Nitrite is produced by elicited but not by circulating neutrophils
The generation of nitrite (NO2−) was used as an index of the production of nitric oxide by human and rat polymorphonuclear leukocytes (PMN) and rat peritoneal macrophages. Human peripheral blood PMN did not produce significant levels of NO2−. Attempts to induce NO2− generation in human PMN by incuba...
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1993-01-01
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Series: | Mediators of Inflammation |
Online Access: | http://dx.doi.org/10.1155/S0962935193000481 |
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doaj-de60479d674648e1a96ff234facacb0e2020-11-24T23:25:47ZengHindawi LimitedMediators of Inflammation0962-93511466-18611993-01-012534935610.1155/S0962935193000481Nitrite is produced by elicited but not by circulating neutrophilsA. G. Stewart0G. J. Dusting1R. G. Giarracca2T. Harris3Y. Lim4C. G. Sobey5Microsurgery Research Centre, St Vincent's Hospital, Fitzroy, 3065, Victoria, AustraliaDepartment of Physiology, University of Melbourne, Victoria, AustraliaDepartment of Physiology, University of Melbourne, Victoria, AustraliaMicrosurgery Research Centre, St Vincent's Hospital, Fitzroy, 3065, Victoria, AustraliaDepartment of Physiology, University of Melbourne, Victoria, AustraliaDepartment of Pharmacology, University of Melbourne, Victoria, AustraliaThe generation of nitrite (NO2−) was used as an index of the production of nitric oxide by human and rat polymorphonuclear leukocytes (PMN) and rat peritoneal macrophages. Human peripheral blood PMN did not produce significant levels of NO2−. Attempts to induce NO2− generation in human PMN by incubation with GM–CSF (1 nM), TNFα (0.3 nM), endotoxin (1 μg/ml) or formyl-Met-Leu-Phe (100 nM) for up to 16 h were not successful. Addition of human PMN primed by GM–CSF (1 nM) to rabbit aortic ring preparations precontracted with phenylephrine had no effect on tone. In contrast to these observations, PMN, isolated from the peritoneum of oyster glycogen treated rats, generated NO2− via a pathway sensitive to inhibition by the nitric oxide synthase inhibitor, NG-monomethyl L-arginine. However, peripheral blood rat PMN obtained from the same animals did not produce NO2−, even during prolonged incubation for periods of up to 16 h. It is suggested that detectable NO production by PMN requires NO synthase activity to be induced either by the process of PMN migration or by exposure to certain cytokines produced locally at the site of inflammation.http://dx.doi.org/10.1155/S0962935193000481 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
A. G. Stewart G. J. Dusting R. G. Giarracca T. Harris Y. Lim C. G. Sobey |
spellingShingle |
A. G. Stewart G. J. Dusting R. G. Giarracca T. Harris Y. Lim C. G. Sobey Nitrite is produced by elicited but not by circulating neutrophils Mediators of Inflammation |
author_facet |
A. G. Stewart G. J. Dusting R. G. Giarracca T. Harris Y. Lim C. G. Sobey |
author_sort |
A. G. Stewart |
title |
Nitrite is produced by elicited but not by circulating neutrophils |
title_short |
Nitrite is produced by elicited but not by circulating neutrophils |
title_full |
Nitrite is produced by elicited but not by circulating neutrophils |
title_fullStr |
Nitrite is produced by elicited but not by circulating neutrophils |
title_full_unstemmed |
Nitrite is produced by elicited but not by circulating neutrophils |
title_sort |
nitrite is produced by elicited but not by circulating neutrophils |
publisher |
Hindawi Limited |
series |
Mediators of Inflammation |
issn |
0962-9351 1466-1861 |
publishDate |
1993-01-01 |
description |
The generation of nitrite (NO2−) was used as an index of the production of nitric oxide by human and rat polymorphonuclear leukocytes (PMN) and rat peritoneal macrophages. Human peripheral blood PMN did not produce significant levels of NO2−. Attempts to induce NO2− generation in human PMN by incubation with GM–CSF (1 nM), TNFα (0.3 nM), endotoxin (1 μg/ml) or formyl-Met-Leu-Phe (100 nM) for up to 16 h were not successful. Addition of human PMN primed by GM–CSF (1 nM) to rabbit aortic ring preparations precontracted with phenylephrine had no effect on tone. In contrast to these observations, PMN, isolated from the peritoneum of oyster glycogen treated rats, generated NO2− via a pathway sensitive to inhibition by the nitric oxide synthase inhibitor, NG-monomethyl L-arginine. However, peripheral blood rat PMN obtained from the same animals did not produce NO2−, even during prolonged incubation for periods of up to 16 h. It is suggested that detectable NO production by PMN requires NO synthase activity to be induced either by the process of PMN migration or by exposure to certain cytokines produced locally at the site of inflammation. |
url |
http://dx.doi.org/10.1155/S0962935193000481 |
work_keys_str_mv |
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