Antitumor activities of vanadium(IV), manganese(IV), iron(III), cobalt(II) and copper(II) complexes of 2-methylaminopyridine

被引:36
作者
El-Naggar, MM [1 ]
El-Waseef, AM
El-Halafawy, KM
El-Sayed, IH
机构
[1] Univ Mansoura, Dept Chem, Fac Sci, Div Biochem, Mansoura, Egypt
[2] Menoufia Univ, Inst Genet Engn & Biotechnol, Menoufia, Egypt
[3] Coll Pharm, Dept Med Chem, Little Rock, AR 72205 USA
关键词
antitumor activity; transition metal complexes; Ehrlich ascites carcinoma cells; 2-methylaminopyridine;
D O I
10.1016/S0304-3835(98)00213-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The effect of Cu(II), Mn(IV), Fe(III), V(IV) and Co(II) complexes of 2-methylaminopyridine (L) having superoxide dismutase (SOD)-like activities on Ehrlich ascites carcinoma (EAC) cells was studied. Each of these complexes was intraperitoneally administered (10 mg/kg body weight for 9 days) to Swiss albino mice implanted intraperitoneally with 1 x 10(6) EAC cells. Six days after the last treatment the EAC cells were harvested using a heparinized syringe. The volume of EAC cells and EAC cell viability as well as changes in the levels of tumor cell enzyme activities of SOD, catalase, glutathione peroxidase (GSH-Px), glutathione reductase (GSH-R) and glucose-6-phosphate dehydrogenase (G6PD) were tested to examine the antitumor effects of these complexes. Both tumor volume and tumor cell viability were significantly lowered in complex-treated mice. After tumor transplantation and treatment with the complexes, the activities of GSH-Px and GSH-R were significantly lowered while SOD and G6PD activities were increased in EAC cells compared to their levels in EAC cells harvested from saline-treated mice. (C) 1998 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:71 / 76
页数:6
相关论文
共 16 条
[1]  
BERTINI I, 1994, BIOINORG CHEM, P455
[2]  
BEUTLER E, 1973, RED CELL METABOLISM, P66
[3]  
BOYSE E A, 1964, Methods Med Res, V10, P39
[4]  
DAS AK, 1990, TXB MED ASPECTS BIOI, P70
[5]   SUPEROXIDE-DISMUTASE ACTIVITY IN LEUKOCYTES [J].
DECHATELET, LR ;
MCCALL, CE ;
MCPHAIL, LC ;
JOHNSTON, RB .
JOURNAL OF CLINICAL INVESTIGATION, 1974, 53 (04) :1197-1201
[6]   ENZYME-BASED THEORY OF OBLIGATE ANAEROBIOSIS - PHYSIOLOGICAL FUNCTION OF SUPEROXIDE DISMUTASE [J].
MCCORD, JM ;
KEELE, BB ;
FRIDOVICH, I .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1971, 68 (05) :1024-+
[7]  
OBERLEY LW, 1983, J NATL CANCER I, V71, P1089
[8]  
OBERLEY LW, 1982, PATHOLOGY OXYGEN, P207
[9]  
OBERLEY LW, 1984, AGENTS ACTIONS, V15, P335
[10]  
PETKAU A, 1977, RES COMMUN CHEM PATH, V17, P125