Calpain inhibitor I reduces the development of acute and chronic inflammation

被引:62
作者
Cuzzocrea, S
McDonald, MC
Mazzon, E
Siriwardena, D
Serraino, I
Dugo, L
Britti, D
Mazzullo, G
Caputi, AP
Thiemermann, C
机构
[1] Univ Messina, Inst Pharmacol, Messina, Italy
[2] St Bartholomews & Royal London Sch Med, William Harvey Res Inst, London, England
[3] Univ Messina, Sch Med, Dept Biomorphol, Messina, Italy
[4] Univ Messina, Dept Vet Med & Pharmacol, Messina, Italy
[5] Univ Messina, Inst Vet Gen Pathol & Pathol Anat, Messina, Italy
关键词
D O I
10.1016/S0002-9440(10)64845-6
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
There is limited evidence that inhibition of the activity of the protease calpain I reduces inflammation. Here we investigate the effects of calpain inhibitor I in animal models of acute and chronic inflammation (carrageenan-induced pleurisy and collagen-induced arthritis). We report here for the first time that calpain inhibitor I (given at 5, 10, or 20 mg/kg i.p. in the pleurisy model or at 5 mg/kg i.p every 48 hours in the arthritis model) exerts potent anti-inflammatory effects (eg, inhibition of pleural exudate formation, mononuclear cell infiltration, delayed the development of the clinical signs and histological injury) in vivo. Furthermore, calpain inhibitor I reduced (1) the staining for nitrotyrosine and poly (ADP-ribose) polymerase (immunohistochemistry) and (2) the expression of inducible nitric oxide synthase and cyclooxygenase-2 in the lungs of carrageenan-treated rats and in joints from collagen-treated rats. Thus, prevention of the activation of calpain I reduces the development of acute and chronic inflammation. Inhibition of calpain I activity may represent a novel therapeutic approach for the therapy of inflammation.
引用
收藏
页码:2065 / 2079
页数:15
相关论文
共 71 条
[1]   STRUCTURE OF THE HUMAN CYCLO-OXYGENASE-2 GENE [J].
APPLEBY, SB ;
RISTIMAKI, A ;
NEILSON, K ;
NARKO, K ;
HLA, T .
BIOCHEMICAL JOURNAL, 1994, 302 :723-727
[2]   ROLE OF CALCIUM-ACTIVATED NEUTRAL PROTEASE (CALPAIN) IN CELL-DEATH IN CULTURED NEONATAL RAT CARDIOMYOCYTES DURING METABOLIC INHIBITION [J].
ATSMA, DE ;
BASTIAANSE, EML ;
JERZEWSKI, A ;
VANDERVALK, LJM ;
VANDERLAARSE, A .
CIRCULATION RESEARCH, 1995, 76 (06) :1071-1078
[3]   ACTIVATION OF DNA-BINDING ACTIVITY IN AN APPARENTLY CYTOPLASMIC PRECURSOR OF THE NF-KAPPA-B TRANSCRIPTION FACTOR [J].
BAEUERLE, PA ;
BALTIMORE, D .
CELL, 1988, 53 (02) :211-217
[4]   Mechanisms of disease - Nuclear factor-kappa b - A pivotal transcription factor in chronic inflammatory diseases [J].
Barnes, PJ ;
Larin, M .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 336 (15) :1066-1071
[5]   CALPAIN AS A NOVEL TARGET FOR TREATING ACUTE NEURODEGENERATIVE DISORDERS [J].
BARTUS, RT ;
ELLIOTT, PJ ;
HAYWARD, NJ ;
DEAN, RL ;
HARBESON, S ;
STRAUB, JA ;
LI, Z ;
POWERS, JC .
NEUROLOGICAL RESEARCH, 1995, 17 (04) :249-258
[6]  
BAUERLE PA, 1994, ANNU REV IMMUNOL, V12, P141
[7]   APPARENT HYDROXYL RADICAL PRODUCTION BY PEROXYNITRITE - IMPLICATIONS FOR ENDOTHELIAL INJURY FROM NITRIC-OXIDE AND SUPEROXIDE [J].
BECKMAN, JS ;
BECKMAN, TW ;
CHEN, J ;
MARSHALL, PA ;
FREEMAN, BA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (04) :1620-1624
[8]   Oxidative damage and tyrosine nitration from peroxynitrite [J].
Beckman, JS .
CHEMICAL RESEARCH IN TOXICOLOGY, 1996, 9 (05) :836-844
[9]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[10]   MUTUAL REGULATION OF THE TRANSCRIPTIONAL ACTIVATOR NF-KAPPA-B AND ITS INHIBITOR, I-KAPPA-B-ALPHA [J].
BROWN, K ;
PARK, S ;
KANNO, T ;
FRANZOSO, G ;
SIEBENLIST, U .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (06) :2532-2536