Targeting cytosolic phospholipase A2 by arachidonyl trifluoromethyl ketone prevents chronic inflammation in mice

被引:25
作者
Malaviya, Ravi
Ansell, Justin
Hall, LeRoy
Fahmy, Mila
Argentieri, Rochelle L.
Olini, Gilbert C., Jr.
Pereira, David W.
Sur, Runa
Cavender, Druie
机构
[1] Johnson & Johnson Pharmaceut Res & Dev LLC, Dept Drug Discovery, Inflammat Res Team, Raritan, NJ 08869 USA
[2] Johnson & Johnson Pharmaceut Res & Dev LLC, Dept Drug Evaluat, Raritan, NJ 08869 USA
关键词
inflammation; acute; chronic; inhibitor; phospholipase A(2);
D O I
10.1016/j.ejphar.2006.03.018
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cytosolic phospholipase A(2) (cPLA(2)) plays a pivotal role in inflammation by catalyzing the release of arachidonic acid, a substrate for lipoxygenase and cyclooxygenase enzymes, from membrane phospholipids. In the present study we examined the role of cPLA2 in inflammatory responses through the use of a specific inhibitor of the enzyme, cPLA2, arachidonyl trifluoromethyl ketone (AACOCF3). Interestingly, we observed that AACOCF3 is an inhibitor of chronic but not acute inflammatory responses. Specifically, AACOCF3 inhibited phorbol 12-myristate 13-acetate (PMA)-induced chronic ear edema in mice. Additionally, oral treatment of ovalbumin-sensitized/ovalbumin-challenged BALB/c mice with 20mg/kg AACOCF3 prevented the development of airway hyper-responsiveness in a model of asthma. Furthermore, AACOCF3 decreased cellular recruitment in the airway lumen and airway inflammation after the ovalbumin challenge. Taken together, these results suggest that a potent and specific chemical inhibitor of cPLA2 may be useful for the treatment of chronic inflammatory diseases including rheumatoid arthritis, inflammatory bowel disease, psoriasis, and asthma. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:195 / 204
页数:10
相关论文
共 66 条
[1]   INHIBITION OF MACROPHAGE CA2+-INDEPENDENT PHOSPHOLIPASE A(2) BY BROMOENOL LACTONE AND TRIFLUOROMETHYL KETONES [J].
ACKERMANN, EJ ;
CONDEFRIEBOES, K ;
DENNIS, EA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (01) :445-450
[2]  
[Anonymous], 1991, SINO W CULTURAL RELA, V13, P4
[3]   THE PATHOBIOLOGY OF BRONCHIAL-ASTHMA [J].
ARM, JP ;
LEE, TH .
ADVANCES IN IMMUNOLOGY, 1992, 51 :323-382
[4]   Regulation and inhibition of phospholipase A2 [J].
Balsinde, J ;
Balboa, MA ;
Insel, PA ;
Dennis, EA .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 1999, 39 :175-189
[5]  
BARTOLI F, 1994, J BIOL CHEM, V269, P15625
[6]  
Bonventre JV, 1999, J AM SOC NEPHROL, V10, P404
[7]  
Bonventre JV, 2002, ADV EXP MED BIOL, V507, P25
[8]  
Börsch-Haubold AG, 1998, BIOCHEM SOC T, V26, P350
[9]  
Burke JR, 2001, J PHARMACOL EXP THER, V298, P376
[10]   Nuclear factor kB is activated by arachidonic acid but not by eicosapentaenoic acid [J].
Camandola, S ;
Leonarduzzi, G ;
Musso, T ;
Varesio, L ;
Carini, R ;
Scavazza, A ;
Chiarpotto, E ;
Baeuerle, PA ;
Poli, G .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 229 (02) :643-647