Lipopolysaccharide-induced DNA damage is greatly reduced in rats treated with the pineal hormone melatonin

被引:55
作者
Sewerynek, E
Ortiz, GG
Reiter, RJ
Pablos, MI
Melchiorri, D
Daniels, WMU
机构
[1] UNIV TEXAS, HLTH SCI CTR, DEPT CELLULAR & STRUCT BIOL, SAN ANTONIO, TX 78284 USA
[2] UNIV LODZ, SCH MED, DEPT THYROIDOL, PL-91425 LODZ, POLAND
[3] IMSS, CIBO, GUADALAJARA, JALISCO, MEXICO
[4] UNIV VALLADOLID, DEPT BIOCHEM & MOL BIOL & PHYSIOL, VALLADOLID, SPAIN
关键词
melatonin; LPS; micronuclei; bone marrow; peripheral blood;
D O I
10.1016/0303-7207(95)03742-X
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The ability of melatonin to influence lipopolysaccharide (LPS)-induced genotoxicity was tested using micronuclei as an index in both bone marrow and peripheral blood cells of rats. LPS was given as a single dose of 10 mg/kg. Melatonin (5 mg/kg) was injected prior to LPS administration and thereafter at 6 h intervals to the conclusion of the study (72 h). The number of micronucleated polychromatic erythrocytes increased significantly after LPS administration both in cells from peripheral blood and bone marrow. Melatonin administration to LPS-treated rats highly significantly reduced micronuclei formation in both peripheral blood and bone marrow cells beginning at 24 h after LPS administration and continuing to the end of the study. In blood the increase in micronuclei formation was time-dependent in LPS-treated rats with peak values being reached at 36-48 h. The ability of melatonin to reduce LPS-related genotoxicity is likely related to its antioxidant activity.
引用
收藏
页码:183 / 188
页数:6
相关论文
共 63 条
  • [1] STRUCTURAL DAMAGE TO LYMPHOCYTE NUCLEI BY H2O2 OR GAMMA-IRRADIATION IS DEPENDENT ON THE MECHANISM OF OH RADICAL PRODUCTION
    ALLAN, IM
    VAUGHAN, ATM
    MILNER, AE
    LUNEC, J
    BACON, PA
    [J]. BRITISH JOURNAL OF CANCER, 1988, 58 (01) : 34 - 37
  • [2] MELATONIN STIMULATES BRAIN GLUTATHIONE-PEROXIDASE ACTIVITY
    BARLOWWALDEN, LR
    REITER, RJ
    ABE, M
    PABLOS, M
    MENENDEZPELAEZ, A
    CHEN, LD
    POEGGELER, B
    [J]. NEUROCHEMISTRY INTERNATIONAL, 1995, 26 (05) : 497 - 502
  • [3] SUPEROXIDE ANION GENERATION IN THE LIVER DURING THE EARLY STAGE OF ENDOTOXEMIA IN RATS
    BAUTISTA, AP
    MESZAROS, K
    BOJTA, J
    SPITZER, JJ
    [J]. JOURNAL OF LEUKOCYTE BIOLOGY, 1990, 48 (02) : 123 - 128
  • [4] SUPEROXIDE ANION GENERATION BY INSITU PERFUSED-RAT-LIVER - EFFECT OF INVIVO ENDOTOXIN
    BAUTISTA, AP
    SPITZER, JJ
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1990, 259 (06): : G907 - G912
  • [5] APPARENT HYDROXYL RADICAL PRODUCTION BY PEROXYNITRITE - IMPLICATIONS FOR ENDOTHELIAL INJURY FROM NITRIC-OXIDE AND SUPEROXIDE
    BECKMAN, JS
    BECKMAN, TW
    CHEN, J
    MARSHALL, PA
    FREEMAN, BA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (04) : 1620 - 1624
  • [6] BECKMAN JS, 1994, ANN NY ACAD SCI, V738, P69
  • [7] REACTIVE OXYGEN SPECIES INDUCE ANTIGENIC CHANGES IN DNA
    BLOUNT, S
    GRIFFITHS, HR
    LUNEC, J
    [J]. FEBS LETTERS, 1989, 245 (1-2): : 100 - 104
  • [8] DNA STRAND SCISSION BY ENZYMICALLY GENERATED OXYGEN RADICALS
    BRAWN, K
    FRIDOVICH, I
    [J]. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1981, 206 (02) : 414 - 419
  • [9] EMERIT I, 1985, Journal of Free Radicals in Biology and Medicine, V1, P51, DOI 10.1016/0748-5514(85)90029-7
  • [10] THE IN-VIVO RAT MICRONUCLEUS TEST - INTEGRATION WITH A 14-DAY STUDY
    GARRIOTT, ML
    BRUNNY, JD
    KINDIG, DEF
    PARTON, JW
    SCHWIER, LS
    [J]. MUTATION RESEARCH-GENETIC TOXICOLOGY, 1995, 342 (1-2): : 71 - 76