Activation of soluble guanylate cyclase by NO donors - S-nitrosothiols, and dinitrosyl-iron complexes with thiol-containing ligands

Nitric Oxide - Biology and Chemistry

Volumn 8, Issue 3, 2003, Pages 155-163

  Severina, Irina S ^a   Bussygina, Olga G ^a   Pyatakova, Natalya V ^a   Malenkova, Irina V ^b   Vanin, Anatoly F ^b  

^a INSTITUTE OF BIOMEDICAL CHEMISTRY   (Russian Federation)

^b SEMENOV INSTITUTE OF CHEMICAL PHYSICS   (Russian Federation)

Author keywords

Dinitrosyl iron complexes; Iron; Nitric oxide; S nitrosothiols; Soluble guanylate cyclase

Indexed keywords

ACETYLCYSTEINE; ACETYLCYSTEINE DERIVATIVE; ASCORBIC ACID; COPPER ION; GLUTATHIONE; GUANYLATE CYCLASE; IRON CHELATE; IRON COMPLEX; LIGAND; METAL ION; NITRIC OXIDE DONOR; PHENANTHROLINE DERIVATIVE; S NITROSOACETYLCYSTEINE; S NITROSOGLUTATHIONE; S NITROSOTHIOL; THIOL DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; COMPLEX FORMATION; CONCENTRATION (PARAMETERS); CONTROLLED STUDY; CYTOSOL; ENZYME ACTIVATION; HUMAN; HUMAN CELL; IRON CHELATION; PRIORITY JOURNAL; TEMPERATURE; THROMBOCYTE;

EID: 0038460763     PISSN: 10898603     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1089-8603(03)00002-8     Document Type: Article

References (36)

