{"title":"雄性Wistar白化大鼠体内丙烯酸甲酯的配置和代谢。","authors":"A Sapota","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>The present study was designed to investigate methyl-[2,3-14C]acrylate (MA) distribution, excretion, and metabolism. Data presented here show that the radioactivity derived from MA is rapidly absorbed after i.p. and p.o. administration and distributed into all major tissues of rats. The highest concentration of MA-derived radioactivity was detected mainly in the liver and kidneys at 1 (i.p.) or 2 (p.o.) hours after dosing. There were only slight differences observed in the dynamics of tissue distribution and excretion in relation to the route of administration. The major route of MA excretion was CO2 exhalation (approximately 54% of the administered dose in 48 h) followed by urinary excretion. Two metabolites were identified in the urine, namely, N-acetyl-S-(2-methylcarboxyethyl)cysteine and N-acetyl-S-(2-carboxyethyl)cysteine, and ratio between those was about 1:1.</p>","PeriodicalId":20359,"journal":{"name":"Polish journal of occupational medicine and environmental health","volume":"6 2","pages":"185-93"},"PeriodicalIF":0.0000,"publicationDate":"1993-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The disposition and metabolism of methyl acrylate in male Wistar albino rats.\",\"authors\":\"A Sapota\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The present study was designed to investigate methyl-[2,3-14C]acrylate (MA) distribution, excretion, and metabolism. Data presented here show that the radioactivity derived from MA is rapidly absorbed after i.p. and p.o. administration and distributed into all major tissues of rats. The highest concentration of MA-derived radioactivity was detected mainly in the liver and kidneys at 1 (i.p.) or 2 (p.o.) hours after dosing. There were only slight differences observed in the dynamics of tissue distribution and excretion in relation to the route of administration. The major route of MA excretion was CO2 exhalation (approximately 54% of the administered dose in 48 h) followed by urinary excretion. Two metabolites were identified in the urine, namely, N-acetyl-S-(2-methylcarboxyethyl)cysteine and N-acetyl-S-(2-carboxyethyl)cysteine, and ratio between those was about 1:1.</p>\",\"PeriodicalId\":20359,\"journal\":{\"name\":\"Polish journal of occupational medicine and environmental health\",\"volume\":\"6 2\",\"pages\":\"185-93\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1993-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Polish journal of occupational medicine and environmental health\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Polish journal of occupational medicine and environmental health","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
本研究旨在研究甲基-[2,3- 14c]丙烯酸酯(MA)的分布、排泄和代谢。本研究的数据表明,MA的放射性在给药后迅速被吸收,并分布到大鼠的所有主要组织中。在给药后1(1个小时)或2(1个小时),主要在肝脏和肾脏检测到最高浓度的ma衍生放射性。与给药途径有关的组织分布和排泄动力学仅观察到轻微的差异。MA的主要排泄途径是CO2呼出(约占48小时给药剂量的54%),其次是尿排泄。在尿中鉴定出两种代谢物,即n -乙酰- s -(2-甲基羧乙基)半胱氨酸和n -乙酰- s -(2-羧乙基)半胱氨酸,两者的比例约为1:1。
The disposition and metabolism of methyl acrylate in male Wistar albino rats.
The present study was designed to investigate methyl-[2,3-14C]acrylate (MA) distribution, excretion, and metabolism. Data presented here show that the radioactivity derived from MA is rapidly absorbed after i.p. and p.o. administration and distributed into all major tissues of rats. The highest concentration of MA-derived radioactivity was detected mainly in the liver and kidneys at 1 (i.p.) or 2 (p.o.) hours after dosing. There were only slight differences observed in the dynamics of tissue distribution and excretion in relation to the route of administration. The major route of MA excretion was CO2 exhalation (approximately 54% of the administered dose in 48 h) followed by urinary excretion. Two metabolites were identified in the urine, namely, N-acetyl-S-(2-methylcarboxyethyl)cysteine and N-acetyl-S-(2-carboxyethyl)cysteine, and ratio between those was about 1:1.