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增塑剂邻苯二甲酸二(2-乙基己基)酯对大鼠影响的时间和剂量反应研究

Time and dose-response study of the effects on rats of the plasticizer di(2-ethylhexyl) phthalate.

作者信息

Mitchell F E, Price S C, Hinton R H, Grasso P, Bridges J W

出版信息

Toxicol Appl Pharmacol. 1985 Dec;81(3 Pt 1):371-92. doi: 10.1016/0041-008x(85)90409-0.

Abstract

Groups of male and groups of female Wistar albino rats were administered diets containing sufficient di(2-ethylhexyl) phthalate (DEHP) to ensure intakes of either 1000, 200, or 50 mg/kg/day. Four rats from each experimental group and six control rats of the same sex were killed 3, 7, 14, and 28 days and 9 months after commencement of treatment. At all time points the major abdominal organs were removed and subjected to histological examination. A more extensive necropsy was performed on those rats killed after 9 months of treatment. At all time points the livers of the rats were subjected to extensive histologic, electron microscopic, and biochemical examination. Changes could be grouped according to their time course. Two early and transient alterations were noticed. First, there were morphologic changes in the bile canaliculi of male rats treated with 1000 mg/kg/day of DEHP. Second, there was a burst of mitosis immediately after the start of administration of the compound. The time course of this mitotic burst varied; the increase in mitosis was greatest at 3 days in rats treated with 1000 mg/kg/day of DEHP and was smaller but more prolonged in rats treated with 200 or 50 mg/kg/day. Other changes, namely, a midzonal to periportal accumulation of fat, induction of peroxisomal enzymes, and induction of the P-450 isoenzyme also developed rapidly but were sustained throughout the study. The maximal change was usually attained within 7 days of commencement of treatment. More slowly developing changes were hypertrophy of the hepatocytes, centrilobular loss of glycogen, and a fall in glucose-6-phosphatase activity. Here maximal changes were not attained until 28 days after commencement of treatment. These three effects were clearly observed in rats treated with 200 or 1000 mg/kg/day of DEHP but were only marginally altered in rats treated with 50 mg/kg/day. Finally accumulation of lipid-loaded lysosomes assessed by light and electron microscopy and by assay of beta-galactosidase activity was only apparent in rats treated with DEHP for 9 months with 200 or 1000 mg/kg/day of DEHP. Changes in female rats were qualitatively similar to those observed in male rats. The alterations were, however, less pronounced than in male rats treated with an equal dose of DEHP and the degree of liver enlargement was much less because, although the initial hyperplasia was clearly apparent, there was a much smaller degree of hypertrophy.

摘要

将雄性和雌性Wistar白化大鼠分为不同组,分别给予含有足够邻苯二甲酸二(2-乙基己基)酯(DEHP)的饮食,以确保摄入量分别为1000、200或50毫克/千克/天。在治疗开始后的3、7、14、28天以及9个月,处死每组实验大鼠中的4只以及相同性别的6只对照大鼠。在所有时间点,取出主要腹部器官并进行组织学检查。对治疗9个月后处死的大鼠进行了更全面的尸检。在所有时间点,对大鼠的肝脏进行了广泛的组织学、电子显微镜和生化检查。这些变化可根据其时间进程进行分类。发现了两种早期且短暂的改变。首先,给予1000毫克/千克/天DEHP的雄性大鼠胆小管出现形态学变化。其次,在给予该化合物后立即出现有丝分裂爆发。这种有丝分裂爆发的时间进程各不相同;给予1000毫克/千克/天DEHP的大鼠在第3天有丝分裂增加最为明显,而给予200或50毫克/千克/天的大鼠有丝分裂增加较小但持续时间更长。其他变化,即中区至门周脂肪堆积、过氧化物酶体酶诱导以及P-450同工酶诱导也迅速出现,但在整个研究过程中持续存在。最大变化通常在治疗开始后7天内达到。发展较为缓慢的变化是肝细胞肥大、中央小叶糖原丢失以及葡萄糖-6-磷酸酶活性下降。这里最大变化直到治疗开始后28天才达到。在给予200或1000毫克/千克/天DEHP的大鼠中清楚地观察到了这三种效应,但在给予50毫克/千克/天的大鼠中仅有轻微改变。最后,通过光学和电子显微镜以及β-半乳糖苷酶活性测定评估的脂质负载溶酶体的积累仅在给予200或1000毫克/千克/天DEHP处理9个月的大鼠中明显。雌性大鼠的变化在性质上与雄性大鼠观察到的变化相似。然而,这些改变不如给予同等剂量DEHP的雄性大鼠明显,肝脏肿大程度也小得多,因为尽管最初的增生明显,但肥大程度要小得多。

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