Lipid inflammatory mediators in diabetic vascular disease

被引:180
作者
Natarajan, R
Nadler, JL
机构
[1] City Hope Natl Med Ctr, Beckman Res Inst, Gonda Diabet Res Ctr, Duarte, CA 91010 USA
[2] Univ Virginia, Sch Med, Diabet & Hormone Ctr Excellence, Charlottesville, VA 22908 USA
关键词
lipoxygenase; diabetes; diabetes complications; inflammation; lipids;
D O I
10.1161/01.ATV.0000133606.69732.4c
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Type 2 diabetes is associated with significantly accelerated rates of macrovascular complications such as atherosclerosis. Emerging evidence now indicates that atherosclerosis is an inflammatory disease and that certain inflammatory markers may be key predictors of diabetic atherosclerosis. Proinflammatory cytokines and cellular adhesion molecules expressed by vascular and blood cells during stimulation by growth factors and cytokines seem to play major roles in the pathophysiology of atherosclerosis and diabetic vascular complications. However, more recently, data suggest that inflammatory responses can also be elicited by smaller oxidized lipids that are components of atherogenic oxidized low-density lipoprotein or products of phospholipase activation and arachidonic acid metabolism. These include oxidized lipids of the lipoxygenase and cyclooxygenase pathways of arachidonic acid and linoleic acid metabolism. These lipids have potent growth, vasoactive, chemotactic, oxidative, and proinflammatory properties in vascular smooth muscle cells, endothelial cells, and monocytes. Cellular and animal models indicate that these enzymes are induced under diabetic conditions, have proatherogenic effects, and also mediate the actions of growth factors and cytokines. This review highlights the roles of the inflammatory cyclooxygenase and 12/15-lipoxygenase pathways in the pathogenesis of diabetic vascular disease.
引用
收藏
页码:1542 / 1548
页数:7
相关论文
共 98 条
[1]   A natural protective mechanism against hyperglycaemia in vascular endothelial and smooth-muscle cells: role of glucose and 12-hydroxyeicosatetraenoic acid [J].
Alpert, E ;
Gruzman, A ;
Totary, H ;
Kaiser, N ;
Reich, R ;
Sasson, S .
BIOCHEMICAL JOURNAL, 2002, 362 (02) :413-422
[2]   A 12-lipoxygenase product, 12-hydroxyeicosatetraenoic acid, is increased in diabetics with incipient and early renal disease [J].
Antonipillai, I ;
Nadler, J ;
Vu, EJ ;
Bughi, S ;
Natarajan, R ;
Horton, R .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1996, 81 (05) :1940-1945
[3]   Diabetes and atherosclerosis - Epidemiology, pathophysiology, and management [J].
Beckman, JA ;
Creager, MA ;
Libby, P .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2002, 287 (19) :2570-2581
[4]   Resistance to type 1 diabetes induction in 12-lipoxygenase knockout mice [J].
Bleich, D ;
Chen, SY ;
Zipser, B ;
Sun, DX ;
Funk, CD ;
Nadler, JL .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (10) :1431-1436
[5]   ELEVATED GLUCOSE ALTERS EICOSANOID RELEASE FROM PORCINE AORTIC ENDOTHELIAL-CELLS [J].
BROWN, ML ;
JAKUBOWSKI, JA ;
LEVENTIS, LL ;
DEYKIN, D .
JOURNAL OF CLINICAL INVESTIGATION, 1988, 82 (06) :2136-2141
[6]   Biochemistry and molecular cell biology of diabetic complications [J].
Brownlee, M .
NATURE, 2001, 414 (6865) :813-820
[7]  
BROWNLEE M, 1988, NEW ENGL J MED, V318, P1315
[8]   Cyclooxygenase-2 promotes early atherosclerotic lesion formation in LDL receptor-deficient mice [J].
Burleigh, ME ;
Babaev, VR ;
Oates, JA ;
Harris, RC ;
Gautam, S ;
Riendeau, D ;
Marnett, LJ ;
Morrow, JD ;
Fazio, S ;
Linton, MF .
CIRCULATION, 2002, 105 (15) :1816-1823
[9]  
CHEN XS, 1994, J BIOL CHEM, V269, P13979
[10]   The receptor RAGE as a progression factor amplifying arachidonate-dependent inflammatory and proteolytic response in human atherosclerotic plaques - Role of glycemic control [J].
Cipollone, F ;
Iezzi, A ;
Fazia, M ;
Zucchelli, M ;
Pini, B ;
Cuccurullo, C ;
De Cesare, D ;
De Blasis, G ;
Muraro, R ;
Bei, R ;
Chiarelli, F ;
Schmidt, AM ;
Cuccurullo, F ;
Mezzetti, A .
CIRCULATION, 2003, 108 (09) :1070-1077