Curbing Inflammation through Endogenous Pathways: Focus on Melanocortin Peptides

被引:34
作者
Ahmed, Tazeen J. [1 ]
Montero-Melendez, Trinidad [1 ]
Perretti, Mauro [1 ]
Pitzalis, Costantino [1 ,2 ]
机构
[1] Barts andThe London Sch Med, William Harvey Res Inst, Charterhouse Sq, London EC1M 6BQ, England
[2] Barts & London Queen Marys Sch Med & Dent, Ctr Expt Med & Rheumatol, John Vane Sci Ctr, William Harvey Res Inst, London EC1M 6BQ, England
基金
英国惠康基金;
关键词
D O I
10.1155/2013/985815
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The resolution of inflammation is now known to be an active process, armed with a multitude of mediators both lipid and protein in nature. Melanocortins are peptides endowed with considerable promise with their proresolution and anti-inflammatory effects in preclinical models of inflammatory disease, with tissue protective effects. These peptides and their targets are appealing because they can be seen as a natural way of inducing these effects as they harness endogenous pathways of control. Whereas most of the information generated about these mediators derives from several acute models of inflammation (such as zymosan induced peritonitis), there is some indication that these mediatorsmay inhibit chronic inflammation by modulating cytokines, chemokines, and leukocyte apoptosis. In addition, proresolving mediators and their mimics have often been tested alongside therapeutic protocols, hence have been tested in settings more relevant to real life clinical scenarios. We provide here an overview on some of these mediators with a focus on melanocortin peptides and receptors, proposing that they may unveil new opportunities for innovative treatments of inflammatory arthritis.
引用
收藏
页数:10
相关论文
共 80 条
[1]   Targeting cytokines to inflammation sites [J].
Adams, G ;
Vessillier, S ;
Dreja, H ;
Chernajovsky, Y .
NATURE BIOTECHNOLOGY, 2003, 21 (11) :1314-1320
[2]   IDENTIFICATION OF ANTAGONISTS FOR MELANOCORTIN MC(3), MC(4) AND MC(5) RECEPTORS [J].
ADAN, RAH ;
OOSTEROM, J ;
LUDVIGSDOTTIR, G ;
BRAKKEE, JH ;
BURBACH, JPH ;
GISPEN, WH .
EUROPEAN JOURNAL OF PHARMACOLOGY-MOLECULAR PHARMACOLOGY SECTION, 1994, 269 (03) :331-337
[3]   Molecular circuits of resolution: Formation and actions of resolvins and protectins [J].
Bannenberg, GL ;
Chiang, N ;
Ariel, A ;
Arita, M ;
Tjonahen, E ;
Gotlinger, KH ;
Hong, S ;
Serhan, CN .
JOURNAL OF IMMUNOLOGY, 2005, 174 (07) :4345-4355
[4]  
Bellingan GJ, 1996, J IMMUNOL, V157, P2577
[5]   Treatment of Acute Relapses in Multiple Sclerosis [J].
Berkovich, Regina .
NEUROTHERAPEUTICS, 2013, 10 (01) :97-105
[6]  
Bhardwaj RS, 1996, J IMMUNOL, V156, P2517
[7]   Characterization of cell lines stably expressing human normal or mutated EGFP-tagged MC4R [J].
Blondet, A ;
Doghman, M ;
Rached, M ;
Durand, P ;
Bégeot, M ;
Naville, D .
JOURNAL OF BIOCHEMISTRY, 2004, 135 (04) :541-546
[8]   Role of Proopiomelanocortin-Derived Peptides and Their Receptors in the Osteoarticular System: From Basic to Translational Research [J].
Boehm, Markus ;
Graessel, Susanne .
ENDOCRINE REVIEWS, 2012, 33 (04) :623-651
[9]   Detection of functionally active melanocortin receptors and evidence for an immunoregulatory activity of α-melanocyte-stimulating hormone in human dermal papilla cells [J].
Böhm, MB ;
Eickelmann, M ;
Li, Z ;
Schneider, SW ;
Oji, V ;
Diederichs, S ;
Barsh, GS ;
Vogt, A ;
Stieler, K ;
Blume-Peytavi, U ;
Luger, TA .
ENDOCRINOLOGY, 2005, 146 (11) :4635-4646
[10]   α-melanocyte-stimulating hormone and related tripeptides:: Biochemistry, antiinflammatory and protective effects in vitro and in vivo, and future perspectives for the treatment of immune-mediated inflammatory diseases [J].
Brzoska, Thomas ;
Luger, Thomas A. ;
Maaser, Christian ;
Abels, Christoph ;
Boehm, Markus .
ENDOCRINE REVIEWS, 2008, 29 (05) :581-602