Concomitant S‐, N‐, and heme‐nitros(yl)ation in biological tissues and fluids: implications for the fate of NO in vivo
Top Cited Papers
Open Access
- 1 November 2002
- journal article
- research article
- Published by Wiley in The FASEB Journal
- Vol. 16 (13) , 1775-1785
- https://doi.org/10.1096/fj.02-0363com
Abstract
There is growing evidence for the involvement of nitric oxide (NO) ‐mediated nitrosation in cell signaling and pathology. Although S‐nitrosothiols (RSNOs) have been frequently implicated in these processes, it is unclear whether NO forms nitrosyl adducts with moieties other than thiols. A major obstacle in assessing the significance of formation of nitro‐sated species is the limited reliability of available analytical techniques for measurements in complex biological matrices. Here we report on the presence of nitrosated compounds in plasma and erythrocytes of rats, mice, guinea pigs, and monkeys under basal conditions, in immunologically challenged murine macrophages in vitro and laboratory animals in vivo. Besides RSNOs, all biological samples also contained mercury‐stable nitroso species, indicating the additional involvement of amine and heme nitros(yl)ation reactions. Significant differences in the amounts and ratios of RSNOs over N‐and heme‐nitros(yl)ated compounds were found between species and organs. These observations were made possible by the development of a novel gas‐phase chemiluminescence‐based technique that allows detection of nitroso species in tissues and biological fluids without prior extraction or deproteinization. The method can quantify as little as 100 fmol bound NO and has been validated extensively for use in different biological matrices. Discrimination between nitrite, RSNOs, and N‐nitroso or nitrosylheme compounds is accomplished by use of group‐specific reagents. Our findings suggest that NO generation in vivo leads to concomitant formation of RSNOs, nitrosamines, and nitrosylhemes with considerable variation between rodents and primates, highlighting the difficulty in comparing data between different animal models and extrapolating results from experimental animals to human physiology.—Feelisch, M., Rassaf, T., Mnaimneh, S., Singh, N., Bryan, N. S., Jourd'heuil, D., Kelm, M. Concomitant S‐, N‐, and heme‐nitros(yl)ation in biological tissues and fluids: implications for the fate of NO in vivo. FASEB J. 16, 1775–1785 (2002)Keywords
Funding Information
- Deutsche Forschungsgemeinschaft
- National Institutes of Health (HL69029-01, CA89366)
This publication has 36 references indexed in Scilit:
- Biochemical Characterization ofS-NitrosohemoglobinJournal of Biological Chemistry, 1999
- Reductive Assays forS-Nitrosothiols: Implications for Measurements in Biological SystemsBiochemical and Biophysical Research Communications, 1998
- A Novel Reaction Mechanism for the Formation of S-Nitrosothiol in VivoJournal of Biological Chemistry, 1997
- Nitrosation of Tryptophan Residue(s) in Serum Albumin and Model DipeptidesPublished by Elsevier ,1996
- S-nitrosohaemoglobin: a dynamic activity of blood involved in vascular controlNature, 1996
- S-Nitrosation of Serum Albumin by Dinitrosyl-Iron ComplexJournal of Biological Chemistry, 1995
- Relative Standard Electrode Potentials of I3−/I−, I2/I3−, and I2/I− Redox Couples and the Related Formation Constants of I3− in Some Pure and Mixed Dipolar Aprotic SolventsBulletin of the Chemical Society of Japan, 1988
- Determination of a non-volatile N-nitrosamine on a food matrixThe Analyst, 1978
- Kinetics of Fischer-Hepp rearrangementThe Journal of Organic Chemistry, 1970
- Mechanism of chemiluminescent reaction between nitric oxide and ozoneTransactions of the Faraday Society, 1967