Subacute oral toxicity of 1,4-butanediol in rats.

R A Jedrychowski, R Górny, J Stetkiewicz, I Stetkiewicz
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Abstract

1,4-Butanediol (BAD) was administered to male and female Wistar Imp:DAK rats by oral gavage for 28 consecutive days. Treated rats received BAD at daily doses of 5, 50 or 500 mg/kg/day. After 28 days all animals were necropsied. Blood samples were obtained and selected organs were weighed and prepared for histological examination. Subacute oral administration of BAD resulted in an overall low degree of systemic toxicity. There were no changes in body weight, food consumption, and absolute and relative organ weights. Slightly higher activities of sorbitol dehydrogenase and alanine aminotransferase were observed in male rats given BAD at the highest dose of 500 mg/kg/day. Some disturbances in hematological parameters, characterized by macrocytosis and thrombocytopenia were observed in treated rats. Mild to moderate inflammation of the liver, characterized by proliferation of bile ducts and periportal infiltrations with fibroblasts and mononuclear cells, were found in treated animals. A statistically significant difference for histopathological changes was found in animals treated with BAD at the dose of 500 mg/kg/day only in the case where both sexes were jointly taken for comparison.

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1,4-丁二醇对大鼠的亚急性口服毒性。
用1,4-丁二醇(BAD)灌胃Wistar Imp:DAK雄性和雌性大鼠,连续28天。接受BAD治疗的大鼠每日剂量分别为5、50或500 mg/kg/天。28天后对所有动物进行尸检。采集血样,对选定的器官称重,准备进行组织学检查。亚急性口服BAD导致整体低程度的全身毒性。体重、食物消耗量、绝对和相对器官重量没有变化。雄性大鼠在最高剂量500mg /kg/d时山梨醇脱氢酶和丙氨酸转氨酶活性略高。治疗后大鼠血液学参数出现一些紊乱,表现为巨噬细胞增多和血小板减少。在治疗动物中发现轻度至中度肝脏炎症,其特征是胆管增生和成纤维细胞和单核细胞浸润门静脉周围。500mg /kg/天BAD剂量组的组织病理学变化有统计学上的显著差异,仅在两性联合服用BAD进行比较的情况下。
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