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Volumn 35, Issue 6, 2003, Pages 676-682

Peroxynitrite-mediated oxidation of dichlorodihydrofluorescein and dihydrorhodamine

Author keywords

Dichlorodihydrofluorescein; Dichlorofluorescein; Dichlorofluorescin; Dihydrorhodamine; Fluorescence; Free radicals; Peroxynitrite; Rhodamine

Indexed keywords

CARBON DIOXIDE; CARBONIC ACID DERIVATIVE; DICHLORODIHYDROFLUORESCEIN; DIHYDRORHODAMINE; FLUORESCEIN DERIVATIVE; NITROGEN DIOXIDE; PEROXYNITRITE; REACTIVE OXYGEN METABOLITE; RHODAMINE; UNCLASSIFIED DRUG;

EID: 0042328260     PISSN: 08915849     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0891-5849(03)00389-7     Document Type: Article
Times cited : (61)

References (36)
  • 1
    • 0025874048 scopus 로고
    • Peroxynitrite-induced membrane lipid peroxidation: The cytotoxic potential of superoxide and nitric oxide
    • Radi R., Beckman J.S., Bush K.M., Freeman B.A. Peroxynitrite-induced membrane lipid peroxidation the cytotoxic potential of superoxide and nitric oxide . Arch. Biochem. Biophys. 288:1991;481-487.
    • (1991) Arch. Biochem. Biophys. , vol.288 , pp. 481-487
    • Radi, R.1    Beckman, J.S.2    Bush, K.M.3    Freeman, B.A.4
  • 2
    • 0029805172 scopus 로고    scopus 로고
    • Nitric oxide, superoxide, and peroxynitrite: The good, the bad, and the ugly
    • Beckman J.S., Koppenol W.H. Nitric oxide, superoxide, and peroxynitrite the good, the bad, and the ugly . Am. J. Physiol. Cell Physiol. 271:1996;C1424-C1437.
    • (1996) Am. J. Physiol. Cell Physiol. , vol.271
    • Beckman, J.S.1    Koppenol, W.H.2
  • 5
    • 0030781227 scopus 로고    scopus 로고
    • Formation and properties of peroxynitrite studied by laser flash photolysis, high pressure stopped flow and pulse radiolysis
    • Kissner R., Nauser T., Bugnon P., Lye P.G., Koppenol W.H. Formation and properties of peroxynitrite studied by laser flash photolysis, high pressure stopped flow and pulse radiolysis. Chem. Res. Toxicol. 10:1997;1285-1292.
    • (1997) Chem. Res. Toxicol. , vol.10 , pp. 1285-1292
    • Kissner, R.1    Nauser, T.2    Bugnon, P.3    Lye, P.G.4    Koppenol, W.H.5
  • 6
    • 0037172177 scopus 로고    scopus 로고
    • The rate constant of the reaction of superoxide with nitrogen monoxide: Approaching the diffusion limit
    • Nauser T., Koppenol W.H. The rate constant of the reaction of superoxide with nitrogen monoxide approaching the diffusion limit . J. Phys. Chem. A. 106:2002;4084-4086.
    • (2002) J. Phys. Chem. A , vol.106 , pp. 4084-4086
    • Nauser, T.1    Koppenol, W.H.2
  • 8
    • 0029682870 scopus 로고    scopus 로고
    • Oxidative damage and tyrosine nitration from peroxynitrite
    • Beckman J.S. Oxidative damage and tyrosine nitration from peroxynitrite. Chem. Res. Toxicol. 9:1996;836-844.
    • (1996) Chem. Res. Toxicol. , vol.9 , pp. 836-844
    • Beckman, J.S.1
  • 9
    • 0035954378 scopus 로고    scopus 로고
    • Nitration and oxidation of a hydrophobic tyrosine probe by peroxynitrite in membranes: Comparison with nitration and oxidation of tyrosine by peroxynitrite in aqueous solution
