Fast repair of hydroxy radical purine deoxynucleotide adducts by phenylpropanoid glycosides and their derivatives from Chinese herbs

Biochimica et Biophysica Acta - General Subjects

Volumn 1472, Issue 1-2, 1999, Pages 115-127

  Shi, Yimin ^a   Lin, Weizheng ^c   Fan, Botao ^d   Jia, Zhongjian ^b   Yao, Side ^c   Kang, Jiuhong ^c   Wang, Wengfeng ^c   Zheng, Rongliang ^a  

^a LANZHOU UNIVERSITY   (China)

^b LANZHOU UNIVERSITY   (China)

^c Shanghai Institute of Nuclear Research AcademiaSinica   (China)

^d University of Paris   (France)

Author keywords

DNA damage; Fast repair; Hydroxyl radical; Phenylpropanoid glycoside; Pulse radiolysis

Indexed keywords

DEOXYRIBONUCLEOTIDE; GLYCOSIDE; HYDROXYL RADICAL; NITROUS OXIDE; OXYGEN RADICAL;

AGING; ARTICLE; CANCER; CHINESE HERB; CONTROLLED STUDY; DEGENERATIVE DISEASE; DNA DAMAGE; DNA REPAIR; NONHUMAN; PRIORITY JOURNAL; PULSE RADIOLYSIS;

DNA ADDUCTS; DNA REPAIR; DRUGS, CHINESE HERBAL; GLYCOSIDES; HYDROXYL RADICAL; PHENOLS; PHENYLPROPIONATES;

EID: 0032828393     PISSN: 03044165     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0304-4165(99)00111-7     Document Type: Article

References (50)

