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Volumn 516, Issue 3, 2005, Pages 260-267

Nω-hydroxy-L-arginine homologues and hydroxylamine as nitric oxide-dependent vasorelaxant agents

Author keywords

Electron paramagnetic resonance; Hydroxylamine; N hydroxy L arginine homologue; Nitric oxide release; Vasorelaxation

Indexed keywords

12 (N OMEGA HYDROXYARGININE); 1H 1,2,4 OXADIAZOLO[4,3 A]QUINOXALIN 1 ONE; 2 PHENYL 4,4,5,5 TETRAMETHYLIMIDAZOLINE 1 OXYL 3 OXIDE; 4 (DINOR N OMEGA HYDROXYARGININE); 8 (NOR N OMEGA HYDROXYARGININE); 8 BROMO CYCLIC GMP; 9 (HOMO N OMEGA HYDROXYARGININE); ALPHA AMINO ACID; ARGININE DERIVATIVE; CYTOCHROME P450 INHIBITOR; ETHOXYRESORUFIN; GUANIDINE DERIVATIVE; GUANYLATE CYCLASE; GUANYLATE CYCLASE INHIBITOR; HYDROXYLAMINE; N(G) NITROARGININE METHYL ESTER; NITRIC OXIDE; NITRIC OXIDE SYNTHASE; SCAVENGER; UNCLASSIFIED DRUG; 1H (1,2,4)OXADIAZOLO(4,3 A)QUINOXALIN 1 ONE; 1H-(1,2,4)OXADIAZOLO(4,3-A)QUINOXALIN-1-ONE; 2-PHENYL-4,4,5,5-TETRAMETHYLIMIDAZOLINE-1-OXYL-3-OXIDE; AMINE OXIDE; ARGININE; CYCLIC GMP; DRUG DERIVATIVE; ENZYME INHIBITOR; IMIDAZOLE DERIVATIVE; N(OMEGA) HYDROXYARGININE; N(OMEGA)-HYDROXYARGININE; OXADIAZOLE DERIVATIVE; QUINOXALINE DERIVATIVE; VASODILATOR AGENT;

EID: 21544438206     PISSN: 00142999     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejphar.2005.04.021     Document Type: Article
Times cited : (16)

