{"title":"过氧化物(ONOO-)对人红细胞(hRBC)氧化损伤的调节作用","authors":"A. Bala, P. Haldar","doi":"10.14800/ICS.695","DOIUrl":null,"url":null,"abstract":"Monitoring of oxidative stress to human red blood cells (hRBC) is scientifically important for any kind of disease etiology or even during of any drug therapies however the comparative toxicity of reactive species in hRBC in term of hemolysis was not yet established. In this context the present study highlighted the different oxidative assay induced either by superoxide (O 2 - )or by hydrogen peroxide (H 2 O 2 )or by nitric oxide (NO) or by peroxinitrite (ONOO - )using different biochemical reactions in isolated hRBC cells. The oxidative hemolysis was significantly ( p 0.05). The induction of oxidative stress by H 2 O 2 was less noticeable may be due to catalase over expression. Therefore, monitoring of ONOO - and reducing oxidative stress should be considered during evaluation of diseases etiology or any kind of drug therapies.","PeriodicalId":13679,"journal":{"name":"Inflammation and cell signaling","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2015-03-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Regulatory role of peroxinitrite (ONOO-) for oxidative damage to human Red Blood Cells (hRBC)\",\"authors\":\"A. Bala, P. Haldar\",\"doi\":\"10.14800/ICS.695\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Monitoring of oxidative stress to human red blood cells (hRBC) is scientifically important for any kind of disease etiology or even during of any drug therapies however the comparative toxicity of reactive species in hRBC in term of hemolysis was not yet established. In this context the present study highlighted the different oxidative assay induced either by superoxide (O 2 - )or by hydrogen peroxide (H 2 O 2 )or by nitric oxide (NO) or by peroxinitrite (ONOO - )using different biochemical reactions in isolated hRBC cells. The oxidative hemolysis was significantly ( p 0.05). The induction of oxidative stress by H 2 O 2 was less noticeable may be due to catalase over expression. Therefore, monitoring of ONOO - and reducing oxidative stress should be considered during evaluation of diseases etiology or any kind of drug therapies.\",\"PeriodicalId\":13679,\"journal\":{\"name\":\"Inflammation and cell signaling\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2015-03-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Inflammation and cell signaling\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.14800/ICS.695\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inflammation and cell signaling","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.14800/ICS.695","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Regulatory role of peroxinitrite (ONOO-) for oxidative damage to human Red Blood Cells (hRBC)
Monitoring of oxidative stress to human red blood cells (hRBC) is scientifically important for any kind of disease etiology or even during of any drug therapies however the comparative toxicity of reactive species in hRBC in term of hemolysis was not yet established. In this context the present study highlighted the different oxidative assay induced either by superoxide (O 2 - )or by hydrogen peroxide (H 2 O 2 )or by nitric oxide (NO) or by peroxinitrite (ONOO - )using different biochemical reactions in isolated hRBC cells. The oxidative hemolysis was significantly ( p 0.05). The induction of oxidative stress by H 2 O 2 was less noticeable may be due to catalase over expression. Therefore, monitoring of ONOO - and reducing oxidative stress should be considered during evaluation of diseases etiology or any kind of drug therapies.