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用氢氯氟烃123对大鼠进行的两年吸入毒性研究。

Two-year inhalation toxicity study in rats with hydrochlorofluorocarbon 123.

作者信息

Malley L A, Carakostas M, Hansen J F, Rusch G M, Kelly D P, Trochimowicz H J

机构信息

E. I. du Pont de Nemours and Company, Haskell Laboratory for Toxicology and Industrial Medicine, Newark, Delaware 19714, USA.

出版信息

Fundam Appl Toxicol. 1995 Apr;25(1):101-14. doi: 10.1006/faat.1995.1044.

Abstract

The potential chronic toxicity and oncogenicity of hydrochlorofluorocarbon 123 (HCFC-123) was evaluated by exposing male and female rats to 0, 300, 1000, or 5000 ppm HCFC-123 for 6 hr/day, 5 days/week, for 2 years. Clinical pathology was evaluated at 6, 12, 18, and 24 months. An interim termination and measurements of hepatic cell proliferation and beta-oxidation activity were conducted at 12 months. The terminal euthanization occurred at 24 months. Males and females exposed to 5000 ppm and females exposed to 300 or 1000 ppm had lower body weights and body weight gains. Serum triglyceride and glucose concentrations were significantly decreased at all exposure concentrations in both sexes. Serum cholesterol was also lower in 300, 1000, and 5000 ppm females and in 5000 ppm males. Alterations in serum protein concentrations occurred at 300, 1000, and 5000 ppm. Survival was higher in 1000 and 5000 ppm males and females. At 24 months, increased relative liver weight occurred in 5000 ppm males, and decreased absolute kidney weight occurred in 5000 ppm males and in 1000 and 5000 ppm females. Benign hepatocellular adenomas were increased in 5000 ppm males and in all test groups of females. Hepatic cholangiofibromas were also increased in 5000 ppm females. Pancreatic acinar cell adenomas were increased in all test groups of males, and acinar cell hyperplasia was increased in the 1000 and 5000 ppm males and females. Benign testicular interstitial adenomas and focal interstitial cell hyperplasia were also increased in all male test groups compared to controls. Diffuse retinal atrophy was increased in all male and female test groups, but it was considered to be an indirect compound-related effect. Hepatic beta-oxidation activity (peroxisome proliferation) was higher in 300, 1000 and 5000 ppm males and 1000 and 5000 ppm females. Compound-related differences in the rate of hepatic cell proliferation were not observed at any exposure concentration. Decreased incidences of a variety of age-related lesions occurred at 1000 and 5000 ppm.

摘要

通过让雄性和雌性大鼠每天6小时、每周5天暴露于0、300、1000或5000 ppm的氢氯氟烃123(HCFC - 123)中,持续2年,评估了HCFC - 123的潜在慢性毒性和致癌性。在第6、12、18和24个月评估临床病理学。在第12个月进行中期处死并测量肝细胞增殖和β - 氧化活性。在第24个月进行终末安乐死。暴露于5000 ppm的雄性和雌性以及暴露于300或1000 ppm的雌性体重和体重增加较低。在所有暴露浓度下,两性的血清甘油三酯和葡萄糖浓度均显著降低。300、1000和5000 ppm的雌性以及5000 ppm的雄性血清胆固醇也较低。在300、1000和5000 ppm时血清蛋白浓度发生改变。1000和5000 ppm的雄性和雌性存活率较高。在24个月时,5000 ppm的雄性相对肝脏重量增加,5000 ppm的雄性以及1000和5000 ppm的雌性绝对肾脏重量降低。5000 ppm的雄性和所有雌性试验组中良性肝细胞腺瘤增加。5000 ppm的雌性肝胆管纤维瘤也增加。所有雄性试验组中胰腺腺泡细胞腺瘤增加,1000和5000 ppm的雄性和雌性腺泡细胞增生增加。与对照组相比,所有雄性试验组中良性睾丸间质腺瘤和局灶性间质细胞增生也增加。所有雄性和雌性试验组中弥漫性视网膜萎缩增加,但这被认为是与化合物相关的间接效应。300、1000和5000 ppm的雄性以及1000和5000 ppm的雌性肝β - 氧化活性(过氧化物酶体增殖)较高。在任何暴露浓度下均未观察到与化合物相关的肝细胞增殖速率差异。在1000和5000 ppm时,各种与年龄相关病变的发生率降低。

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