1. Lesko S.A., Trapis L., Zheng R.L. Somatic mutation, DNA damage and cytotoxicity induced by benzo(a)pyrenedione/benzo(a)pyrenediol redox coupled in cultured mammalian cell. Mutat. Res. 161:1988;173-180.
2. S.L. Lesko, P.O.P. Ts'o, S.U. Yang, R.L. Zheng, Benzo(a)-pyrene radicals and oxygen radical involvement in DNA damage, cellular toxicity and carcinogenesis, in: D.C.H. McBrien, T.F. Slater (Eds.), Free Radicals, Lipid Peroxidation and Cancer, Academic Press, New York, 1982, pp. 401-420.
3. Zheng R.L., Lesko S.A., Ts'o P.O.P. DNA damage induced in mammalian cell by active oxygen species. Sci. China B. 31:1988;57-67.
4. Floyd R.A. Role of oxygen free radicals in carcinogenesis and brain ischemia. FASEB J. 4:1988;2587-2597.
5. S.J. Klebanoff, in: J.I. Gallin, I.M. Goldstein, I.M.R. Snyderman (Eds.), Inflammation: Basic Principles and Clinical Correlates, Raven Press, New York, 1988, pp. 391-444.
6. N.L. Oleinick, S.M. Chio, Radiation Research: Chromatin and Nuclear Structural Factors which Modify the Radiosensitivity of DNA, vol. II, Academic Press, San Diego, CA, 1992, p. 149.
7. - and OH adducts. Chem. Rev. 89:1989;503-520.
8. Gajewski E., Rao G., Neckerdien Z., Dizdaroglu M. Modification of DNA bases in mammalian chromatin by radiation-generated free radicals. Biochemistry. 29:1990;7876-7882.
9. K.J.A. Davies, A.G. Wiese, A. Sevanian, E.H. Kim, Repair system in oxidative stress, in: Molecular Biology of Aging, Liss, New York, 1990, pp. 123-141.
10. S.S. Wallace, Oxidative damage to DNA and its repair, in: J.G. Scandalios (Ed.), Oxidative Stress and the Molecular Biology of Antioxidant Defenses, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, 1997, pp. 49-90.
11. B.N. Ames, M.K. Shigenaga, DNA damage by endogenous oxidants and mitogenesis as cause of aging and cancer, in: J.G. Scandalies (Ed.), Molecular Biology of Free Radical Scavenging Systems, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, 1992, pp. 1-22.
12. T.G. Newcomb, L.A. Loeb, Oxidative DNA damage and mutagenesis, in: J.A. Nickoloff, M.F. Hoekstra (Eds.), DNA Damage and Repair, vol. 1: DNA Repair in Prokaryotes and Lower Eukaryotes, Humana Press, Totowa, 1998, pp. 65-84.
13. Loeb L.A. Endogenous carcinogenesis: molecular oncology into the twenty-first century-presidential address. Cancer Res. 49:1989;5489-5496.
14. Zhou C.Y., Zheng R.L. Phenolic compounds and an analog as superoxide anions scavengers and antioxidants. Biochem. Pharmacol. 42:1991;1177-1179.
15. O'Neill P. Pulse radiolytic study of the interaction of thiols and ascorbate with OH adducts of dGMP and dG: implications for DNA repair processes. Radiat. Res. 96:1983;198-210.
16. O'Neill P., Chapman P.W. Potential repair of free radical adduct on deoxy-GMP and deoxy-guanosine by series of reductants: a pulse radiolysis study. Int. J. Radiat. Biol. 47:1985;71-81.
17. Jiang Y., Yao S.D., Lin N.Y. Fast repair of oxidizing OH radical adduct of dGMP by hydroxycinnamic acid derivatives: a pulse radiolytic study. Radiat. Phys. Chem. 49:1997;447-450.
18. Jiangsu New Medical College, in: The Chinese Medicine Dictionary, Shanghai People's Publishing House, Shanghai, 1977, pp. 276, 286, 487, and 2674.
19. Kong B., Dustmann J.H. The caffeoylics as a new family of natural antiviral compounds. Naturwissenschaften. 72:1985;659-661.
20. Pettit G.R., Numata A., Takemura T., Ode R.H., Narula A.S., Schmidt J.M., Gragg G.M., Pase C.P. Antineoplastic agents, 107, isolation of acteoside and isoactcoside from Gastilleja linariaefolia. J. Nat. Prod. 53:1990;456-458.
21. Mahato S.B., Sahu N.P., Roy S.K., Sharma O.P. Potential antitumor agents from Lantana camara: structures of flavonoid, and phenylpropanoid glycosides. Tetrahedron. 50:1994;9439-9446.
22. Miyase T., Ishion M., Akahori C., Ueno A., Ohkawa Y., Tanizawa H. Phenylethanoid glycosides from Plantago asiatica. Phytochemistry. 30:1991;2015-2018.
23. Pan N., Hori H. Antioxidant action of acteoside and its analogs on lipid peroxidation. Redox Rep. 2:1996;149-154.
24. Cano E., Veige M., Jimenez C., Riguera R. Pharmacological effects of three phenylpropanoid glycosides from Mussatia. Planta Med. 56:1990;24-26.
