메뉴 건너뛰기




Volumn 43, Issue 2, 2008, Pages 65-68

Role of linoleic acid hydroperoxide preformed by cyclooxygenase-1 or -2 on the regulation of prostaglandin formation from arachidonic acid by the respective enzyme

Author keywords

Arachidonic acid; Cyclooxygenase 1; Cyclooxygenase 2; Linoleic acid hydroperoxide; Prostaglandin

Indexed keywords

ARACHIDONIC ACID; CYCLOOXYGENASE 1; CYCLOOXYGENASE 2; HYDROPEROXIDE; HYDROPEROXY 9,11 OCTADECANOIC ACID; LINOLEIC ACID; PROSTAGLANDIN; PROSTAGLANDIN D2; PROSTAGLANDIN E2; PROSTAGLANDIN F2 ALPHA; STEARIC ACID; UNCLASSIFIED DRUG;

EID: 54949135192     PISSN: 09120009     EISSN: None     Source Type: Journal    
DOI: 10.3164/jcbn.2008047     Document Type: Article
Times cited : (6)

References (23)
  • 1
    • 4143107932 scopus 로고    scopus 로고
    • Cyclooxygenase isozymes: The biology of prostaglandin synthesis and inhibition
    • Simmons, D.L., Botting, R.M., and Hla, T.: Cyclooxygenase isozymes: the biology of prostaglandin synthesis and inhibition. Pharmacol. Rev., 56, 387-437, 2004.
    • (2004) Pharmacol. Rev , vol.56 , pp. 387-437
    • Simmons, D.L.1    Botting, R.M.2    Hla, T.3
  • 2
    • 0032464008 scopus 로고    scopus 로고
    • The advent of highly selective inhibitors of cyclooxygenase - a review
    • Cryer, B. and Dubois, A.: The advent of highly selective inhibitors of cyclooxygenase - a review. Prostaglandins Other Lipid Mediat., 56, 341-361, 1998.
    • (1998) Prostaglandins Other Lipid Mediat , vol.56 , pp. 341-361
    • Cryer, B.1    Dubois, A.2
  • 4
    • 0032701224 scopus 로고    scopus 로고
    • The cyclooxygenase isoforms: Structural insights into the conversion of arachidonic acid to prostaglandins
    • Garavito, R.M. and DeWitt, D.L.: The cyclooxygenase isoforms: structural insights into the conversion of arachidonic acid to prostaglandins. Biochim. Biophys. Acta, 1441, 278-287, 1999.
    • (1999) Biochim. Biophys. Acta , vol.1441 , pp. 278-287
    • Garavito, R.M.1    DeWitt, D.L.2
  • 5
    • 0014302205 scopus 로고
    • Inhibition of prostaglandin synthesis by oleic, linoleic and linolenic acids
    • Pace-Asciak, C. and Wolfe, L.S.: Inhibition of prostaglandin synthesis by oleic, linoleic and linolenic acids. Biochim. Biophys. Acta, 152, 784-787, 1968.
    • (1968) Biochim. Biophys. Acta , vol.152 , pp. 784-787
    • Pace-Asciak, C.1    Wolfe, L.S.2
  • 6
    • 0015845467 scopus 로고
    • 2 in human skin: Subcellular localization and inhibition by unsaturated fatty acids and anti-inflammatory drugs
    • 2 in human skin: subcellular localization and inhibition by unsaturated fatty acids and anti-inflammatory drugs. J. Lipid Res., 14, 377-384, 1973.
    • (1973) J. Lipid Res , vol.14 , pp. 377-384
    • Ziboh, V.A.1
  • 9
    • 0021825288 scopus 로고
    • Release of prostaglandin and monohydroxy and trihydroxy metabolites of linoleic and arachidonic acids by adult and fetal aortae and ductus arteriosus
    • Funk, C.D. and Powell, W.S.: Release of prostaglandin and monohydroxy and trihydroxy metabolites of linoleic and arachidonic acids by adult and fetal aortae and ductus arteriosus. J. Biol. Chem., 260, 7481-7488, 1985.
    • (1985) J. Biol. Chem , vol.260 , pp. 7481-7488
    • Funk, C.D.1    Powell, W.S.2
  • 10
    • 0024402179 scopus 로고
    • Synthesis of hydroxy fatty acids from linoleic acid by human blood platelets
    • Daret, D., Blin, P., and Larrue, J.: Synthesis of hydroxy fatty acids from linoleic acid by human blood platelets. Prostaglandins, 38, 203-214, 1989.
    • (1989) Prostaglandins , vol.38 , pp. 203-214
    • Daret, D.1    Blin, P.2    Larrue, J.3
  • 11
    • 0028176379 scopus 로고
    • Effect of 13-hydroperoxy-9,11-octadecadienoic acid (13-HPODE) on arachidonic acid metabolism in rabbit platelets
    • Fujimoto, Y., Sumiya, T., Tsunomori, M., Nishida, H., Sakuma, S., and Fujita, T.: Effect of 13-hydroperoxy-9,11-octadecadienoic acid (13-HPODE) on arachidonic acid metabolism in rabbit platelets. Int. J. Biochem., 26, 127-131, 1994.
    • (1994) Int. J. Biochem , vol.26 , pp. 127-131
    • Fujimoto, Y.1    Sumiya, T.2    Tsunomori, M.3    Nishida, H.4    Sakuma, S.5    Fujita, T.6
