Studies of structure-activity relationship of nitroxide free radicals and their precursors as modifiers against oxidative damage

被引:162
作者
Krishna, MC
DeGraff, W
Hankovszky, OH
Sár, CP
Kálai, T
Jeko, J
Russo, A
Mitchell, JB
Hideg, K
机构
[1] Univ Pecs, Inst Organ & Med Chem, H-7643 Pecs, Hungary
[2] NCI, Radiat Biol Branch, Bethesda, MD 20892 USA
[3] ICN Alkaloida Co Ltd, H-4440 Tiszavasvari, Hungary
关键词
D O I
10.1021/jm9802160
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The protective effects of stable nitroxides, as well as their hydroxylamine and amine precursors, have been tested in Chinese hamster V79 cells subjected to H2O2 exposure at fixed concentration or exposure to ionizing radiation. Cytotoxicity was evaluated by monitoring the viability of the cells assessed by the clonogenic assay. The compounds tested at fixed concentration varied in terms of ring size, oxidation state, and ring substituents. Electrochemical studies were carried out to measure the redox midpoint potentials. The studies show that in the case of protection against H2O2 exposure, the protection was determined by the ring size, oxidation state, and redox midpoint potentials. In general the protection factors followed the order nitroxides > hydroxylamines > amines. Both the six-membered ring nitroxides and substituted five-membered ring nitroxides were efficient protectors. For six-membered ring nitroxides, the compounds exhibiting the lowest midpoint potentials exhibited maximal protection. In the case of X-radiation, nitroxides were the most protective though some hydroxylamines were also efficient. The amines were in some cases found to sensitize the toxicity of aerobic radiation exposure. The protection observed by the nitroxides was not dependent on the ring size. However, the ring substituents had significant influence on the protection. Compounds containing a basic side chain were found to provide enhanced protection. The results in this study suggest that these compounds are novel antioxidants which can provide cytoprotection in mammalian cells against diverse types of oxidative insult and identify structural determinants optimal for protection against individual types of damage.
引用
收藏
页码:3477 / 3492
页数:16
相关论文
共 51 条
[1]   NITROXYL SPIN LABEL CONTRAST ENHANCERS FOR MAGNETIC-RESONANCE IMAGING - STUDIES OF ACUTE TOXICITY AND MUTAGENESIS [J].
AFZAL, V ;
BRASCH, RC ;
NITECKI, DE ;
WOLFF, S .
INVESTIGATIVE RADIOLOGY, 1984, 19 (06) :549-552
[2]   THIOL UPTAKE BY CHINESE-HAMSTER V79-CELLS AND AEROBIC RADIOPROTECTION AS A FUNCTION OF THE NET CHARGE ON THE THIOL [J].
AGUILERA, JA ;
NEWTON, GL ;
FAHEY, RC ;
WARD, JF .
RADIATION RESEARCH, 1992, 130 (02) :194-204
[3]  
Bacq Z.M., 1965, CHEM PROTECTION IONI, P263
[4]   REDUCTION AND DESTRUCTION RATES OF NITROXIDE SPIN PROBES [J].
BELKIN, S ;
MEHLHORN, RJ ;
HIDEG, K ;
HANKOVSKY, O ;
PACKER, L .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1987, 256 (01) :232-243
[5]  
BUMP EA, 1997, BURGERS MED CHEM DRU, V4, P3
[6]   HYDROPEROXIDE METABOLISM IN MAMMALIAN ORGANS [J].
CHANCE, B ;
SIES, H ;
BOVERIS, A .
PHYSIOLOGICAL REVIEWS, 1979, 59 (03) :527-605
[7]   ABSOLUTE RATE CONSTANTS FOR THE REACTIONS OF SOME CARBON-CENTERED RADICALS WITH 2,2,6,6-TETRAMETHYLPIPERIDINE-N-OXYL [J].
CHATEAUNEUF, J ;
LUSZTYK, J ;
INGOLD, KU .
JOURNAL OF ORGANIC CHEMISTRY, 1988, 53 (08) :1629-1632
[8]   SYNTHESIS OF NOVEL, HIGHLY REACTIVE 1-OXYL-2,2,6,6-TETRAMETHYL-1,2,5,6-TETRAHYDROPYRIDINE DERIVATIVES [J].
CSEKO, J ;
HANKOVSZKY, HO ;
HIDEG, K .
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1985, 63 (04) :940-943
[9]   NITRONES .1. CYCLOADDITION OF UNSYMMETRICAL OLEFINS TO 1-PYRROLINE 1-OXIDES [J].
DELPIERRE, GR ;
LAMCHEN, M .
JOURNAL OF THE CHEMICAL SOCIETY, 1963, (OCT) :4693-&
[10]   Quantification of superoxide radicals and peroxynitrite in vascular cells using oxidation of sterically hindered hydroxylamines and electron spin resonance [J].
Dikalov, S ;
Skatchkov, M ;
Fink, B ;
Bassenge, E .
NITRIC OXIDE-BIOLOGY AND CHEMISTRY, 1997, 1 (05) :423-431