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茶碱诱导F344/N大鼠肠系膜动脉周围炎

Theophylline-induced mesenteric periarteritis in F344/N rats.

作者信息

Nyska A, Herbert R A, Chan P C, Haseman J K, Hailey J R

机构信息

Environmental Toxicology Program, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA.

出版信息

Arch Toxicol. 1998 Nov;72(11):731-7. doi: 10.1007/s002040050567.

Abstract

The toxicity and carcinogenic potential of theophylline (an alkaloid bronchodilator drug) was investigated in male and female F344/N rats in 16-day, 14-week, and 2-year gavage and feeding studies. In 16-day studies, rats were fed diets containing 0, 500, 1000, 2000, 4000, and 8000 ppm of theophylline or given 0, 12.5 (twice daily), 25 (once daily), 50 (once daily), 50 (twice daily), 100 (once daily), 200 (once daily), 200 (twice daily), and 400 (once daily) mg theophylline/kg body weight in corn oil by gavage. In 14-week studies, rats were fed diets containing 0, 1000, 2000, and 4000 ppm theophylline or given 0, 37.5, 75, and 150 mg/kg body weight theophylline in corn oil by gavage. In 2-year gavage studies, rats were given 0, 7.5, 25, and 75 mg/kg body weight in corn oil. In 16-day gavage studies, treatment-related periarteritis occurred in arteries of the pancreas and adjacent to the mesenteric lymph nodes of early death male and female rats given 400 mg/kg once daily. In the 14-week studies, treatment-related periarteritis occurred at similar sites and in male rats exposed to 75 and 150 mg/kg, and in all exposed female rats (gavage studies), in females exposed to 1000 ppm, and in both sexes exposed to 2000 and 4000 ppm (feeding studies). In the 2-year study, chronic periarteritis was significantly increased only in the males receiving 75 mg/kg of theophylline. The adventitia, media and intima of medium- and large-sized mesenteric arteries were involved. Similar to other vasodilator chemicals, the pathogenesis of theophylline-induced vascular lesions may be a consequence of hemodynamic changes induced in the vascular wall.

摘要

在雄性和雌性F344/N大鼠中,通过16天、14周和2年的灌胃及喂养研究,对茶碱(一种生物碱支气管扩张药物)的毒性和致癌潜力进行了调查。在16天的研究中,给大鼠喂食含0、500、1000、2000、4000和8000 ppm茶碱的饲料,或通过灌胃给予玉米油中0、12.5(每日两次)、25(每日一次)、50(每日一次)、50(每日两次)、100(每日一次)、200(每日一次)、200(每日两次)和400(每日一次)mg/kg体重的茶碱。在14周的研究中,给大鼠喂食含0、1000、2000和4000 ppm茶碱的饲料,或通过灌胃给予玉米油中0、37.5、75和150 mg/kg体重的茶碱。在2年的灌胃研究中,给大鼠玉米油中0、7.5、25和75 mg/kg体重的茶碱。在16天的灌胃研究中,每日一次给予400 mg/kg的早期死亡雄性和雌性大鼠,在胰腺动脉以及肠系膜淋巴结附近出现与治疗相关的动脉周围炎。在14周的研究中,在类似部位出现与治疗相关的动脉周围炎,在暴露于75和150 mg/kg的雄性大鼠以及所有暴露的雌性大鼠中(灌胃研究),在暴露于1000 ppm的雌性大鼠中,以及在暴露于2000和4000 ppm的两性大鼠中(喂养研究)。在2年的研究中,仅在接受75 mg/kg茶碱的雄性大鼠中,慢性动脉周围炎显著增加。中、大型肠系膜动脉的外膜、中膜和内膜均受累。与其他血管扩张剂化学物质类似,茶碱诱导的血管病变的发病机制可能是血管壁中血流动力学变化的结果。

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