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亚慢性给予有机磷酸酯类阻燃剂FYROL 6后大鼠的肝脏变化

Hepatic changes in rats following subchronic administration of FYROL 6, an organophosphorus ester flame retardant.

作者信息

Katz A C, Turnier J C, Zwicker G M, Sprague G L

机构信息

Stauffer Chemical Company, Toxicology Department, Farmington, Connecticut.

出版信息

J Toxicol Environ Health. 1988;23(3):295-301. doi: 10.1080/15287398809531115.

Abstract

This study conducted to evaluate the subchronic toxicity of FYROL 6 [diethyl N,N-bis-(2-hydroxyethyl)aminomethylphosphonate] in rats demonstrated an hepatic effect not commonly reported for related compounds. Sprague-Dawley rats of both sexes were gavaged daily with 0, 10, 100, or 500 mg/kg FYROL 6 in corn oil for 13 wk. No treatment-related mortality and few signs of toxicity were noted during the study. Fyrol 6 did not inhibit plasma, erythrocyte, or brain cholinesterase activities. Treatment-related necropsy and microscopic alterations were restricted to the liver. Increased liver weights, hepatocellular hypertrophy, and eosinophilia of centrilobular hepatocytes were evident in 100-mg/kg females and in both sexes at 500 mg/kg. Morphometric analysis revealed a 40% increase in cross-sectional area of individual hepatocytes in 500-mg/kg males, compared to controls. There was no morphologic evidence of hepatic necrosis or clinical evidence of liver dysfunction. This study demonstrated low toxicity for FYROL 6 and treatment-related changes restricted to the liver suggestive of an adaptive response to FYROL 6.

摘要

本研究旨在评估FYROL 6[二乙基-N,N-双-(2-羟乙基)氨基甲基膦酸酯]对大鼠的亚慢性毒性,结果显示其对肝脏有相关化合物中不常见的影响。将不同性别的斯普拉格-道利大鼠每日经口灌胃给予玉米油中0、10、100或500mg/kg的FYROL 6,持续13周。研究期间未观察到与治疗相关的死亡情况,且几乎没有毒性迹象。FYROL 6未抑制血浆、红细胞或脑胆碱酯酶活性。与治疗相关的尸检和微观改变仅限于肝脏。在100mg/kg的雌性大鼠以及500mg/kg的雌雄大鼠中,肝脏重量增加、肝细胞肥大以及中央小叶肝细胞嗜酸性粒细胞增多均很明显。形态计量分析显示,与对照组相比,500mg/kg雄性大鼠单个肝细胞的横截面积增加了40%。没有肝坏死的形态学证据或肝功能障碍的临床证据。本研究表明FYROL 6毒性较低,且与治疗相关的变化仅限于肝脏,提示对FYROL 6有适应性反应。

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