{"title":"NG-Hydroxy-L-Arginine Releases from Endothelial Cells Nitric Oxide which Increases cGMP in RFL-6 Fibroblasts","authors":"T. Swierkosz, T. Warner, J. Vane","doi":"10.3109/10623329509053388","DOIUrl":null,"url":null,"abstract":"The release of nitric oxide (NO) by NG-hydroxy-L-arginine (L-OHArg) from endothelial cells (ECs) grown in culture was assessed by two bioassays. The first was a cascade bioassay system, in which the effluent from a column of ECs grown on beads superfused a cascade of isolated endothelium-denuded rabbit aortic strips. Exclusion of calcium from the Krebs' buffer perfusing the ECs (but not from the cascade) diminished the relaxant effects of L-OHArg. Growing the ECs in the presence of dexamethasone did not affect the relaxations of the bioassay cascade induced by L-OHArg. However, these relaxations were potentiated by superoxide dismutase (SOD) and inhibited by haemoglobin, but not inhibited by NG-nitro-L-arginine methyl ester (NO2 ArgMeE). The second bioassay was a transfer assay, in which accumulation of cGMP was measured in detector, RFL-6 fibroblast cells. The accumulation of cGMP induced by the basal release of NO from ECs was increased by L-OHArg and by SOD. However, L-OHArg, unlike SOD, did not scaven...","PeriodicalId":11588,"journal":{"name":"Endothelium-journal of Endothelial Cell Research","volume":"4 1","pages":"121-129"},"PeriodicalIF":0.0000,"publicationDate":"1995-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Endothelium-journal of Endothelial Cell Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3109/10623329509053388","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
The release of nitric oxide (NO) by NG-hydroxy-L-arginine (L-OHArg) from endothelial cells (ECs) grown in culture was assessed by two bioassays. The first was a cascade bioassay system, in which the effluent from a column of ECs grown on beads superfused a cascade of isolated endothelium-denuded rabbit aortic strips. Exclusion of calcium from the Krebs' buffer perfusing the ECs (but not from the cascade) diminished the relaxant effects of L-OHArg. Growing the ECs in the presence of dexamethasone did not affect the relaxations of the bioassay cascade induced by L-OHArg. However, these relaxations were potentiated by superoxide dismutase (SOD) and inhibited by haemoglobin, but not inhibited by NG-nitro-L-arginine methyl ester (NO2 ArgMeE). The second bioassay was a transfer assay, in which accumulation of cGMP was measured in detector, RFL-6 fibroblast cells. The accumulation of cGMP induced by the basal release of NO from ECs was increased by L-OHArg and by SOD. However, L-OHArg, unlike SOD, did not scaven...
通过两种生物测定法评估ng -羟基- l -精氨酸(L-OHArg)对内皮细胞(ECs)释放一氧化氮(NO)的影响。第一个是级联生物测定系统,其中从珠子上生长的内皮细胞柱流出的废水与分离的内皮剥离的兔主动脉条带级联。从灌注ECs的克雷伯缓冲液中排除钙(而不是从级联中排除钙)会减弱L-OHArg的松弛作用。在地塞米松存在下生长的ECs不影响L-OHArg诱导的生物测定级联的松弛。然而,这些松弛被超氧化物歧化酶(SOD)增强,被血红蛋白抑制,但不被ng -硝基- l -精氨酸甲酯(NO2 ArgMeE)抑制。第二个生物试验是转移试验,在检测RFL-6成纤维细胞中测量cGMP的积累。L-OHArg和SOD增加了ECs基础释放NO诱导的cGMP积累。然而,与SOD不同,L-OHArg不清除…