    • Zhang H., Joseph J., Feix J., Hogg N., Kalyanaraman B. Nitration and oxidation of a hydrophobic tyrosine probe by peroxynitrite in membranes comparison with nitration and oxidation of tyrosine by peroxynitrite in aqueous solution . Biochemistry. 40:2001;7675-7686.
    • (2001) Biochemistry , vol.40 , pp. 7675-7686
    • Zhang, H.1    Joseph, J.2    Feix, J.3    Hogg, N.4    Kalyanaraman, B.5
  • 10
    • 0031769737 scopus 로고    scopus 로고
    • Peroxynitrite studied by stopped-flow spectroscopy
    • Kissner R., Beckman J.S., Koppenol W.H. Peroxynitrite studied by stopped-flow spectroscopy. Methods Enzymol. 301:1999;342-352.
    • (1999) Methods Enzymol. , vol.301 , pp. 342-352
    • Kissner, R.1    Beckman, J.S.2    Koppenol, W.H.3
  • 11
    • 0027430156 scopus 로고
    • Dihydrorhodamine 123: A fluorescent probe for superoxide generation
    • Henderson L.M., Chappell J.B. Dihydrorhodamine 123 a fluorescent probe for superoxide generation . Eur. J. Biochem. 217:1993;973-980.
    • (1993) Eur. J. Biochem. , vol.217 , pp. 973-980
    • Henderson, L.M.1    Chappell, J.B.2
  • 12
    • 0032783532 scopus 로고    scopus 로고
    • Dihydrofluorescein diacetate is superior for detecting intracellular oxidants: Comparison with 2′, 7′-dichlorodihydrofluorescein diacetate, 5(and 6)-carboxy-2′, 7′-dichlorodihydrofluorescein diacetate, and dihydrorhodamine 123
    • Hempel S.L., Buettner G.R., O'Malley Y.Q., Wessels D.A., Flaherty D.M. Dihydrofluorescein diacetate is superior for detecting intracellular oxidants comparison with 2′, 7′-dichlorodihydrofluorescein diacetate, 5(and 6)-carboxy-2′, 7′-dichlorodihydrofluorescein diacetate, and dihydrorhodamine 123 . Free Radic. Biol. Med. 27:1999;146-159.
    • (1999) Free Radic. Biol. Med. , vol.27 , pp. 146-159
    • Hempel, S.L.1    Buettner, G.R.2    O'Malley, Y.Q.3    Wessels, D.A.4    Flaherty, D.M.5
  • 13
    • 0030732696 scopus 로고    scopus 로고
    • 2,7-Dihydrodichlorofluorescein diacetate as a fluorescent marker for peroxynitrite formation
    • Possel H., Noack H., Augustin W., Keilhoff G., Wolf G. 2,7-Dihydrodichlorofluorescein diacetate as a fluorescent marker for peroxynitrite formation. FEBS Lett. 416:1997;175-178.
    • (1997) FEBS Lett. , vol.416 , pp. 175-178
    • Possel, H.1    Noack, H.2    Augustin, W.3    Keilhoff, G.4    Wolf, G.5
  • 15
    • 0037048724 scopus 로고    scopus 로고
    • Peroxynitrite scavenging activity of sinapic acid (3,5-dimethoxy-4-hydroxycinnamic acid) isolated from
    • Zou Y., Kim A.R., Choi J.S., Chung H.Y. Peroxynitrite scavenging activity of sinapic acid (3,5-dimethoxy-4-hydroxycinnamic acid) isolated from. Brassica juncea. J. Agric. Food Chem. 50:2002;5884-5890.
    • (2002) Brassica juncea. J. Agric. Food Chem. , vol.50 , pp. 5884-5890
    • Zou, Y.1    Kim, A.R.2    Choi, J.S.3    Chung, H.Y.4
  • 16
    • 0021027358 scopus 로고
    • Detection of picomole levels of hydroperoxides using a fluorescent dichlorofluorescein assay
    • Cathcart R., Schwiers E., Ames B.N. Detection of picomole levels of hydroperoxides using a fluorescent dichlorofluorescein assay. Anal. Biochem. 134:1983;111-116.
