Vladislav E. Sobolev , Richard O. Jenkins , Nikolay V. Goncharov
{"title":"急性暴露于对氧磷和环磷酰胺后大鼠膀胱组织和尿液中的磺化糖胺聚糖","authors":"Vladislav E. Sobolev , Richard O. Jenkins , Nikolay V. Goncharov","doi":"10.1016/j.etp.2017.02.007","DOIUrl":null,"url":null,"abstract":"<div><p><span><span><span>Glycosaminoglycans (GAGs) in the urine of </span>Wistar rats<span><span>, and on the surface of the epithelium and lamina propria of the </span>bladder<span>, were quantitatively assessed before and after acute intoxication with paraoxon or </span></span></span>cyclophosphamide. Paraoxon was administered subcutaneously (s.c.) twice with an interval of 1</span> <!-->h to a final dose of 275<!--> <!-->mg/kg; cyclophosphamide was administered intraperitoneally (i.p.) with a single dose of 100<!--> <!-->mg/kg or to a final dose of 240<!--> <!-->mg/kg (three times per 80<!--> <!-->mg/kg every 12<!--> <span>h). GAGs on the surface of the epithelium and lamina propria of the urinary<span><span> bladder of rats were quantitatively determined by Alcian blue dye staining. GAGs in the urine were determined spectrophotometrically with 1-9-dimethyl </span>methylene blue. By 48–96</span></span> <span><span>h after intoxication with either paraoxon or cyclophosphamide, statistically significant increases in the concentration of GAGs were obtained both for the tissues of the bladder and the urine of rats. Cyclophosphamide, in contrast to paraoxon, caused the development of hemorrhagic cystitis in the animals. The synthesis of GAGs is considered to be compensatory response to the toxic </span>xenobiotics.</span></p></div>","PeriodicalId":50465,"journal":{"name":"Experimental and Toxicologic Pathology","volume":"69 6","pages":"Pages 339-347"},"PeriodicalIF":0.0000,"publicationDate":"2017-07-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.etp.2017.02.007","citationCount":"13","resultStr":"{\"title\":\"Sulfated glycosaminoglycans in bladder tissue and urine of rats after acute exposure to paraoxon and cyclophosphamide\",\"authors\":\"Vladislav E. Sobolev , Richard O. Jenkins , Nikolay V. Goncharov\",\"doi\":\"10.1016/j.etp.2017.02.007\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><span><span><span>Glycosaminoglycans (GAGs) in the urine of </span>Wistar rats<span><span>, and on the surface of the epithelium and lamina propria of the </span>bladder<span>, were quantitatively assessed before and after acute intoxication with paraoxon or </span></span></span>cyclophosphamide. Paraoxon was administered subcutaneously (s.c.) twice with an interval of 1</span> <!-->h to a final dose of 275<!--> <!-->mg/kg; cyclophosphamide was administered intraperitoneally (i.p.) with a single dose of 100<!--> <!-->mg/kg or to a final dose of 240<!--> <!-->mg/kg (three times per 80<!--> <!-->mg/kg every 12<!--> <span>h). GAGs on the surface of the epithelium and lamina propria of the urinary<span><span> bladder of rats were quantitatively determined by Alcian blue dye staining. GAGs in the urine were determined spectrophotometrically with 1-9-dimethyl </span>methylene blue. By 48–96</span></span> <span><span>h after intoxication with either paraoxon or cyclophosphamide, statistically significant increases in the concentration of GAGs were obtained both for the tissues of the bladder and the urine of rats. Cyclophosphamide, in contrast to paraoxon, caused the development of hemorrhagic cystitis in the animals. The synthesis of GAGs is considered to be compensatory response to the toxic </span>xenobiotics.</span></p></div>\",\"PeriodicalId\":50465,\"journal\":{\"name\":\"Experimental and Toxicologic Pathology\",\"volume\":\"69 6\",\"pages\":\"Pages 339-347\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2017-07-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.etp.2017.02.007\",\"citationCount\":\"13\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Experimental and Toxicologic Pathology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0940299316301336\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Experimental and Toxicologic Pathology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0940299316301336","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 13
摘要
定量测定Wistar大鼠急性中毒前后尿液、膀胱上皮和固有层表面的糖胺聚糖(GAGs)含量。对氧磷皮下注射2次,每次间隔1 h,最终剂量为275 mg/kg;腹腔注射环磷酰胺,单次剂量为100 mg/kg或终次剂量为240 mg/kg(每80 mg/kg每12 h 3次)。用阿利新蓝染色法定量测定大鼠膀胱上皮和固有层表面的gag。用1-9-二甲基亚甲基蓝分光光度法测定尿中gag。在对氧磷或环磷酰胺中毒48-96 h后,大鼠膀胱组织和尿液中gag浓度均有统计学意义的升高。环磷酰胺,与对氧磷相反,在动物中引起出血性膀胱炎。GAGs的合成被认为是对有毒外源性药物的代偿反应。
Sulfated glycosaminoglycans in bladder tissue and urine of rats after acute exposure to paraoxon and cyclophosphamide
Glycosaminoglycans (GAGs) in the urine of Wistar rats, and on the surface of the epithelium and lamina propria of the bladder, were quantitatively assessed before and after acute intoxication with paraoxon or cyclophosphamide. Paraoxon was administered subcutaneously (s.c.) twice with an interval of 1 h to a final dose of 275 mg/kg; cyclophosphamide was administered intraperitoneally (i.p.) with a single dose of 100 mg/kg or to a final dose of 240 mg/kg (three times per 80 mg/kg every 12 h). GAGs on the surface of the epithelium and lamina propria of the urinary bladder of rats were quantitatively determined by Alcian blue dye staining. GAGs in the urine were determined spectrophotometrically with 1-9-dimethyl methylene blue. By 48–96h after intoxication with either paraoxon or cyclophosphamide, statistically significant increases in the concentration of GAGs were obtained both for the tissues of the bladder and the urine of rats. Cyclophosphamide, in contrast to paraoxon, caused the development of hemorrhagic cystitis in the animals. The synthesis of GAGs is considered to be compensatory response to the toxic xenobiotics.
期刊介绍:
Cessation. The international multidisciplinary journal is devoted to the publication of studies covering the whole range of experimental research on disease processes and toxicology including cell biological investigations. Its aim is to support progress in the interdisciplinary cooperation of researchers working in pathobiology, toxicology, and cell biology independent of the methods applied. During the past decades increasing attention has been paid to the importance of toxic influence in the pathogenesis of human and animal diseases. This is why Experimental and Toxicologic Pathology meets the urgent need for an interdisciplinary journal felt by a wide variety of experts in medicine and biology, including pathologists, toxicologists, biologists, physicians, veterinary surgeons, pharmacists, and pharmacologists working in academic, industrial or clinical institutions.