References (34)
  • 3
    • 0032797908 scopus 로고    scopus 로고
    • Biochemical and functional profile of a newly developed potent and isozyme-selective arginase inhibitor
    • R. Baggio, F.A. Emig, D.W. Christianson, D.E. Ash, S. Chakder, and S. Rattan Biochemical and functional profile of a newly developed potent and isozyme-selective arginase inhibitor J. Pharmacol. Exp. Ther. 290 1999 1409 1416
    • (1999) J. Pharmacol. Exp. Ther. , vol.290 , pp. 1409-1416
    • Baggio, R.1    Emig, F.A.2    Christianson, D.W.3    Ash, D.E.4    Chakder, S.5    Rattan, S.6
  • 4
    • 0026773733 scopus 로고
    • Formation of nitrogen oxides and citrulline upon oxidation of N-omega-hydroxy-l-arginine by hemeproteins
    • J.L. Boucher, A. Genet, S. Vadon, M. Delaforge, and D. Mansuy Formation of nitrogen oxides and citrulline upon oxidation of N-omega-hydroxy-l-arginine by hemeproteins Biochem. Biophys. Res. Commun. 184 1992 1158 1164
    • (1992) Biochem. Biophys. Res. Commun. , vol.184 , pp. 1158-1164
    • Boucher, J.L.1    Genet, A.2    Vadon, S.3    Delaforge, M.4    Mansuy, D.5
  • 6
    • 0034898074 scopus 로고    scopus 로고
    • Oxidation of the ketoxime acetoxime to nitric oxide by oxygen radical-generating systems
    • A.A. Caro, A.I. Cederbaum, and D.A. Stoyanovsky Oxidation of the ketoxime acetoxime to nitric oxide by oxygen radical-generating systems Nitric Oxide 5 2001 413 424
    • (2001) Nitric Oxide , vol.5 , pp. 413-424
    • Caro, A.A.1    Cederbaum, A.I.2    Stoyanovsky, D.A.3
  • 8
    • 0034731352 scopus 로고    scopus 로고
    • Pharmacological profile of nitrergic nerve-, nitric oxide-, nitrosoglutathione- and hydroxylamine-induced relaxations of the rat duodenum
    • N.A. Correira, R.B. Oliviera, and G. Ballejo Pharmacological profile of nitrergic nerve-, nitric oxide-, nitrosoglutathione- and hydroxylamine-induced relaxations of the rat duodenum Life Sci. 66 2000 709 717
    • (2000) Life Sci. , vol.66 , pp. 709-717
    • Correira, N.A.1    Oliviera, R.B.2    Ballejo, G.3
  • 10
    • 0024435012 scopus 로고
    • Hydroxylamine is a vasorelaxant and a possible intermediate in the oxidative conversion of l-arginine to nitric oxide
    • E.G. DeMaster, L. Raij, S.L. Archer, and E.K. Weir Hydroxylamine is a vasorelaxant and a possible intermediate in the oxidative conversion of l-arginine to nitric oxide Biochem. Biophys. Res. Commun. 163 1989 527 533
    • (1989) Biochem. Biophys. Res. Commun. , vol.163 , pp. 527-533
    • Demaster, E.G.1    Raij, L.2    Archer, S.L.3    Weir, E.K.4
  • 12
    • 0036065962 scopus 로고    scopus 로고
    • Vasoprotection by nitric oxide: Mechanisms and therapeutic potential
    • M.T. Gewaltig, and G. Kojda Vasoprotection by nitric oxide: mechanisms and therapeutic potential Cardiovasc. Res. 55 2002 250 260
    • (2002) Cardiovasc. Res. , vol.55 , pp. 250-260
    • Gewaltig, M.T.1    Kojda, G.2
  • 13
    • 0032524814 scopus 로고    scopus 로고
    • + channel blockers in rat aortic rings
    • + channel blockers in rat aortic rings Eur. J. Pharmacol. 349 1998 53 60
    • (1998) Eur. J. Pharmacol. , vol.349 , pp. 53-60
    • Huang, Y.1
  • 14
    • 0033551927 scopus 로고    scopus 로고
    • Neuronal nitric oxide synthase catalyzes the reduction of 7-ethoxyresorufin
    • H.B. Jiang, and Y. Ichikawa Neuronal nitric oxide synthase catalyzes the reduction of 7-ethoxyresorufin Life Sci. 65 1999 1257 1264
    • (1999) Life Sci. , vol.65 , pp. 1257-1264
    • Jiang, H.B.1    Ichikawa, Y.2
  • 15
    • 0032497909 scopus 로고    scopus 로고
    • 450 dependent oxidation of N-hydroxyguanidines, amidoximes, and ketoximes: Mechanism of the oxidative cleavage of their CN(OH) bond with formation of nitrogen oxides
