Suppression of NO production and 8-nitroguanosine formation by phenol-containing endocrine-disrupting chemicals in LPS-stimulated macrophages: Involvement of estrogen receptor-dependent or -independent pathways

Nitric Oxide - Biology and Chemistry

Volumn 18, Issue 3, 2008, Pages 223-228

  Yoshitake, Jun ^a   Kato, Katsuaki ^b   Yoshioka, Daisuke ^a,c   Sueishi, Yoshimi ^c   Sawa, Tomohiro ^d   Akaike, Takaaki ^d   Yoshimura, Tetsuhiko ^a  

^a Yamagata Promotional Organization for Industrial Technology   (Japan)

^b MIYAGI CANCER CENTER   (Japan)

^c OKAYAMA UNIVERSITY   (Japan)

^d KUMAMOTO UNIVERSITY   (Japan)

Author keywords

8 Nitroguanosine; Endocrine disrupting chemicals; Estrogen receptor; iNOS; NF B; Nitric oxide

Indexed keywords

2,4 DICHLOROPHENOL; 4 NONYLPHENOL; 4 OCTYLPHENOL; 4,4' ISOPROPYLIDENEDIPHENOL; 8 NITROGUANOSINE; ENDOCRINE DISRUPTOR; ESTROGEN RECEPTOR; FULVESTRANT; GUANOSINE DERIVATIVE; IMMUNOGLOBULIN ENHANCER BINDING PROTEIN; LIPOPOLYSACCHARIDE; NITRIC OXIDE; PENTACHLOROPHENOL; TRANSCRIPTION FACTOR RELA; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; CELL STIMULATION; CONTROLLED STUDY; DNA BINDING; ENZYME LINKED IMMUNOSORBENT ASSAY; IMMUNOCYTOCHEMISTRY; MACROPHAGE; MOUSE; NONHUMAN; PRIORITY JOURNAL;

ANIMALS; CELLS, CULTURED; DOSE-RESPONSE RELATIONSHIP, DRUG; ENDOCRINE DISRUPTORS; ESTRADIOL; GUANOSINE; LIPOPOLYSACCHARIDES; MACROPHAGES; MICE; NF-KAPPA B; NITRIC OXIDE; NITRO COMPOUNDS; PHENOLS; RECEPTORS, ESTROGEN; SIGNAL TRANSDUCTION;

EID: 41149107750     PISSN: 10898603     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.niox.2008.01.003     Document Type: Article

References (27)

