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洗涤剂配方螯合剂对小鼠体内镉代谢及毒性的影响。

Effects of detergent formula chelating agents on the metabolism and toxicity of cadmium in mice.

作者信息

Engström B, Nordberg G F

出版信息

Acta Pharmacol Toxicol (Copenh). 1978 Nov;43(5):387-97. doi: 10.1111/j.1600-0773.1978.tb02283.x.

Abstract

Chelating agents like NTA (nitrilotriacetic acid) STPP (sodiumtripolyphosphate, Na5P3O10) and EDTA (ethylenediaminetetraacetic acid) are used as components of detergents. An increased toxicity of some metal compounds when combined with NTA has led to decreased use of this chelating agent in relation to STPP. In the present studies short-term and long-term effects of these chelating agents on cadmium toxicity in mice were investigated. I: In the short-term study, mice subcutaneously exposed to CdCl2 (3.2 mg Cd/kg b. wt.) in combination with STPP (32 mg/kg b. wt.) demonstrated a markedly higher mortality compared to animals given CdCl2 alone. This increase in mortality was similar to the one encountered when CdCl2 (3.2 mg Cd/kg b. wt.) and NTA (32 mg/kg b. wt.) were combined. Animals exposed subcutaneously to CdCl2 + STPP or CdCl2 + NTA showed histological evidence of liver necrosis 24 hrs after exposure not seen in animals given the same dose of CdCl2 alone and also had markedly lower cadmium concentrations in the livers compared to only Cd-exposed animals. II: In the long-term study, mice were exposed orally to CdSO4 (50p.p.m Cd) alone or in combination with STPP (500 p.p.m.), NTA (500 p.p.m.) or EDTA (50 p.p.m.) by continuous administration via the drinking water for 18 months. A decreased total excretion of urine proteins was seen in all Cd-treated animals irrespectively of the combination with various chelating agents. The conclusion of the present work was the NTA and STPP given by subcutaneous injection to mice markedly increased the toxicity of cadmium but that neither NTA, STPP nor EDTA given orally altered the toxicity of cadmium during a period of long-term exposure of 18 months.

摘要

螯合剂如氮川三乙酸(NTA)、三聚磷酸钠(STPP,Na5P3O10)和乙二胺四乙酸(EDTA)被用作洗涤剂的成分。一些金属化合物与NTA结合时毒性增加,导致该螯合剂相对于STPP的使用减少。在本研究中,研究了这些螯合剂对小鼠镉毒性的短期和长期影响。一、短期研究:皮下注射氯化镉(3.2毫克镉/千克体重)与STPP(32毫克/千克体重)的小鼠,与单独给予氯化镉的动物相比,死亡率显著更高。这种死亡率的增加与氯化镉(3.2毫克镉/千克体重)和NTA(32毫克/千克体重)联合使用时的情况相似。皮下注射氯化镉+STPP或氯化镉+NTA的动物在接触24小时后出现肝坏死的组织学证据,而单独给予相同剂量氯化镉的动物未见此现象,并且与仅接触镉的动物相比,其肝脏中的镉浓度也显著降低。二、长期研究:小鼠通过饮用水连续给药18个月,口服硫酸镉(50 ppm镉),单独或与STPP(500 ppm)、NTA(500 ppm)或EDTA(50 ppm)联合使用。无论与各种螯合剂如何组合,所有镉处理的动物尿液蛋白总排泄量均减少。本研究的结论是,皮下注射给小鼠的NTA和STPP显著增加了镉的毒性,但在18个月的长期暴露期间,口服给予的NTA、STPP或EDTA均未改变镉的毒性。

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