{"title":"异氟醚加重过氧化氢诱导肺泡II型细胞磷脂酰胆碱合成的减少","authors":"T. Yang, Y. Li, Q. Liu, Jun Tao, W. Wu, H. Huang,","doi":"10.1515/DMDI.2001.18.3-4.243","DOIUrl":null,"url":null,"abstract":"The influence of isoflurane (Iso) on the synthesis and secretion of phosphatidylcholine (PC) of alveolar type II cells (AT II cells) injured by hydrogen peroxide (H2O2) was investigated. After primary culturing for 32 h, AT II cells isolated and purified from adult Sprague-Dawley rats were randomly divided into six groups: control group, 02.8 mM Iso group, 2.8 mM Iso group, 75 microM H2O2 group, 75 microM H2O2 + 0.28 mM Iso group, and 75 microM H202 + 2.8 mM Iso group. Synthesis and secretion of phosphatidylcholine (PC) were detected by 3H-choline chloride incorporation. It was found that 0.28 mM and 2.8 mM Iso significantly reduced PC synthesis compared with the control group (p <0.05, p <0.01, respectively), but not PC secretion. 75 microM H2O2 markedly decreased the synthesis and secretion of PC in AT II cells compared with the control group (p <0.01). 0.28 mM and 2.8 mM Iso aggravated the decrease of PC synthesis induced by H2O2 (p <0.05, p <0.01, respectively), but did not affect PC secretion. These findings suggest that Iso itself may inhibit the synthesis of PC of AT II cells in vitro and further damage the cells' function under peroxidation.","PeriodicalId":77889,"journal":{"name":"Reviews on drug metabolism and drug interactions","volume":"18 1","pages":"243 - 250"},"PeriodicalIF":0.0000,"publicationDate":"2001-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1515/DMDI.2001.18.3-4.243","citationCount":"5","resultStr":"{\"title\":\"Isoflurane Aggravates the Decrease of Phosphatidycholine Synthesis in Alveolar Type II Cells Induced by Hydrogen Peroxide\",\"authors\":\"T. Yang, Y. Li, Q. Liu, Jun Tao, W. Wu, H. Huang,\",\"doi\":\"10.1515/DMDI.2001.18.3-4.243\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The influence of isoflurane (Iso) on the synthesis and secretion of phosphatidylcholine (PC) of alveolar type II cells (AT II cells) injured by hydrogen peroxide (H2O2) was investigated. After primary culturing for 32 h, AT II cells isolated and purified from adult Sprague-Dawley rats were randomly divided into six groups: control group, 02.8 mM Iso group, 2.8 mM Iso group, 75 microM H2O2 group, 75 microM H2O2 + 0.28 mM Iso group, and 75 microM H202 + 2.8 mM Iso group. Synthesis and secretion of phosphatidylcholine (PC) were detected by 3H-choline chloride incorporation. It was found that 0.28 mM and 2.8 mM Iso significantly reduced PC synthesis compared with the control group (p <0.05, p <0.01, respectively), but not PC secretion. 75 microM H2O2 markedly decreased the synthesis and secretion of PC in AT II cells compared with the control group (p <0.01). 0.28 mM and 2.8 mM Iso aggravated the decrease of PC synthesis induced by H2O2 (p <0.05, p <0.01, respectively), but did not affect PC secretion. These findings suggest that Iso itself may inhibit the synthesis of PC of AT II cells in vitro and further damage the cells' function under peroxidation.\",\"PeriodicalId\":77889,\"journal\":{\"name\":\"Reviews on drug metabolism and drug interactions\",\"volume\":\"18 1\",\"pages\":\"243 - 250\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2001-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1515/DMDI.2001.18.3-4.243\",\"citationCount\":\"5\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Reviews on drug metabolism and drug interactions\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1515/DMDI.2001.18.3-4.243\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Reviews on drug metabolism and drug interactions","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1515/DMDI.2001.18.3-4.243","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 5
摘要
研究了异氟醚(Iso)对过氧化氢(H2O2)损伤肺泡II型细胞(AT II细胞)磷脂酰胆碱(PC)合成和分泌的影响。原代培养32 h后,取成年sd大鼠分离纯化的AT II细胞,随机分为6组:对照组、02.8 mM Iso组、2.8 mM Iso组、75 microM H2O2组、75 microM H2O2 + 0.28 mM Iso组和75 microM H202 + 2.8 mM Iso组。采用3h -氯化胆碱法检测磷脂酰胆碱(PC)的合成和分泌。结果表明,与对照组相比,0.28 mM和2.8 mM Iso显著降低了PC合成(p <0.05, p <0.01),但对PC分泌无显著影响。与对照组相比,75 μ m H2O2显著降低了AT II细胞PC的合成和分泌(p <0.01)。0.28 mM和2.8 mM Iso加重H2O2诱导的PC合成减少(p <0.05, p <0.01),但不影响PC分泌。这些结果表明,Iso本身可能在体外抑制AT II细胞的PC合成,进一步损害细胞在过氧化作用下的功能。
Isoflurane Aggravates the Decrease of Phosphatidycholine Synthesis in Alveolar Type II Cells Induced by Hydrogen Peroxide
The influence of isoflurane (Iso) on the synthesis and secretion of phosphatidylcholine (PC) of alveolar type II cells (AT II cells) injured by hydrogen peroxide (H2O2) was investigated. After primary culturing for 32 h, AT II cells isolated and purified from adult Sprague-Dawley rats were randomly divided into six groups: control group, 02.8 mM Iso group, 2.8 mM Iso group, 75 microM H2O2 group, 75 microM H2O2 + 0.28 mM Iso group, and 75 microM H202 + 2.8 mM Iso group. Synthesis and secretion of phosphatidylcholine (PC) were detected by 3H-choline chloride incorporation. It was found that 0.28 mM and 2.8 mM Iso significantly reduced PC synthesis compared with the control group (p <0.05, p <0.01, respectively), but not PC secretion. 75 microM H2O2 markedly decreased the synthesis and secretion of PC in AT II cells compared with the control group (p <0.01). 0.28 mM and 2.8 mM Iso aggravated the decrease of PC synthesis induced by H2O2 (p <0.05, p <0.01, respectively), but did not affect PC secretion. These findings suggest that Iso itself may inhibit the synthesis of PC of AT II cells in vitro and further damage the cells' function under peroxidation.