1. Terasaka S., Inoue A., Tanji M., and Kiyama R. Expression profiling of estrogen-responsive gene in breast cancer cell treated with alkylphenols, chlorinated phenols, parabens, or bis- and benzoylphenols for evaluation of estrogenic activity. Toxicol. Lett. 163 (2006) 130-141
2. Shelby M.D., Newbold R.R., Tully D.B., Chae K., and Davis V.L. Assessing environmental chemicals for estrogenicity using a combination of in vitro and in vivo assays. Environ. Health Perspect. 104 (1996) 1296-1300
3. Kuiper G.G., Lemmen J.G., Carlsson B., Corton J.C., Safe S.H., van der Saag P.T., van der Burg B., and Gustafsson J.A. Interaction of estrogenic chemicals and phytoestrogens with estrogen receptor β. Endocrinology 139 (1998) 4245-4263
4. Savita, and Rai U. Sex steroid hormones modulate the activation of murine peritoneal macrophages: receptor mediated modulation. Comp. Biochem. Physiol. 119C (1998) 199-204
5. You H.J., Kim J.Y., and Jeong H.G. 17β-Estradiol increases inducible nitric oxide synthase expression in macrophages. Biochem. Biophys. Res. Commun. 303 (2003) 1129-1134
6. Karpuzoglu E., Fenaux J.B., Phillips R.A., Lengi A.J., Elvinger F., and Ahmed S.A. Estrogen up-regulates inducible nitric oxide synthase, nitric oxide, and cyclooxygenase-2 in splenocytes activated with T cell stimulants: role of interferon-γ. Endocrinology 147 (2006) 662-671
7. Chen Z., Yuhanna I.S., Galcheva-Gargona Z., Karas R.H., Mendelsohn M.E., and Shaul P.W. Estrogen receptor α mediates the nongenomic activation of endothelial nitric oxide synthase by estrogen. J. Clin. Invest. 103 (1999) 401-406
8. Akira S., Uematsu S., and Takeuchi O. Pathogen recognition and innate immunity. Cell 124 (2006) 783-801
9. Kleinert H., Pautz A., Linker K., and Schwarz P.M. Regulation of the expression of inducible nitric oxide synthase. Eur. J. Pharmacol. 500 (2004) 255-266
10. Akaike T., Okamoto S., Sawa T., Yoshitake J., Tamura F., Ichimori K., Miyazaki K., Sasamoto K., and Maeda H. 8-Nitroguanosine formation in viral pneumonia and its implication for pathogenesis. Proc. Natl. Acad. Sci. USA 100 (2003) 685-690
11. Smiley S.T., Reers M., Mottola-Hartshorn C., Lin M., Chen A., Smith T.W., Steele Jr. G.D., and Chen L.B. Intracellular heterogeneity in mitochondrial membrane potentials revealed by a J-aggregate-forming lipophilic cation JC-1. Proc. Natl. Acad. Sci. USA 88 (1991) 3671-3675
12. Terasaki Y., Akuta T., Terasaki M., Sawa T., Mori T., Okamoto T., Ozaki M., Takeya M., and Akaike T. Guanine nitration in idiopathic pulmonary fibrosis and its implication for carcinogenesis. Am. J. Respir. Crit. Care Med. 174 (2006) 665-673
13. Zamboni L., Mishell Jr. D.R., Bell J.H., and Baca M. Fine structure of the human ovum in the pronuclear stage. J. Cell Biol. 30 (1966) 579-600
14. Bosscher K.D., Berghe W.V., and Haegeman G. Cross-talk between nuclear receptors and nuclear factor κB. Oncogene 25 (2006) 6868-6886
15. Kim J.Y., and Jeong H.G. Down-regulation of inducible nitric oxide synthase and tumor necrosis factor-α expression by bisphenol A via nuclear factor-κB inactivation in macrophages. Cancer Lett. 196 (2003) 69-76
16. You H.J., Choi C.Y., Jeon Y.J., Chung Y.C., Kang S.K., Hahm K.S., and Jeong H.G. Suppression of inducible nitric oxide synthase and tumor necrosis factor-α expression by 4-nonylphenol in macrophages. Biochem. Biophys. Res. Commun. 294 (2002) 753-759
17. Weinbach E.C., and Garbus J. The interaction of uncoupling phenols with mitochondria and with mitochondrial protein. J. Biol. Chem. 240 (1965) 1811-1819
18. Fleischer M., Meiss R., Robenek H., Themann H., and Eckard R. Ultrastructural morphometric investigations on rat liver of young and adult rats after treatment with technical pentachlorophenol (PCP). Arch. Toxicol. 44 (1980) 243-257
19. Schreck R., Rieber P., and Baeuerle P.A. Reactive oxygen intermediates as apparently widely used messengers in the activation of the NF-κB transcription factor and HIV-1. EMBO J. 10 (1991) 2247-2258
20. Kotake Y., Sang H., Miyajima T., and Wallis G.L. Inhibition of NF-κB, iNOS mRNA, COX2 mRNA, and COX catalytic activity by phenyl-N-tert-butylnitrone (PBN). Biochim. Biophys. Acta 1448 (1998) 77-84
21. Luo Y., Wang X.R., Shi H.H., Mao D.Q., Sui Y.X., and Ji L.L. Electron paramagnetic resonance investigation of in vivo free radical formation and oxidative stress induced by 2,4-dichlorophenol in the freshwater fish Carassius auratus. Environ. Toxicol. Chem. 24 (2005) 2145-2153
22. Beckman J.S., and Koppenol W.H. Nitric oxide, superoxide, and peroxynitrite: the good, the bad, and ugly. Am. J. Physiol. 271 (1996) C1424-C1437
23. Stamler J.S., Single D.J., and Loscalzo J. Biochemistry of nitric oxide and its redox-activated forms. Science 258 (1992) 1898-1902
24. Estevez A.G., Crow J.P., Sampson J.B., Reiter C., Zhuang Y., Richardson G.J., Tarpey M.M., Barbeito L., and Beckman J.S. Induction of nitric oxide-dependent apoptosis in motor neurons by zinc-deficient superoxide dismutase. Science 286 (1999) 2498-2500
25. Yoshitake J., Akaike T., Akuta T., Tamura F., Ogura T., Esumi H., and Maeda H. Nitric oxide as an endogenous mutagen for Sendai virus without antiviral effect. J. Virol. 78 (2004) 8709-8719
26. Ma N., Adachi Y., Hiraku Y., Horiki N., Horiike S., Imoto I., Pinlaor S., Murata M., Semba R., and Kawanishi S. Accumulation of 8-nitroguanosine in human gastric epithelium induced by Helicobacter pylori infection. Biochem. Biophys. Res. Commun. 319 (2004) 506-510
27. Akuta T., Zaki M.H., Yoshitake J., Okamoto T., and Akaike T. Nitrative stress through formation of 8-nitroguanosine: insights into microbial pathogenesis. Nitric Oxide 14 (2006) 101-108