    • 450 dependent oxidation of N-hydroxyguanidines, amidoximes, and ketoximes: mechanism of the oxidative cleavage of their CN(OH) bond with formation of nitrogen oxides Biochemistry 37 1998 17179 17191
    • (1998) Biochemistry , vol.37 , pp. 17179-17191
    • Jousserandot, A.1    Boucher, J.L.2    Henry, Y.3    Niklaus, B.4    Clement, B.5    Mansuy, D.6
  • 16
    • 0027292075 scopus 로고
    • Multiple catalytic functions of brain nitric oxide synthase. Biochemical characterization, cofactor-requirement, and the role of N-omega-hydroxy-l- arginine as an intermediate
    • P. Klatt, K. Schmidt, G. Uray, and B. Mayer Multiple catalytic functions of brain nitric oxide synthase. Biochemical characterization, cofactor-requirement, and the role of N-omega-hydroxy-l-arginine as an intermediate J. Biol. Chem. 268 1993 14781 14787
    • (1993) J. Biol. Chem. , vol.268 , pp. 14781-14787
    • Klatt, P.1    Schmidt, K.2    Uray, G.3    Mayer, B.4
  • 19
    • 0034843632 scopus 로고    scopus 로고
    • Nitric oxide generation from hydroxylamine in the presence of neutrophils and in the cell free system
    • M. Klink, A. Swierzko, and Z. Sulowska Nitric oxide generation from hydroxylamine in the presence of neutrophils and in the cell free system APMIS 109 2001 493 499
    • (2001) APMIS , vol.109 , pp. 493-499
    • Klink, M.1    Swierzko, A.2    Sulowska, Z.3
  • 20
    • 0032555182 scopus 로고    scopus 로고
    • Substrate specificity of NO synthases: Detailed comparison of l-arginine, homo-l-arginine, their N-omega-hydroxy derivatives, and N-omega-hydroxynor-l- arginine
    • C. Moali, J.L. Boucher, M.A. Sari, D.J. Stuehr, and D. Mansuy Substrate specificity of NO synthases: detailed comparison of l-arginine, homo-l-arginine, their N-omega-hydroxy derivatives, and N-omega-hydroxynor-l-arginine Biochemistry 37 1998 10453 10460
    • (1998) Biochemistry , vol.37 , pp. 10453-10460
    • Moali, C.1    Boucher, J.L.2    Sari, M.A.3    Stuehr, D.J.4    Mansuy, D.5
  • 21
    • 0034682557 scopus 로고    scopus 로고
    • Recognition of α-amino acids bearing various CNOH functions by nitric oxide synthase and arginase involves very different structural determinants
    • C. Moali, M. Brolo, J. Custot, M.A. Sari, J.L. Boucher, D.J. Stuehr, and D. Mansuy Recognition of α-amino acids bearing various CNOH functions by nitric oxide synthase and arginase involves very different structural determinants Biochemistry 39 2000 8208 8218
    • (2000) Biochemistry , vol.39 , pp. 8208-8218
    • Moali, C.1    Brolo, M.2    Custot, J.3    Sari, M.A.4    Boucher, J.L.5    Stuehr, D.J.6    Mansuy, D.7
  • 22
    • 0001105563 scopus 로고
    • The reactions of azide with catalase and their significance
    • P. Nicholls The reactions of azide with catalase and their significance Biochem. J. 90 1964 331 343
    • (1964) Biochem. J. , vol.90 , pp. 331-343
    • Nicholls, P.1
  • 23
    • 0030804868 scopus 로고    scopus 로고
    • Nitric oxide generation from sodium nitroprusside and hydroxylamine in brain
    • K. Ohta, G. Rosner, and R. Graf Nitric oxide generation from sodium nitroprusside and hydroxylamine in brain NeuroReport 8 1997 2229 2235
    • (1997) NeuroReport , vol.8 , pp. 2229-2235
    • Ohta, K.1    Rosner, G.2    Graf, R.3
  • 24
    • 0027320848 scopus 로고
    • ω-hydroxy-l-arginine to citrulline and nitrogen oxides and occurrence in NO synthases of a sequence very similar to the heme binding sequence in P450s
    • ω-hydroxy-l-arginine to citrulline and nitrogen oxides and occurrence in NO synthases of a sequence very similar to the heme binding sequence in P450s Biochem. Biophys. Res. Commun. 192 1993 53 60
    • (1993) Biochem. Biophys. Res. Commun. , vol.192 , pp. 53-60
    • Renaud, J.P.1    Boucher, J.L.2    Vadon, S.3    Delaforge, M.4    Mansuy, D.5
  • 25
    • 0025102785 scopus 로고
