Specialized Pro-resolving Lipid Mediators: Modulation of Diabetes-Associated Cardio-, Reno-, and Retino-Vascular Complications

被引:27
作者
de Gaetano, Monica [1 ,2 ]
McEvoy, Caitriona [1 ,2 ,3 ]
Andrews, Darrell [1 ,2 ]
Cacace, Antonino [1 ,2 ]
Hunter, Jonathan [1 ,2 ]
Brennan, Eoin [1 ,2 ]
Godson, Catherine [1 ,2 ]
机构
[1] Univ Coll Dublin, Conway Inst, UCD Diabet Complicat Res Ctr, Dublin, Ireland
[2] Univ Coll Dublin, UCD Sch Med, Dublin, Ireland
[3] Univ Hlth Network, Renal Transplant Program, Toronto, ON, Canada
基金
爱尔兰科学基金会;
关键词
diabetic kidney disease; diabetes-associated atherosclerosis; diabetic retinopathy; lipoxins; resolvins; REVERSE CHOLESTEROL TRANSPORT; ASPIRIN-TRIGGERED LIPOXIN; GLYCATION END-PRODUCTS; SMOOTH-MUSCLE-CELLS; MACULAR EDEMA; GROWTH-FACTOR; APOPTOTIC NEUTROPHILS; INSULIN-RESISTANCE; NLRP3; INFLAMMASOME; 15(R/S)-METHYL-LIPOXIN A(4);
D O I
10.3389/fphar.2018.01488
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Diabetes and its associated chronic complications present a healthcare challenge on a global scale. Despite improvements in the management of chronic complications of the micro-/macro-vasculature, their growing prevalence and incidence highlights the scale of the problem. It is currently estimated that diabetes affects 425 million people globally and it is anticipated that this figure will rise by 2025 to 700 million people. The vascular complications of diabetes including diabetes-associated atherosclerosis and kidney disease present a particular challenge. Diabetes is the leading cause of end stage renal disease, reflecting fibrosis leading to organ failure. Moreover, diabetes associated states of inflammation, neo-vascularization, apoptosis and hypercoagulability contribute to also exacerbate atherosclerosis, from the metabolic syndrome to advanced disease, plaque rupture and coronary thrombosis. Current therapeutic interventions focus on regulating blood glucose, glomerular and peripheral hypertension and can at best slow the progression of diabetes complications. Recently advanced knowledge of the pathogenesis underlying diabetes and associated complications revealed common mechanisms, including the inflammatory response, insulin resistance and hyperglycemia. The major role that inflammation plays in many chronic diseases has led to the development of new strategies aiming to promote the restoration of homeostasis through the "resolution of inflammation." These strategies aim to mimic the spontaneous activities of the 'specialized pro-resolving mediators' (SPMs), including endogenous molecules and their synthetic mimetics. This review aims to discuss the effect of SPMs [with particular attention to lipoxins (LXs) and resolvins (Rvs)] on inflammatory responses in a series of experimental models, as well as evidence from human studies, in the context of cardio- and renovascular diabetic complications, with a brief mention to diabetic retinopathy (DR). These data collectively support the hypothesis that endogenously generated SPMs or synthetic mimetics of their activities may represent lead molecules in a new discipline, namely the 'resolution pharmacology,' offering hope for new therapeutic strategies to prevent and treat, specifically, diabetes-associated atherosclerosis, nephropathy and retinopathy.
引用
收藏
页数:23
相关论文
共 282 条
[1]   Atheroprone Flow Activation of the Sterol Regulatory Element Binding Protein 2 and Nod-Like Receptor Protein 3 Inflammasome Mediates Focal Atherosclerosis [J].
Abe, Jun-ichi ;
Berk, Bradford C. .
CIRCULATION, 2013, 128 (06) :579-582
[2]   Chronic diseases 1 - The burden and costs of chronic diseases in low-income and middle-income countries [J].
Abegunde, Dele O. ;
Mathers, Colin D. ;
Adam, Taghreed ;
Ortegon, Monica ;
Strong, Kathleen .
LANCET, 2007, 370 (9603) :1929-1938
[3]   The genetics of diabetic complications [J].
Ahlqvist, Emma ;
van Zuydam, Natalie R. ;
Groop, Leif C. ;
McCarthy, Mark I. .
NATURE REVIEWS NEPHROLOGY, 2015, 11 (05) :277-287
[4]   Bone morphogenetic proteins and their antagonists: current and emerging clinical uses [J].
Ali, Imran H. A. ;
Brazil, Derek P. .
BRITISH JOURNAL OF PHARMACOLOGY, 2014, 171 (15) :3620-3632
[5]   Contribution of Intimal Smooth Muscle Cells to Cholesterol Accumulation and Macrophage-Like Cells in Human Atherosclerosis [J].
Allahverdian, Sima ;
Chehroudi, Ali Cyrus ;
McManus, Bruce M. ;
Abraham, Thomas ;
Francis, Gordon A. .
CIRCULATION, 2014, 129 (15) :1551-1559
[6]   Antiplatelet Therapy in Diabetes: Efficacy and Limitations of Current Treatment Strategies and Future Directions [J].
Angiolillo, Dominick J. .
DIABETES CARE, 2009, 32 (04) :531-540
[7]   Resolvin E1 selectively interacts with leukotriene B4 receptor BLT1 and ChemR23 to regulate inflammation [J].
Arita, Makoto ;
Ohira, Taisuke ;
Sun, Yee-Ping ;
Elangovan, Siva ;
Chiang, Nan ;
Serhan, Charles N. .
JOURNAL OF IMMUNOLOGY, 2007, 178 (06) :3912-3917
[8]   Metabolic inactivation of resolvin E1 and stabilization of its anti-inflammatory actions [J].
Arita, Makoto ;
Oh, Sungwhan F. ;
Chonan, Tomomichi ;
Hong, Song ;
Elangovan, Siva ;
Sun, Yee-Ping ;
Uddin, Jasim ;
Petasis, Nicos A. ;
Serhan, Charles N. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (32) :22847-22854
[9]   The human heart contains distinct macrophage subsets with divergent origins and functions [J].
Bajpai, Geetika ;
Schneider, Caralin ;
Wong, Nicole ;
Bredemeyer, Andrea ;
Hulsmans, Maarten ;
Nahrendorf, Matthias ;
Epelman, Slava ;
Kreisel, Daniel ;
Liu, Yongjian ;
Itoh, Akinobu ;
Shankar, Thirupura S. ;
Selzman, Craig H. ;
Drakos, Stavros G. ;
Lavine, Kory J. .
NATURE MEDICINE, 2018, 24 (08) :1234-+
[10]   Lipoxin A4: Anti-Inflammatory and Anti-Angiogenic Impact on Endothelial Cells [J].
Baker, Nicole ;
O'Meara, Sarah J. ;
Scannell, Michael ;
Maderna, Paola ;
Godson, Catherine .
JOURNAL OF IMMUNOLOGY, 2009, 182 (06) :3819-3826