Dodd D E, Snellings W M, Maronpot R R, Ballantyne B
Toxicol Appl Pharmacol. 1983 May;68(3):405-14. doi: 10.1016/0041-008x(83)90285-5.
The acute 4-hr LC50 (with 95% confidence limits) for Fischer 344 rats was determined to be 486 (339 to 696) ppm of ethylene glycol monobutyl ether (EGBE) for males and 450 (315 to 645) ppm for females. Notable observations included loss of coordination, red stained urine, and enlarged discolored kidneys at 867 and 523 ppm. In a subsequent study, rats were exposed for 9 days (6 hr/day) to EGBE concentrations of 245, 86, 20, or 0 (control) ppm. There were significant depressions of red blood cell (RBC) count (approximately 20% below control values), hemoglobin (Hgb), and mean corpuscular hemoglobin (MCH) concentration and increases in nucleated erythrocytes, reticulocytes, and lymphocytes in males and females of the 245 ppm group. Decreased body weight gains and increased liver weights were also found. A 14-day postexposure recovery showed substantial reversal of the affected blood parameters. Similar, but less marked, hematologic effects were observed in rats exposed to 86 ppm of EGBE, while rats of the 20 ppm group were indistinguishable from controls. In a 90-day study, rats were exposed to EGBE concentrations of 77, 25, 5, or 0 ppm for 13 weeks (6 hr/day, 5 days/week). Slight, but statistically significant, decreases in RBC (13% below control) and Hgb, accompanied by an increase in MCH (11% above control) were observed in the 77 ppm-exposed females after 6 weeks. At the conclusion of the 90-day exposure regimen, the hematologic effects seen in the females had lessened (RBC was 7% below control) or returned to control value ranges. Furthermore, no treatment-related differences were found in body weight, organ weights, urine or serum chemistries, gross lesions, or microscopic lesions in males or females. There were no significant biological effects in rats exposed subchronically to 25 or 5 ppm. The subtle hematologic findings of these studies confirm the known RBC perturbations of EGBE.
经测定,费希尔344大鼠的急性4小时半数致死浓度(LC50,含95%置信区间)为:雄性大鼠的乙二醇单丁醚(EGBE)为486(339至696)ppm,雌性大鼠为450(315至645)ppm。显著观察结果包括:在867 ppm和523 ppm浓度下,大鼠出现协调能力丧失、尿液染红以及肾脏肿大变色。在随后的一项研究中,大鼠连续9天(每天6小时)暴露于浓度为245、86、20或0(对照)ppm的EGBE环境中。在245 ppm组的雄性和雌性大鼠中,红细胞(RBC)计数(比对照值低约20%)、血红蛋白(Hgb)和平均红细胞血红蛋白(MCH)浓度均显著降低,有核红细胞、网织红细胞和淋巴细胞数量增加。还发现体重增加减少和肝脏重量增加。暴露后14天的恢复情况显示,受影响的血液参数有显著逆转。在暴露于86 ppm EGBE的大鼠中观察到类似但不太明显的血液学效应,而20 ppm组的大鼠与对照组无明显差异。在一项为期90天的研究中,大鼠连续13周(每天6小时,每周5天)暴露于浓度为77、25、5或0 ppm的EGBE环境中。6周后,在暴露于77 ppm的雌性大鼠中,观察到RBC(比对照低13%)和Hgb略有下降,但具有统计学意义,同时MCH增加(比对照高11%)。在90天暴露方案结束时,雌性大鼠中观察到的血液学效应有所减轻(RBC比对照低7%)或恢复到对照值范围。此外,在雄性或雌性大鼠的体重、器官重量、尿液或血清化学、大体病变或微观病变方面,未发现与治疗相关差异。在亚慢性暴露于25 ppm或5 ppm的大鼠中未观察到显著生物学效应。这些研究中细微的血液学发现证实了EGBE已知的对红细胞的干扰作用。