    • (1983) Anal. Biochem. , vol.134 , pp. 111-116
    • Cathcart, R.1    Schwiers, E.2    Ames, B.N.3
  • 17
    • 0033214972 scopus 로고    scopus 로고
    • Phenoxyl free radical formation during the oxidation of the fluorescent dye 2′,7′-dichlorofluorescein by horseradish peroxidase. Possible consequences for oxidative stress measurements
    • Rota C., Fann Y.C., Mason R.P. Phenoxyl free radical formation during the oxidation of the fluorescent dye 2′,7′-dichlorofluorescein by horseradish peroxidase. Possible consequences for oxidative stress measurements. J. Biol: Chem. 274:1999;28161-28168.
    • (1999) J. Biol: Chem. , vol.274 , pp. 28161-28168
    • Rota, C.1    Fann, Y.C.2    Mason, R.P.3
  • 19
    • 0031423791 scopus 로고    scopus 로고
    • Dichlorodihydrofluorescein and dihydrorhodamine 123 are sensitive indicators of peroxynitrite in vitro: Implications for intracellular measurement of reactive nitrogen and oxygen species
    • Crow J.P. Dichlorodihydrofluorescein and dihydrorhodamine 123 are sensitive indicators of peroxynitrite in vitro implications for intracellular measurement of reactive nitrogen and oxygen species . Nitric Oxide. 1:1997;145-157.
    • (1997) Nitric Oxide , vol.1 , pp. 145-157
    • Crow, J.P.1
  • 20
    • 0033757902 scopus 로고    scopus 로고
    • 2,7-Dichlorofluorescin oxidation and reactive oxygen species: What does it measure?
    • Jakubowski W., Bartosz G. 2,7-Dichlorofluorescin oxidation and reactive oxygen species what does it measure? Cell. Biol. Int. 24:2000;757-760.
    • (2000) Cell. Biol. Int. , vol.24 , pp. 757-760
    • Jakubowski, W.1    Bartosz, G.2
  • 21
    • 0031018671 scopus 로고    scopus 로고
    • The antioxidant Trolox enhances the oxidation of 2′,7′ -dichlorofluorescin to 2′, 7′-dichlorofluorescein
    • Kalinich J.F., Ramakrishnan N., McClain D.E. The antioxidant Trolox enhances the oxidation of 2′,7′-dichlorofluorescin to 2′, 7′-dichlorofluorescein. Free Radic. Res. 26:1997;37-47.
    • (1997) Free Radic. Res. , vol.26 , pp. 37-47
    • Kalinich, J.F.1    Ramakrishnan, N.2    McClain, D.E.3
  • 22
    • 0035800823 scopus 로고    scopus 로고
    • Reaction of superoxide and nitric oxide with peroxynitrite - Implications for peroxynitrite-mediated oxidation reactions
    • Jourd'heuil D., Jourd'heuil F.L., Kutchukian P.S., Musah R.A., Wink D.A., Grisham M.B. Reaction of superoxide and nitric oxide with peroxynitrite - implications for peroxynitrite-mediated oxidation reactions. in vivo. J. Biol. Chem. 276:2001;28799-28805.
    • (2001) In vivo. J. Biol. Chem. , vol.276 , pp. 28799-28805
    • Jourd'heuil, D.1    Jourd'heuil, F.L.2    Kutchukian, P.S.3    Musah, R.A.4    Wink, D.A.5    Grisham, M.B.6
  • 23
    • 0030721736 scopus 로고    scopus 로고
    • Oxidation of 2′,7′-dichlorofluorescin by peroxynitrite
    • Kooy N.W., Royall J.A., Ischiropoulos H. Oxidation of 2′,7′-dichlorofluorescin by peroxynitrite. Free Radic. Res. 27:1997;245-254.
    • (1997) Free Radic. Res. , vol.27 , pp. 245-254
    • Kooy, N.W.1    Royall, J.A.2    Ischiropoulos, H.3
  • 24
