Free radical scavenging and copper chelation: A potentially beneficial action of captopril

被引:21
作者
Tamba, M
Torreggiani, A
机构
[1] Ist FRAE, I-40129 Bologna, Italy
[2] Ist Nazl MTCI CNR, Area Ric, I-40129 Bologna, Italy
关键词
captopril; captopril/copper complexes; hydroxyl radicals; peroxyl radicals; Raman spectroscopy; pulse radiolysis;
D O I
10.1080/10715760000300211
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Captopril (CpSH), an angiotensin converting enzyme (ACE) inhibitor, is reported to provide protection against free-radical mediated damage. The purpose of this study was to investigate, by means of pulse radiolysis technique, the behaviour of CpSH towards radiation-induced radicals in the absence and in the presence of copper(II) ions, which can play a relevant role in the metal catalysed generation of reactive oxygen species. The results indicate that the -SH group is crucial in determining the radical scavenging action of CpSH and the nature of the resulting CpSH transient products in the absence or in the presence of oxygen. In the presence of Cu(II), the -SH group is still involved in the biological action of the molecule participating both in the one-electron reduction of Cu(II) with formation of CpSSCp, and in Cu(I) chelation. This conclusion is supported by the Raman spectroscopic data which allow to identify the CpSH sites involved in the copper complex at different pH. These results suggest that CpSH may potentially inhibit oxidative damage both through free radical scavenging and metal chelation. Considering the low CpSH concentration in vivo, the metal chelation mechanism, more than the direct radical scavenging, could play the major role in moderating the toxicological effects of free radicals.
引用
收藏
页码:199 / 211
页数:13
相关论文
共 45 条
[11]   BIOLOGICAL ANALOGS - SPECTROSCOPIC CHARACTERISTICS OF MERACAPTO-COPPER(II) AND DISULFIDE-COPPER(II) COORDINATION IN RELATION TO TYPE-I PROTEINS [J].
DOWNES, JM ;
WHELAN, J ;
BOSNICH, B .
INORGANIC CHEMISTRY, 1981, 20 (04) :1081-1086
[12]   ELECTRON-PARAMAGNETIC RESONANCE STUDY OF THE COMPLEX FORMED BETWEEN COPPER AND 1-[2(S)-3-MERCAPTO-2-METHYLPROPIONYL]-L-PROLINE (CAPTOPRIL) IN SOLID AND AQUEOUS-SOLUTION [J].
EVANS, JC ;
MORRIS, CR ;
REES, SB ;
ROWLANDS, CC ;
WILLIAMS, DR .
MAGNETIC RESONANCE IN CHEMISTRY, 1989, 27 (03) :227-232
[13]   Different effects of thiol and nonthiol ACE inhibitors on copper-induced lipid and protein oxidative modification [J].
Fernandes, AC ;
Filipe, PM ;
Freitas, JP ;
Manso, CF .
FREE RADICAL BIOLOGY AND MEDICINE, 1996, 20 (04) :507-514
[14]  
FREEDMAN JH, 1989, J BIOL CHEM, V264, P5598
[15]   DIRECT EVIDENCE FOR INHIBITION OF FREE-RADICAL FORMATION FROM CU(I) AND HYDROGEN-PEROXIDE BY GLUTATHIONE AND OTHER POTENTIAL LIGANDS USING THE EPR SPIN-TRAPPING TECHNIQUE [J].
HANNA, PM ;
MASON, RP .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1992, 295 (01) :205-213
[16]   THE BINDING OF METAL-IONS BY CAPTOPRIL (SQ 14225) .1. COMPLEXATION OF ZINC(II), CADMIUM(II) AND LEAD(II) [J].
HUGHES, MA ;
SMITH, GL ;
WILLIAMS, DR .
INORGANICA CHIMICA ACTA-BIOINORGANIC CHEMISTRY, 1985, 107 (04) :247-252
[17]   CAPTOPRIL DOES NOT SCAVENGE SUPEROXIDE - CAPTOPRIL PREVENTS O2 PRODUCTION BY CHELATING COPPER [J].
JAY, D ;
CUELLAR, A ;
ZAMORANO, R ;
MUNOZ, E ;
GLEASON, R .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1991, 290 (02) :463-467
[18]   PROTECTIVE EFFECTS OF SULFHYDRYL-CONTAINING ANGIOTENSIN CONVERTING ENZYME-INHIBITORS AGAINST FREE-RADICAL INJURY IN ENDOTHELIAL-CELLS [J].
MAK, IT ;
FREEDMAN, AM ;
DICKENS, BF ;
WEGLICKI, WB .
BIOCHEMICAL PHARMACOLOGY, 1990, 40 (09) :2169-2175
[19]  
MARTIN MFR, 1984, LANCET, V1, P1325
[20]  
MCCORD JM, 1985, NEW ENGL J MED, V312, P159