Amelioration of radiation-induced oxidative stress and biochemical alteration by SOD model compounds in pre-treated γ-irradiated rats

被引:24
作者
Abou-Seif, MAM
El-Naggar, MM
El-Far, M
Ramadan, M
Salah, N
机构
[1] Univ Mansoura, Fac Sci, Dept Chem, Div Biochem, El Mansura, Egypt
[2] Tanta Univ, Fac Educ, Dept Chem, Tanta, Egypt
关键词
antioxidant enzymes; whole body irradiation; 5 '-nucleatidase; DNA; RNA; AChE; X-IRRADIATION; SUPEROXIDE-DISMUTASE; ZINC ASPARTATE; ACETYLCHOLINESTERASE; PROTECTION; SYNERGISM; PROTEIN; ANION; SKIN;
D O I
10.1016/S0009-8981(03)00192-X
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Introduction: The role of metalloelements in tissue maintenance, function and response to injury offer a new approach to decreasing and/or treating radiation injury. We investigated the roles of CuL2SO4, [MnL2O](2)Cl-4(H2O)(2) and [(VL2O)(VL2 H2O)]Cl-6 complexes (L=2 -methylaminopyridine) of SOD-mimetic activities, in ameliorating the radiation-induced oxidative stress and alterations in some biochemical parameters in liver, kidney, spleen and brain in pretreated female rats exposed to gamma-irradiation. Methods: Both Untreated-rats and rats treated with the above complexes were subjected to whole-body gamma-irradiation (6 Gy). 5'-Nucleotidase (5'-NT), acetylcholinesterase (AChE), adenosne triphosphatase (ATPase), superoxide dismutase (SOD), catalase (CAT) and glutathione reductase (GSSG-R) were assessed as well as liver DNA and RNA contents and total protein concentration were estimated in tissue homogenates of the above organs. The same parameters were assessed in non-irradiated treated rats and normal control rats. Results were compared to irradiated non-treated and normal control rats. Results: Pretreatment of gamma-irradiated rats with Mn(IV) or V(IV) complex produced a significant decrease in liver 5'-NT activity compared to the corresponding value of the untreated irradiated rats. In contrast, liver DNA and RNA contents and brain AChe and ATPase activities were significantly increased in irradiated rat group pre-treated with these metal complexes. Cu II, Mn IV or V IV complex inoculation prior to irradiation of normal rats exhibited a significant increase in SOD, CAT, GSSG-R activities and protein content of liver, kidney, spleen and brain homogenates compared with that of the untreated irradiated rats. The treatment of non-irradiated rats with these complexes produced a highly significant increase in mean activities of SOD and CAT, with no changes in other parameters vs. controls. Conclusions: Cu(II), Mn(IV) and V(IV) 2-methylaminopyridine complexes offer a physiological approach to ameliorate the radiation-induced biochemical alterations. In addition, they provide sufficient protection against radiation injury of radiosensitive tissues. (C) 2003 Elsevier BY. All rights reserved.
引用
收藏
页码:23 / 33
页数:11
相关论文
共 44 条
[11]   A NEW AND RAPID COLORIMETRIC DETERMINATION OF ACETYLCHOLINESTERASE ACTIVITY [J].
ELLMAN, GL ;
COURTNEY, KD ;
ANDRES, V ;
FEATHERSTONE, RM .
BIOCHEMICAL PHARMACOLOGY, 1961, 7 (02) :88-&
[12]  
ELSAYED IH, THESIS MANSOURA U EG
[13]   FURTHER-STUDIES ON SELECTIVE RADIOPROTECTION BY ORGANIC ZINC SALTS AND SYNERGISM OF ZINC ASPARTATE WITH WR-2721 [J].
FLOERSHEIM, GL ;
BIERI, A .
BRITISH JOURNAL OF RADIOLOGY, 1990, 63 (750) :468-475
[14]   PROTECTION AGAINST IONIZING-RADIATION AND SYNERGISM WITH THIOLS BY ZINC ASPARTATE [J].
FLOERSHEIM, GL ;
FLOERSHEIM, P .
BRITISH JOURNAL OF RADIOLOGY, 1986, 59 (702) :597-602
[15]  
HANMEN B, 1990, FUSHE YANJW YU FUSHE, V8, P1
[16]   EFFECTS OF ELECTROACUPUNCTURE ON LEUKOCYTES AND PLASMA-PROTEIN IN THE X-IRRADIATED RATS [J].
HAU, DM .
AMERICAN JOURNAL OF CHINESE MEDICINE, 1984, 12 (1-4) :106-114
[17]   RADIORECOVERY ACTIVITY OF MANGANESE(III)2(II)(MU(3)-O)-(MU-3,5-DIISOPROPYLSALICYLATE)(6) [J].
HENDERSON, TD ;
BURT, RL ;
KAUFMAN, SE ;
WILLINGHAM, WM ;
SORENSON, JRJ .
RADIATION RESEARCH, 1993, 136 (01) :126-129
[18]  
KHASAN S S, 1991, Radiobiologiya, V31, P326
[20]   Radiation sensitivity of an Escherichia coli mutant lacking NADP+-dependent isocitrate dehydrogenase [J].
Lee, SM ;
Koh, HJ ;
Huh, TL ;
Park, JW .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 254 (03) :647-650