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恒河猴(猕猴)中2,3,4,7,8-五氯二苯并呋喃(4PeCDF)的毒性与处置情况

Toxicity and disposition of 2,3,4,7,8-pentachlorodibenzofuran (4PeCDF) in the rhesus monkey (Macaca mulatta).

作者信息

Brewster D W, Elwell M R, Birnbaum L S

机构信息

Systemic Toxicology Branch, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27707.

出版信息

Toxicol Appl Pharmacol. 1988 Apr;93(2):231-46. doi: 10.1016/0041-008x(88)90123-8.

Abstract

The toxicity and disposition of 2,3,4,7,8-pentachlorodibenzofuran (4PeCDF), a ubiquitous and acutely toxic environmental contaminant, was examined in three adult male Rhesus monkeys administered a single iv dose of 34 micrograms (0.1 mumol)/kg. Within 20 min, 4PeCDF was eliminated from the blood and was distributed to the liver, skin, adipose, and muscle tissues. Excretion occurred primarily via the feces with a minimum whole body half-life approximately 38 days. Within 7-14 days after administration, the packed cell volume and serum triglyceride and bile acid concentrations were significantly increased while serum cholesterol, protein, and albumin concentrations were decreased relative to pretreatment levels. Thyroid hormone levels were also altered with an increase in TSH and a decrease in T3 and T4 concentrations. After 28 days, two monkeys began exhibiting alopecia, hyperkeratinization of the toe and finger nails, facial chloracne-like lesions, and loss of body weight. They subsequently died 40 and 48 days after treatment. Similar symptoms of toxicity were observed in the third animal 58 days after 4PeCDF administration, but this animal appeared to fully recover and was administered 4PeCDF orally and [3H]1,2,3,7,8-pentachloro-dibenzofuran (1PeCDF) dermally 238 days after the initial iv dose. In this animal, approximately 2% of an oral dose of [14C]-4PeCDF was absorbed from the stomach and small intestine in 6 hr and was distributed mainly to the muscle and skin and less than 99% of a dermal dose of 1PeCDF remained at the site of application. Pathological findings in the monkeys that died indicated hyperplastic and metaplastic changes in the gastric mucosa, the Meibomian glands of the eyelid, and the ceruminous glands of the ear. Regression of these lesions was present in the surviving animal. Therefore, 4PeCDF produces dioxin-like toxicity in the monkey similar to that reported for 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) and in the same dose range.

摘要

2,3,4,7,8 - 五氯二苯并呋喃(4PeCDF)是一种普遍存在且具有急性毒性的环境污染物,对三只成年雄性恒河猴进行研究,静脉注射单次剂量34微克(0.1微摩尔)/千克,以此检测其毒性和处置情况。给药后20分钟内,4PeCDF从血液中清除,并分布至肝脏、皮肤、脂肪和肌肉组织。排泄主要通过粪便进行,全身最小半衰期约为38天。给药后7 - 14天内,相对于给药前水平,红细胞压积、血清甘油三酯和胆汁酸浓度显著升高,而血清胆固醇、蛋白质和白蛋白浓度降低。甲状腺激素水平也发生改变,促甲状腺激素升高,T3和T4浓度降低。28天后,两只猴子开始出现脱发、趾甲和指甲过度角化、面部类似氯痤疮的病变以及体重减轻。它们随后在治疗后40天和48天死亡。在4PeCDF给药58天后,第三只动物也观察到类似的毒性症状,但这只动物似乎完全康复,并在首次静脉注射剂量238天后口服4PeCDF和经皮给予[3H] - 1,2,3,7,8 - 五氯二苯并呋喃(1PeCDF)。在这只动物中,口服剂量的[14C] - 4PeCDF约2%在6小时内从胃和小肠吸收,主要分布至肌肉和皮肤,经皮给予的1PeCDF剂量中不到99%保留在给药部位。死亡猴子的病理检查结果显示胃黏膜、眼睑睑板腺和耳耵聍腺出现增生和化生改变。存活动物中这些病变有所消退。因此,4PeCDF在猴子中产生的二噁英样毒性与2,3,7,8 - 四氯二苯并 - p - 二噁英(TCDD)报道的相似,且在相同剂量范围内。

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