    • Basal and stimulated formation and release of l-arginine-derived nitrogen oxides from cultured endothelial cells
    • H.H. Schmidt, B. Zernikow, S. Baeblich, and E. Bohme Basal and stimulated formation and release of l-arginine-derived nitrogen oxides from cultured endothelial cells J. Pharmacol. Exp. Ther. 254 1990 591 597
    • (1990) J. Pharmacol. Exp. Ther. , vol.254 , pp. 591-597
    • Schmidt, H.H.1    Zernikow, B.2    Baeblich, S.3    Bohme, E.4
  • 26
    • 0029156528 scopus 로고
    • Superoxide anion efficiently performs the oxidative cleavage of CNOH bonds of amidoximes and N-hydroxyguanidines with formation of nitrogen oxides
    • N. Sennequier, J.L. Boucher, P. Battioni, and D. Mansuy Superoxide anion efficiently performs the oxidative cleavage of CNOH bonds of amidoximes and N-hydroxyguanidines with formation of nitrogen oxides Tetrahedron Lett. 36 1995 6059 6062
    • (1995) Tetrahedron Lett. , vol.36 , pp. 6059-6062
    • Sennequier, N.1    Boucher, J.L.2    Battioni, P.3    Mansuy, D.4
  • 27
    • 0025892441 scopus 로고
    • N-omega-hydroxy-l-arginine is an intermediate in the biosynthesis of nitric oxide from l-arginine
    • D.J. Stuehr, N.S. Kwon, C.F. Nathan, O.W. Griffith, P.L. Feldman, and J. Wiseman N-omega-hydroxy-l-arginine is an intermediate in the biosynthesis of nitric oxide from l-arginine J. Biol. Chem. 266 1991 6259 6263
    • (1991) J. Biol. Chem. , vol.266 , pp. 6259-6263
    • Stuehr, D.J.1    Kwon, N.S.2    Nathan, C.F.3    Griffith, O.W.4    Feldman, P.L.5    Wiseman, J.6
  • 28
    • 17844382387 scopus 로고    scopus 로고
    • The effect of hydroxylamine on KATP channels in vascular smooth muscle and underlying mechanisms
    • G. Tang, L. Wu, and R. Wang The effect of hydroxylamine on KATP channels in vascular smooth muscle and underlying mechanisms Mol. Pharmacol. 67 2005 1723 1731
    • (2005) Mol. Pharmacol. , vol.67 , pp. 1723-1731
    • Tang, G.1    Wu, L.2    Wang, R.3
  • 30
    • 0024462845 scopus 로고
    • Vascular relaxation mediated by hydroxylamines and oximes: Their conversion to nitrites and mechanism of endothelium dependent vascular relaxation
    • G. Thomas, and P.W. Ramwell Vascular relaxation mediated by hydroxylamines and oximes: their conversion to nitrites and mechanism of endothelium dependent vascular relaxation Biochem. Biophys. Res. Commun. 164 1989 889 893
    • (1989) Biochem. Biophys. Res. Commun. , vol.164 , pp. 889-893
    • Thomas, G.1    Ramwell, P.W.2
  • 32
    • 0023607527 scopus 로고
    • Cyclic GMP synthesis and function
    • S.A. Waldman, and F. Murad Cyclic GMP synthesis and function Pharmacol. Rev. 39 1987 163 196
    • (1987) Pharmacol. Rev. , vol.39 , pp. 163-196
    • Waldman, S.A.1    Murad, F.2
  • 33
    • 0025799631 scopus 로고
    • ω-hydroxy-l-arginine: A novel arginine analog capable of causing vasorelaxation in bovine intrapulmonary artery
    • ω-hydroxy-l- arginine: a novel arginine analog capable of causing vasorelaxation in bovine intrapulmonary artery Biochem. Biophys. Res. Commun. 176 1991 528 534
    • (1991) Biochem. Biophys. Res. Commun. , vol.176 , pp. 528-534
    • Wallace, G.C.1    Gulati, P.2    Fukuto, J.M.3
  • 34
    • 0026457428 scopus 로고
    • Potentiation of the vasorelaxant activity of nitric oxide by hydroxyguanidine: Implications for the nature of endothelium-derived relaxing factor
    • A. Zembowicz, T.A. Swierkosz, G.J. Southan, M. Hecker, and J.R. Vane Potentiation of the vasorelaxant activity of nitric oxide by hydroxyguanidine: implications for the nature of endothelium-derived relaxing factor Br. J. Pharmacol. 107 1992 1001 1007
    • (1992) Br. J. Pharmacol. , vol.107 , pp. 1001-1007
    • Zembowicz, A.1    Swierkosz, T.A.2    Southan, G.J.3    Hecker, M.4    Vane, J.R.5


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