The metabolism of sulindac enhances its scavenging activity against reactive oxygen and nitrogen species

被引:56
作者
Fernandes, E [1 ]
Toste, SA [1 ]
Lima, JLFC [1 ]
Reis, S [1 ]
机构
[1] Univ Porto, Fac Farm, Dept Quim Fis, REQUIMTE, P-4050047 Oporto, Portugal
关键词
NSAIDs; sulindac; sulindac sulfide; sulindac sulfone; scavenging activity; reactive oxygen species; reactive nitrogen species; free radicals;
D O I
10.1016/S0891-5849(03)00437-4
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
Sulindac is a sulfoxide prodrug that, in vivo, is converted to the metabolites sulindac sulfide and sulindac sulfone. It is therapeutically used as an anti-inflammatory and analgesic in the symptomatic treatment of acute and chronic rheumatoid arthritis, osteoarthritis, and ankylosing spondylitis. In addition to its anti-inflammatory properties, sulindac and its metabolites have been shown to have an important role in the prevention of colonic carcinogenesis. Although the inhibition of prostaglandin synthesis constitutes the primary mechanism of action of sulindac, it is well known that reactive oxygen species (ROS) and reactive nitrogen species (RNS) are implicated in the pathophysiology of inflammation and cancer. Thus, the aim of this study was to evaluate the scavenging activity of sulindac and its sulfone and sulfide metabolites for an array of ROS (HO., O-2(.-), and HOCl) and RNS ((NO)-N-. and ONOO-) using in vitro systems. The results we obtained demonstrate that the metabolism of sulindac increases its scavenging activity for all RNS and ROS studied, notably with regard to the scavenging of HOCl. These effects may strongly contribute to the anti-inflammatory and anticarcinogenic efficacy that has been shown for sulindac. (C) 2003 Elsevier Inc.
引用
收藏
页码:1008 / 1017
页数:10
相关论文
共 65 条
[31]   ANTIINFLAMMATORY DRUGS - PROTECTION OF A BACTERIAL-VIRUS AS AN INVITRO BIOLOGICAL MEASURE OF FREE-RADICAL ACTIVITY [J].
HILLER, KO ;
HODD, PL ;
WILLSON, RL .
CHEMICO-BIOLOGICAL INTERACTIONS, 1983, 47 (03) :293-305
[32]   Nitric oxide in arthritis [J].
Jang, D ;
Murrell, GAC .
FREE RADICAL BIOLOGY AND MEDICINE, 1998, 24 (09) :1511-1519
[33]   Hydroxyl radical scavenging activity of nonsteroidal anti-inflammatory drugs [J].
Kataoka, M ;
Tonooka, K ;
Ando, T ;
Imai, K ;
Aimoto, T .
FREE RADICAL RESEARCH, 1997, 27 (04) :419-427
[34]   PEROXYNITRITE-MEDIATED OXIDATION OF DIHYDRORHODAMINE-123 [J].
KOOY, NW ;
ROYALL, JA ;
ISCHIROPOULOS, H ;
BECKMAN, JS .
FREE RADICAL BIOLOGY AND MEDICINE, 1994, 16 (02) :149-156
[35]   Nitric oxide and intestinal inflammation [J].
Kubes, P ;
McCafferty, DM .
AMERICAN JOURNAL OF MEDICINE, 2000, 109 (02) :150-158
[36]   CEPHALOSPORINS ARE SCAVENGERS OF HYPOCHLOROUS ACID [J].
LAPENNA, D ;
CELLINI, L ;
DEGIOIA, S ;
MEZZETTI, A ;
CIOFANI, G ;
FESTI, D ;
CUCCURULLO, F .
BIOCHEMICAL PHARMACOLOGY, 1995, 49 (09) :1249-1254
[37]   The sulfide metabolite of sulindac prevents tumors and restores enterocyte apoptosis in a murine model of familial adenomatous polyposis [J].
Mahmoud, NN ;
Boolbol, SK ;
Dannenberg, AJ ;
Mestre, JR ;
Bilinski, RT ;
Martucci, C ;
Newmark, HL ;
Chadburn, A ;
Bertagnolli, MM .
CARCINOGENESIS, 1998, 19 (01) :87-91
[38]   DIFFERENT SELECTIVITIES OF OXIDANTS DURING OXIDATION OF METHIONINE RESIDUES IN THE ALPHA-1-PROTEINASE INHIBITOR [J].
MAIER, KL ;
MATEJKOVA, E ;
HINZE, H ;
LEUSCHEL, L ;
WEBER, H ;
BECKSPEIER, I .
FEBS LETTERS, 1989, 250 (02) :221-226
[39]   Nitric oxide donor drugs [J].
Megson, IL .
DRUGS OF THE FUTURE, 2000, 25 (07) :701-715
[40]  
Mei JM, 2000, CANCER RES, V60, P3379