25. Jimenez C., Villaverde M.C., Riguera R., Castedo L., Stermuz E. Triterpene glycosides from Mussatia species. Phytochemistry. 8:1989;2773-2776.
26. Li J., Zheng R.L., Liu Z.M., Jia Z.J. Scavenging effects of phenylpropanoid glycosides on superoxide and its antioxidation effect. Acta Pharmacol. Sin. 13:1992;427-430.
27. Wang P.F., Zheng R.L., Li J. Inhibition of autooxidation of linoleic acid by phenylpropanoid glycosides from Pedicularis in micelles. Chem. Phys. Lipids. 63:1993;37-40.
28. Li J., Wang P.F., Zheng R.L., Liu Z.M., Lia Z.J. Protection of phenylpropanoid glycosides from Pedicularis against oxidative hemolysis in vitro. Planta Med. 59:1993;315-317.
29. Li J., Ge R.C., Zheng R.L., Liu Z.M., Jia Z.J. Antioxidative and chelating activities of phenylpropanoid glycosides from Pedicularis strata. Acta Pharmacol. Sin. 18:1997;77-80.
30. Li J., Zheng R.L., Liu Z.M., Jia Z.J. Antitumour effects of phenylpropanoid glycosides. Chin. Pharm. J. 30:1995;269-271.
31. Wang P.F., Zheng R.L., Gao J.J., Jia Z.J., Wang W.F., Yao S.D., Zhang J.S., Lin N.Y. Reaction of hydroxyl radical with phenylpropanoid glycosides from Pedicularis species: a pules radiolysis study. Sci. China C. 39:1996;154-158.
32. Li J., Zheng Y., Zhou H., Su B.N., Zheng R.L. Differentiation of human gastric adenocarcinoma cell line MGc 80-3 induced by verbascoside. Planta Med. 63:1997;499-502.
33. Li W.Y., Zheng R.L., Su B.N., Jia Z.J., Li H.C., Jiang Y., Yao S.D., Lin N.Y. Repair of dGMP hydroxyl radical adducts by verbascoside via electron transfer: a pulse radiolysis study. Int. J. Radiat. Biol. 69:1996;481-486.
34. Li W.Y., Zou Z.H., Zheng R.L., Wang C.Z., Jia Z.J., Yao S.D., Lin N.Y. Fast repair of thymine-hydroxyl radical adduct by phenylpropanoid glycosides. Radiat. Phys. Chem. 49:1997;429-432.
35. Li W.Y., Zheng R.L., Jia Z.J., Zou Z.H., Lin N.Y. Repair effect of phenylpropanoid glycosides on thymine radical anion induced by pulse radiolysis. Biophys. Chem. 67:1997;281-286.
36. Li W.Y., Zheng R.L., Zhao S.L., Jiang Y., Lin N.Y. Repair effect of thymine radical anion by echinocoside using pulse radiolysis. Sci. China C. 39:1997;544-550.
37. Pharmacopoia of P.R. China, People's Health Publishing House, Beijing, 1995, p. 124.
38. Horacio A.P. Minor aristolochic acids from Aristolochia argentina and mass spectral analysis of aristolochic acids. Phytochemistry. 26:1987;519-529.
39. Li H., Sakagami Y., Marumo S., Chen X.M. Eleven aristolochic acids derivatives from Aristolochia cinnabarina. Phytochemistry. 37:1994;237-239.
40. Jia Z.J., Gao J.J. Phenylpropanoid glycosides from Pedicularis striata pall ssp. arachnoidea. Phytochemistry. 34:1994;1188-1190.
41. Jia Z.J., Gao J.J., Liu Z.M. Iridoid and phenylpropanoid glycosides from Pedicularis plicata Maxim. Ind. J. Chem. 33B:1994;460.
42. Yao S.D., Sheng S.G., Cai J.H., Zhang J.S. Nanosecond pulse radiolysis studies in China. Radiat. Phys. Chem. 46:1995;105-113.
43. K.D. Asmus, Sulfur-centred free radicals, in: O.F. Nygaard, M.G. Simic (Eds.), Radioprotectors and Anticarcinogens, Academic Press, New York, 1983, pp. 23-42.
44. G. Scholes, R.L. Willson, M. Ebert, Pulse radiolysis of aqueous solution of deoxyribonucleotides and of DNA: reaction with hydroxyl radicals, J. Chem. Soc. Chem. Commun. (1969) 17-18.
45. Willson R.L. The reaction of oxygen with radiation-induced free radicals in DNA and related compounds. Int. J. Radiat. Biol. 17:1970;349-358.
46. 4 and Br in aqueous solution. Radiat. Res. 67:1978;1-8.
47. -) in aqueous solution. J. Phys. Chem. Ref. Data. 17:1988;513-518.
48. O'Neill P., Chapman P.W. Potential repair of free radical adduct on deoxy-GMP and deoxy-guanosine by series of reductants: a pulse radiolysis study. Int. J. Radiat. Biol. 47:1985;71-81.
49. O'Neill P., Davies S.F. Pulse radiolytic study of the interaction of nitroxyls with free-radical adducts of purine: consequences for radiosensitization. Int. J. Radiat. Biol. 49:1986;937-940.
50. Yakes F.M., van Houte B. Mitochondrial DNA damage is more extensive and persists longer than nuclear DNA damage in human cells following oxidative stress. Proc. Natl. Acad. Sci. USA. 94:1997;514-519.