1. Katsuki S., Arnold W., Millay C., Murad F. Stimulation of guanylate cyclase by sodium nitroprusside, nitroglycerine and nitric oxide in various tissue preparations and comparision to the effects of sodium azide and hydroxylamine. J. Cyclic Nucleotide Res. 3:1977;23-25.
2. Brandish P.E., Buechler W., Marletta M.A. Regeneration of the ferrous heme of soluble guanylate cyclase from nitric oxide complex: acceleration by thiols and oxyhemoglobin. Biochemistry. 37:1998;16898-16902.
3. Denninger J.W., Marletta M.A. Guanylate cyclase and NO/cGM signalling pathway. Biochim. Biophys. Acta. 1411:1999;334-350.
4. Dierks E.A., Bystrun J.N. The desactivation of soluble guanylate cyclase by redox-active agents. Arch. Biochem. Biophys. 351:1998;1-7.
5. Iesaki T., Gupte S.A., Wolin M.S. A flavoproteine mechanism appears to prevent an oxygen-dependent inhibition of cGMP-associated nitric oxide-elicited relaxation of bovine coronary artery. Circ. Res. 85:1999;1027-1031.
6. Mülsch A., Mordvintcev P., Vanin A.F., Busse R. The potent vasodilating and guanylyl cyclase activating dinitrosyl-iron(II) complex is stored in a potent-bound form in vascular tissue and release by thiols. Biochem. Biophys. Res. Commun. 294:1991;252-256.
7. McDonald C.C., Phillips H.F., Mower H.F. An electron spin resonance study of some complexes with iron, nitric oxide and anionic ligands. J. Am. Chem. Soc. 87:1965;3319-3325.
8. Burbaev D.Sh., Vanin A.F., Blumenfel'd L.A. Electronic and spatial structures of dinitrosyl iron complexes with yarious anionic ligands. Z. Strukt. Khim. (Russian). 12:1971;251-258.
9. Vanin A.F. Dinitrosyl-iron complexes and S-nitrosothiols are two possible forms for stabilization and transport of nitric oxide in biological systems. Biochemistry (Moscow). 67:1998;782-793.
10. Vanin A.F., Malenkova I.V., Serezhenkov V.A. Iron catalyses both decomposition and synthesis of S-nitrosothiols: optical and electron paramagnetic resonance studies. Nitric Oxide. 1:1997;191-203.
11. 2 reaction Chem. Res. Toxicol. 7:1994;5125-5129.
12. Kleschyov A.L., Mordvintcev P.I., Vanin A.F. Role of nitric oxide and iron in hypotensive action of nitrosyl iron complexes with various anion ligands. Stud. Biophys. 105:1985;93-102.
13. Vedernikov Yu.P., Mordvintcev P.I., Malenkova I.V., Vanin A.F. Similarity between the vasorelaxing activity of dinitrosyl-iron complexes and endothelium-derived relaxing factor. Eur. J. Pharmacol. 211:1992;313-317.
14. Mordvintcev P.I., Rudneva V.G., Vanin A.F., Shimkevich L.L., Khodorov B.I. Inhibiting effect of dinitrosyl-iron complexes with low molecular weight ligands on platelet aggregation. Biokhim. (Russia). 51:1986;1851-1857.
15. McAninly J., Williams D.L.H., Askew S.C., Butler A.R., Russel C. Metal ions catalysis in nitrosothiol (RS-NO) decomposition. J. Chem. Soc. Commun. 1993;1758-1759.
16. Williams D.L.H. The mechanism of nitric oxide formation from S-nitrosothiols (thionitrite). Chem. Commun. 1996;1085-1091.
17. Singh R.J., Hogg N., Joseph J., Kalyanaraman B. Mechanism of nitric oxide release from S-nitrosothiols. J. Biol. Chem. 271:1996;18596-18609.
18. + as the effective reagent in nitric oxide formation from S-nitrosothiols (RSNO) J Chem. Soc. Perkin Trans. 2:1996;481-488.
19. Williams D.L.H. The chemistry of S-nitrosothiols. Acc. Chem. Rev. 32:1999;869-876.
20. Vanin A.F., Muller B., Alencar J.L., Lobysheva I.I., Nepveu F., Stoclet J.-C. Evidence that intrinsic iron but not intrinsic copper determines S-nitrosocysteine decomposition in buffer solution. Nitric Oxide. 7:2002;194-209.
21. Chirkov Yu.Yu., Tyshchuk I.A., Belushkina N.N., Severina I.S. Human platelet guanylate cyclase. Biokhim. (Russia) (Engl. Transl.). 52:1987;811-826.
22. Garbers D.L., Murad F. Guanylate cyclase assay method. Adv. Cyclic Nucleotide Res. 10:1979;57-67.
23. Bradford A.M. A rapid sensitive method for quantitation of microgram quantities of protein utilizing the principle of protein-day binding. Anal. Biochem. 72:1976;248-254.
24. Vanin A.F., Stukan R.A., Manukhina E.B. Physical properties of dinitrosyl-iron complexes with thiol-containing ligands in relation with their vasodilatory activity. Biochim. Biophys. Acta. 1295:1996;5-12.
25. Constanza S., Menage S., Purello R., Bonomo R.P., Fontecave M. Re-examination of the formation of dinitrosyl-iron complexes during reaction of S-nitrosothiols with Fe(II). Inorg. Chim. Acta. 318:2001;1-7.
26. LoBello M., Nuceetelli M., Caccuri A.M., Stella L., Paker M.W., Rossojohn J., McKinstry W.J., Mozzi A.F., Federici G., Polizio F., Pederson J.Z., Ricci G. Humam glutathione transferase P1-1 and nitric oxide carriers. J. Biol. Chem. 276:2001;43138-43145.
27. Ueno T., Suzuki Y., Fujii S., Vanin A.F., Yoshimura T. In vivo distribution and behavior of paramagnetic dinitrosyl dithiolato iron complex in the abdomen of mouse. Free Radicals Res. 31:1999;525-534.
28. Jeffrey S.R., Erdjument-Bromage H., Ferris C.D., Tempst P., Snyder S.H. Protein S-nitrosylation: a physiological signal for neuronal nitric oxide. Nat. Cell Biol. 3:2001;193-197.
29. Artz J.D., Toader V., Zavorin S.I., Bennet B.M., Thatcher G.R.T. In vitro activation of soluble guanylyl cyclase and nitric oxide release: a comparision of NO donors and NO mimetics. Biochemistry. 40:2001;9258-9264.
30. Artz J.D., Schmidt B., McCracken J.L., Marletta M.A. Effect of nitroglycerin on soluble guanylate cyclase. J. Biol. Chem. 277:2002;18253-18256.
31. Sheu F.-W., Zhu W., Fung P.C.W. Direct observation of trapping and release of nitric oxide by glutathione and cysteine with electron paramagnetic resonance spectroscopy. Biophys. J. 78:2000;1216-1226.
32. Kurbanov I.S., Mordvintcev P.I., Aliev D.I., Vanin A.F. Influence of thiol compounds and iron on nitric oxide generation from nitroprusside and nitroglycerin. Vopr. Med. Khim. (Russia). 1989;87-90.
33. Beloso P.H., Williams D.L.H. Reversibilty of S-nitrosothiol formation. Chem. Commun. 1997;89-91.
34. Boldyrev A.A., Bulygina E.R., Kramarenko G.G., Vanin A.F. Effect of nitrospcompounds on Na/K-ATPase. Biochim. Biophys. Acta. 1321:1997;243-251.
35. Kim Y.M., Chung H.T., Simmons R.L., Billiar T.R. Cellular non-heme iron content is a determinant of nitric oxide-mediated apoptosis, necrosis and caspase inhibition. J. Biol. Chem. 275:2000;10954-10961.
36. Bush P.M., Whitehead J.P., Pink C.C., Gramm E.C., Eglin J.L., Watton S.P., Pence L.E. Electronic and structural variation among copper (II) complexes with substituted phenanthrolines. Inorg. Chem. 40:2001;1871-1877.