Protective effect of melatonin on naphthalene‐induced oxidative stress and DNA damage in cultured macrophage J774A.1 cells

被引:0
作者
M. Bagchi
J. Balmoori
X. Ye
D. Bagchi
S.D. Ray
S.J. Stohs
机构
[1] Creighton University School of Pharmacy and Allied Health Professions,AMS College of Pharmacy
[2] Long Island University,undefined
来源
Molecular and Cellular Biochemistry | 2001年 / 221卷
关键词
naphthalene; oxidative stress; J774A.1 macrophage cells; melatonin; cell viability; lipid peroxidation; cytochrome ; reduction; DNA fragmentation;
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中图分类号
学科分类号
摘要
Naphthalene is a bicyclic aromatic compound that is widely used in various domestic and commercial applications. Previous studies in our laboratory have demonstrated enhanced production of reactive oxygen species, lipid peroxidation and DNA fragmentation in both in vitro and in vivo models following treatment with naphthalene. Melatonin (N‐acetyl‐5‐methoxytryptamine), an indole hormone, is the chief secretory product of the pineal gland and is an efficient free radical scavenger and antioxidant, both in vitro and in vivo. In this study, we have investigated the ability of 1 mM melatonin to protect against naphthalene-induced oxidative stress and DNA damage in cultured macrophage J774A.1 cells. No significant changes were observed when these macrophage cells were treated with 100 μM naphthalene. Approximately 2.0‐, 4.2‐ and 4.4‐fold increases in cytochrome c reduction were observed at 200, 400 and 500 mM concentrations of naphthalene, demonstrating the increased production of superoxide anion. At 24 h, lipid peroxidation increased by approximately 1.4‐, 2.1‐ and 2.2‐fold following treatment of these cells with 200, 400 and 500 mM concentrations of naphthalene, respectively, while 1.6‐, 2.8‐ and 2.8‐fold increases in DNA fragmentation were observed at these same concentrations. Two hour pretreatment of these cultured cells with 1 mM melatonin provided approximately 26–44% decreases in lipid peroxidation, superoxide anion production and DNA fragmentation in cells treated with 400 and 500 μM naphthalene. Cellular viability decreased significantly when cells were incubated with concentrations of naphthalene greater than 100 μM, while preincubation with melatonin significantly increased the cellular viability. These results demonstrate that naphthalene may induce toxic manifestations by enhanced production of reactive oxygen free radicals, resulting in lipid peroxidation and DNA damage, while preincubation with melatonin significantly suppressed cytoxicity in J774A.1 macrophage cells.
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页码:49 / 55
页数:6
相关论文
共 149 条
[1]  
Bagchi M(1998)Naphthalene-induced oxidative stress and DNA damage in cultured macrophage J774A.1 cells Free Rad Biol Med 25 137-143
[2]  
Bagchi D(1990) metabolism of isomeric naphthalene oxide glutathione conjugates Dispos 18 183-189
[3]  
Balmoori J(1994)Reactive naphthalene metabolite binding to hemoglobin and albumin Fund Appl Toxicol 22 26-33
[4]  
Ye X(1996)Naphthalene-induced oxidative stress in rats and the protective effects of vitamin E succinate Free Rad Biol Med 21 577-590
[5]  
Stohs SJ(1995)Protective effects of free radical scavengers and antioxidants against smokeless tobacco extract (STE)-induced oxidative stress in macrophage J774A.1 cell cultures Arch Environ Contam Toxicol 29 424-428
[6]  
Buonarati M(1976)Naphthalene cataract development Doc Opthal 3 323-332
[7]  
Jones AD(1989)Cataractogenicity and bioactivation of naphthalene derivatives in lens culture and Lens Eye Toxicol Res 6 203-209
[8]  
Buckpitt AR(1999)Augmentation of indices of oxidative damage in life long melatonin-deficient rats Mech Aging Dev 110 157-173
[9]  
Cho M(1999)The oxidant/antioxidant network: Role of melatonin Biol Signals Recept 8 56-63
[10]  
Jedrychowski R(1997)Melatonin in relation to cellular antioxidative defense mechanisms Horm Metal Res 8 363-372