  • 13
    • 0025350080 scopus 로고
    • Effective use of rabbit gastric antral mucosal slices in prostaglandin synthesis and metabolism studies
    • Fujimoto, Y., Nakatani, E., Minamino, H., Takahashi, M., Sakuma, S., and Fujita, T.: Effective use of rabbit gastric antral mucosal slices in prostaglandin synthesis and metabolism studies. Biochim. Biophys. Acta, 1044, 65-69, 1990.
    • (1990) Biochim. Biophys. Acta , vol.1044 , pp. 65-69
    • Fujimoto, Y.1    Nakatani, E.2    Minamino, H.3    Takahashi, M.4    Sakuma, S.5    Fujita, T.6
  • 15
    • 0028089109 scopus 로고
    • NS-398, a new anti-inflammatory agent, selectively inhibits prostaglandin G/H synthase/cyclooxygenase (COX-2) activity in vitro
    • Futaki, N., Takahashi, S., Yokoyama, M., Arai, I., Higuchi, S., and Otomo, S.: NS-398, a new anti-inflammatory agent, selectively inhibits prostaglandin G/H synthase/cyclooxygenase (COX-2) activity in vitro. Prostaglandins, 47, 55-59, 1994.
    • (1994) Prostaglandins , vol.47 , pp. 55-59
    • Futaki, N.1    Takahashi, S.2    Yokoyama, M.3    Arai, I.4    Higuchi, S.5    Otomo, S.6
  • 16
    • 0037192463 scopus 로고    scopus 로고
    • The endocrine disruptor nonylphenol preferentially blocks cyclooxygenase-1
    • Fujimoto, Y., Sakuma, S., Inoue, T., Uno, E., and Fujita, T.: The endocrine disruptor nonylphenol preferentially blocks cyclooxygenase-1. Life Sci., 70, 2209-2214, 2002.
    • (2002) Life Sci , vol.70 , pp. 2209-2214
    • Fujimoto, Y.1    Sakuma, S.2    Inoue, T.3    Uno, E.4    Fujita, T.5
  • 17
    • 0018976320 scopus 로고
    • Evidence for a perxode-initiated free radical mechanism of prostaglandin biosynthesis
    • Hemler, M.E. and Lands, W.E.M.: Evidence for a perxode-initiated free radical mechanism of prostaglandin biosynthesis. J. Biol. Chem., 255, 6253-6261, 1980.
    • (1980) J. Biol. Chem , vol.255 , pp. 6253-6261
    • Hemler, M.E.1    Lands, W.E.M.2
  • 18
    • 0015818768 scopus 로고
    • Isolation and properties of intermediates in prostaglandin biosynthesis
    • Nugteren, D.H. and Hazelhof, E.: Isolation and properties of intermediates in prostaglandin biosynthesis. Biochim. Biophys. Acta, 326, 448-461, 1973.
    • (1973) Biochim. Biophys. Acta , vol.326 , pp. 448-461
    • Nugteren, D.H.1    Hazelhof, E.2
  • 19
    • 0021813370 scopus 로고
    • Metabolism of eicosapentaenoic acid by aorta: Formation of a novel 13-hydroxylated prostaglandin
    • Powell, W.S. and Gravelle, F.: Metabolism of eicosapentaenoic acid by aorta: formation of a novel 13-hydroxylated prostaglandin. Biochim. Biophys. Acta, 835, 201-211, 1985.
    • (1985) Biochim. Biophys. Acta , vol.835 , pp. 201-211
    • Powell, W.S.1    Gravelle, F.2
  • 20
    • 0033575249 scopus 로고    scopus 로고
    • Hydroperoxide dependence and cooperative cyclooxygenase kinetics in prostaglandin H synthase-1 and -2
    • Chen, W., Pawelek, T.R., and Kulmacz, R.J.: Hydroperoxide dependence and cooperative cyclooxygenase kinetics in prostaglandin H synthase-1 and -2. J. Biol. Chem., 274, 20301-20306, 1999.
    • (1999) J. Biol. Chem , vol.274 , pp. 20301-20306
    • Chen, W.1    Pawelek, T.R.2    Kulmacz, R.J.3
  • 21
    • 33745981772 scopus 로고    scopus 로고
    • Divergent cyclooxygenase responses to fatty acid structure and peroxide level in fish and mammalian prostaglandin H synthases
    • Liu, W., Gao, D., Oh, S.F., Serhan, C.N., and Kulmacz, R.J.: Divergent cyclooxygenase responses to fatty acid structure and peroxide level in fish and mammalian prostaglandin H synthases. FASEB J., 20, 1097-1108, 2006.
    • (2006) FASEB J , vol.20 , pp. 1097-1108
    • Liu, W.1    Gao, D.2    Oh, S.F.3    Serhan, C.N.4    Kulmacz, R.J.5
  • 23
    • 0020691373 scopus 로고
    • Lipid composition and cholesterol esterifying activity in microsomal preparations of porcine coronary arteries and heart tissue
    • Cho, B.H.: Lipid composition and cholesterol esterifying activity in microsomal preparations of porcine coronary arteries and heart tissue. Biochem. Med., 29, 64-73, 1983.
    • (1983) Biochem. Med , vol.29 , pp. 64-73
    • Cho, B.H.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.