Oxidative stress parameters and anti-apoptotic response to hydroxyl radicals in fish erythrocytes: Protective effects of glutamine, alanine, citrulline and proline

被引:82
作者
Li, Hua-Tao [1 ,2 ,3 ]
Feng, Lin [1 ,2 ,3 ]
Jiang, Wei-Dan [1 ,2 ,3 ]
Liu, Yang [1 ,2 ,3 ]
Jiang, Jun [1 ,2 ,3 ]
Li, Shu-Hong [1 ]
Zhou, Xiao-Qiu [1 ,2 ,3 ]
机构
[1] Sichuan Agr Univ, Inst Anim Nutr, Chengdu 611130, Sichuan, Peoples R China
[2] Sichuan Agr Univ, Fish Nutr & Safety Prod Univ Key Lab Sichuan Prov, Chengdu 611130, Sichuan, Peoples R China
[3] Sichuan Agr Univ, Minist Educ, Key Lab Anim Dis Resistance Nutr, Chengdu 611130, Sichuan, Peoples R China
基金
美国国家科学基金会;
关键词
Fish erythrocyte; Apoptosis; Glutamine; Alanine; Citrulline; Proline; INTESTINAL EPITHELIAL-CELLS; TROUT GILL CELLS; LIPID-PEROXIDATION; CYPRINUS-CARPIO; HYDROGEN-PEROXIDE; REACTIVE OXYGEN; AMINO-ACID; ANTIOXIDANT STATUS; AQUATIC ORGANISMS; DNA-DAMAGE;
D O I
10.1016/j.aquatox.2012.11.005
中图分类号
Q17 [水生生物学];
学科分类号
071004 ;
摘要
The present study explored the protective effects of glutamine (Gln), alanine (Ala), citrulline (Cit) and proline (Pro) on hydroxyl radical ((OH)-O-center dot)-induced apoptosis in isolated carp erythrocytes. Hydroxyl radicals were generated by ferrous ion (Fe2+)-mediated decomposition of hydrogen peroxide (H2O2) (Fenton reaction). In order to select an optimal (OH)-O-center dot concentration to induce apoptosis, cultures were treated with different concentrations of FeSO4/H2O2 (0 mu M/0 mu M-50 mu M/25 mu M). The results showed that exposure to FeSO4/H2O2 (0 mu M/0 mu M-40 mu M/20 mu M) increased apoptosis in a dose-dependent manner. Moreover, apoptosis was at its highest level at 40 mu M FeSO4/20 mu M H2O2. We then examined the cytoprotective effects of Gln, Ala, Cit, Pro or the combination of Ala, Cit and Pro under conditions of apoptosis. Carp erythrocytes were treated with the substances listed above in the presence of 40 mu M FeSO4/20 mu M H2O2 for 9 h. The controls were grown in Gln, Ala, Cit, Pro-free culture medium. The results showed that Gln, Ala, Cit, Pro and the combination of Ala, Cit and Pro effectively protected against annexin binding, decrease of forward scatter and DNA fragmentation in carp erythrocytes induced by (OH)-O-center dot. Furthermore, Gln, Ala, Cit, Pro and the combination of Ala, Cit and Pro effectively blocked (OH)-O-center dot-stimulated erythrocyte hemolysis, reduced the increase of superoxide anion and H2O2 concentrations, inhibited the formation of malondialdehyde, protein carbonyls and met-hemoglobin, and prevented the decrease of superoxide dismutase, catalase and glutathione peroxidase activities and glutathione content in carp erythrocytes induced by (OH)-O-center dot. In addition, the results suggest that the combination of Ala, Cit and Pro produces a greater anti-apoptotic and anti-oxidative effect than their individual effects at the same concentrations. Taken together, the results showed that (OH)-O-center dot induces apoptosis and oxidative damage in carp erythrocytes. In addition to inhibiting apoptosis, Gln, Ala, Cit, Pro and the combination of Ala, Cit and Pro protected carp erythrocytes against oxidative damage induced by (OH)-O-center dot, which may be a major factor in the protection of erythrocytes from apoptosis. (c) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:169 / 179
页数:11
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