body 6 h/day, 5 days/week for up to 30 months to smoke from 1R3 research cigarettes diluted to 100 (LS) or 250 (HS) mg total particulate matter/m(3), or sham-exposed to clean air (C). Gross respiratory tract lesions and standard lung and nasal sections were evaluated by light microscopy. A slight reduction of survival suggested that the HS level was at the maximum tolerated dose as commonly defined. Cigarette smoke exposure significantly increased the incidences of non-neoplastic and neoplastic proliferative lung lesions in females, while nonsignificant increases were observed in males. The combined incidence of bronchioloalveolar adenomas and carcinomas in females were: HS = 14%; LS = 6%; and C = 0%. These incidences represented minima because only standard lung sections and gross lesions were evaluated. Mutations in codon 12 of the K-ras gene occurred in 4 of 23 (17%) tumors. Three mutations were G to A transitions and one was a G to T transversion. The incidence of neoplasia of the nasal cavity was significantly increased at the HS, but not the LS level in both males and females (HS = 6%, LS = 0.3%, C = 0.4% for combined genders). These results demonstrate that chronic whole-body exposure of rats to cigarette smoke can induce lung cancer.
慢性吸入主流香烟烟雾诱导的肺癌动物模型,对于致癌机制、烟雾成分 - 反应关系、协同致癌作用和化学预防的研究将是有用的。进行了一项研究以确定大鼠的慢性全身暴露是否会显著增加肺癌发生率。将雄性和雌性F344大鼠(每组81至178只)每天全身暴露6小时,每周5天,长达30个月,使其吸入稀释至总颗粒物100(低剂量组,LS)或250(高剂量组,HS)mg/m³的1R3研究香烟烟雾,或假暴露于清洁空气(对照组,C)。通过光学显微镜评估大体呼吸道病变以及标准的肺和鼻组织切片。生存率略有降低表明高剂量组处于通常定义的最大耐受剂量。香烟烟雾暴露显著增加了雌性非肿瘤性和肿瘤性增殖性肺部病变的发生率,而雄性中观察到的增加不显著。雌性细支气管肺泡腺瘤和癌的合并发生率分别为:高剂量组 = 14%;低剂量组 = 6%;对照组 = 0%。这些发生率为最低值,因为仅评估了标准肺组织切片和大体病变。23个肿瘤中有4个(17%)发生了K-ras基因第12密码子的突变。3个突变是G到A的转换,1个是G到T的颠换。鼻腔肿瘤发生率在高剂量组显著增加,但低剂量组在雄性和雌性中均未增加(两性合并高剂量组 = 6%,低剂量组 = 0.3%,对照组 = 0.4%)。这些结果表明,大鼠慢性全身暴露于香烟烟雾可诱发肺癌。