• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

利用显微解剖技术检测马拉硫磷杂质对肾脏的损害。

Detection of kidney damage by malathion impurities using a microdissection technique.

作者信息

Keadtisuke S, Dheranetra W, Fukuto T R

机构信息

Department of Entomology, University of California, Riverside 92521.

出版信息

Toxicol Lett. 1989 Apr;47(1):53-9. doi: 10.1016/0378-4274(89)90085-4.

DOI:10.1016/0378-4274(89)90085-4
PMID:2652380
Abstract

O,O,S-Trimethylphosphorothioate (OOS-Me) and O,S,S-trimethylphosphorodithioate (OSS-Me) are impurities in technical grade malathion and related insecticides which have been shown to cause delayed death in rats following a single oral dose of 40-60 mg/kg. In connection with studies on the mode of action of these compounds, work on the microdissection and examination of nephrons was carried out. Nephrons from impurities-treated rats showed swelling, distortion and distension of glomeruli, as well as narrowing of the first part of the proximal tubule (swan neck). These results were similar to those observed from kidney tissue obtained from cadmium-chloride-treated rats and are indicative of OOS-Me and OSS-Me-induced kidney tubule damage.

摘要

O,O,S-三甲基硫代磷酸酯(OOS-Me)和O,S,S-三甲基二硫代磷酸酯(OSS-Me)是工业级马拉硫磷及相关杀虫剂中的杂质,已证实大鼠单次口服剂量为40 - 60 mg/kg后会导致延迟死亡。在关于这些化合物作用方式的研究中,开展了肾单位的显微解剖和检查工作。来自用杂质处理过的大鼠的肾单位显示出肾小球肿胀、变形和扩张,以及近端小管起始部分(鹅颈)变窄。这些结果与从氯化镉处理过的大鼠获得的肾组织中观察到的结果相似,表明OOS-Me和OSS-Me会导致肾小管损伤。

相似文献

1
Detection of kidney damage by malathion impurities using a microdissection technique.利用显微解剖技术检测马拉硫磷杂质对肾脏的损害。
Toxicol Lett. 1989 Apr;47(1):53-9. doi: 10.1016/0378-4274(89)90085-4.
2
Liver damage induced in rats by malathion impurities.马拉硫磷杂质对大鼠造成的肝损伤。
Toxicol Lett. 1990 Jun;52(1):35-46. doi: 10.1016/0378-4274(90)90163-g.
3
An impurity of malathion alters the morphology of rat lung bronchiolar epithelium.马拉硫磷的一种杂质会改变大鼠肺细支气管上皮的形态。
Toxicology. 1983 Jan;26(1):73-9. doi: 10.1016/0300-483x(83)90058-6.
4
Lung injury and delayed toxicity produced by O,S,S-trimethyl phosphorodithioate, an impurity of malathion.马拉硫磷的一种杂质O,S,S-三甲基二硫代磷酸酯所导致的肺损伤和迟发性毒性。
Toxicol Appl Pharmacol. 1984 Sep 15;75(2):219-28. doi: 10.1016/0041-008x(84)90204-7.
5
Dysproteinuria induced in rats by O,O,S-trimethyl phosphorothioate.硫代磷酸O,O,S-三甲基酯诱导大鼠产生的异常蛋白尿
Toxicol Lett. 1987 Jun;37(1):33-9. doi: 10.1016/0378-4274(87)90164-0.
6
Phenobarbital pretreatment protects against morphologic changes in rat bronchiolar epithelium caused by an impurity of malathion.苯巴比妥预处理可预防由马拉硫磷杂质引起的大鼠细支气管上皮形态学改变。
Am J Pathol. 1983 Jun;111(3):350-3.
7
Structure and pulmonary toxicity relationship on O,O-dimethyl S-alkyl phosphorothioate esters.O,O-二甲基-S-烷基硫代磷酸酯的结构与肺毒性关系
Pharmacol Toxicol. 1990 May;66(5):367-72. doi: 10.1111/j.1600-0773.1990.tb00764.x.
8
Role of metabolic activation, covalent binding, and glutathione depletion in pulmonary toxicity produced by an impurity of malathion.代谢活化、共价结合和谷胱甘肽耗竭在马拉硫磷一种杂质所致肺部毒性中的作用。
Toxicol Appl Pharmacol. 1984 Mar 15;72(3):476-83. doi: 10.1016/0041-008x(84)90124-8.
9
Malathion and phenthoate carboxylesterase activities in pulmonary alveolar macrophages as indicators of lung injury.
Toxicol Appl Pharmacol. 1983 Aug;70(1):140-7. doi: 10.1016/0041-008x(83)90187-4.
10
Neonatal death and lung injury in rats caused by intrauterine exposure to O,O,S-trimethylphosphorothioate.宫内暴露于O,O,S-三甲基硫代磷酸酯导致的新生大鼠死亡和肺损伤。
Arch Toxicol. 1988 Apr;61(5):378-86. doi: 10.1007/BF00334619.

引用本文的文献

1
Molecular Mechanisms of Acute Organophosphate Nephrotoxicity.急性有机磷肾病的分子机制。
Int J Mol Sci. 2022 Aug 9;23(16):8855. doi: 10.3390/ijms23168855.
2
Nephrotic syndrome and acute kidney injury induced by malathion toxicity.马拉硫磷中毒所致肾病综合征和急性肾损伤
BMJ Case Rep. 2017 Nov 9;2017:bcr-2017-220733. doi: 10.1136/bcr-2017-220733.