    • 0029834589 scopus 로고    scopus 로고
    • Syntheses of peroxynitrite: To go with the flow or on solid grounds
    • Koppenol W.H., Kissner R., Beckman J.S. Syntheses of peroxynitrite to go with the flow or on solid grounds . Methods Enzymol. 269:1996;296-302.
    • (1996) Methods Enzymol. , vol.269 , pp. 296-302
    • Koppenol, W.H.1    Kissner, R.2    Beckman, J.S.3
  • 26
    • 0037116514 scopus 로고    scopus 로고
    • Product distribution of peroxynitrite decay as a function of pH, temperature, and concentration
    • Kissner R., Koppenol W.H. Product distribution of peroxynitrite decay as a function of pH, temperature, and concentration. J. Am. Chem. Soc. 124:2002;234-239.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 234-239
    • Kissner, R.1    Koppenol, W.H.2
  • 29
    • 0028858786 scopus 로고
    • L. H. NO, nitrosonium ions, nitroxide ions, nitrosothiols and iron-nitrosyls in biology: A chemist's perspective
    • Butler A.R., Flitney F.W., Williams D. L. H. NO, nitrosonium ions, nitroxide ions, nitrosothiols and iron-nitrosyls in biology a chemist's perspective . Trends Pharmacol. Sci. 16:1995;18-22.
    • (1995) Trends Pharmacol. Sci. , vol.16 , pp. 18-22
    • Butler, A.R.1    Flitney, F.W.2    Williams, D.3
  • 30
    • 0027253654 scopus 로고
    • Autoxidation kinetics of aqueous nitric oxide
    • Ford P.C., Wink D.A., Stanbury D.M. Autoxidation kinetics of aqueous nitric oxide. FEBS Lett. 326:1993;1-3.
    • (1993) FEBS Lett. , vol.326 , pp. 1-3
    • Ford, P.C.1    Wink, D.A.2    Stanbury, D.M.3
  • 32
    • 0029799950 scopus 로고    scopus 로고
    • Determination of nitric oxide using fluorescence spectroscopy
    • Miles A.M., Wink D.A., Cook J.C., Grisham M.B. Determination of nitric oxide using fluorescence spectroscopy. Methods Enzymol. 268:1996;105-120.
    • (1996) Methods Enzymol. , vol.268 , pp. 105-120
    • Miles, A.M.1    Wink, D.A.2    Cook, J.C.3    Grisham, M.B.4
  • 33
    • 11944262823 scopus 로고
    • Rapid reaction between peroxonitrite ion and carbon dioxide: Implications for biological activity
    • Lymar S.V., Hurst J.K. Rapid reaction between peroxonitrite ion and carbon dioxide Implications for biological activity . J. Am. Chem. Soc. 117:1995;8867-8868.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 8867-8868
    • Lymar, S.V.1    Hurst, J.K.2
  • 34
    • 0030052854 scopus 로고    scopus 로고
    • Hydroxylation and nitration of phenolic compounds by peroxynitrite
    • Ramezanian M.S., Padmaja S., Koppenol W.H. Hydroxylation and nitration of phenolic compounds by peroxynitrite. Chem. Res, Toxicol. 9:1996;232-240.
    • (1996) Chem. Res, Toxicol. , vol.9 , pp. 232-240
    • Ramezanian, M.S.1    Padmaja, S.2    Koppenol, W.H.3
  • 35
    • 0033783222 scopus 로고    scopus 로고
    • Reactions of peroxynitrite with phenolic and carbonyl compounds
    • Tibi S., Koppenol W.H. Reactions of peroxynitrite with phenolic and carbonyl compounds. Helv. Chim. Acta. 83:2000;2412-2424.
    • (2000) Helv. Chim. Acta , vol.83 , pp. 2412-2424
    • Tibi, S.1    Koppenol, W.H.2


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