20-hydroxyeicosatetraenoic acid, endothelial dysfunction and hypertension

被引:0
作者
Kunert, Mary Pat [1 ]
Drenjancevic, Ines [2 ]
机构
[1] Univ Wisconsin, Coll Nursing, Milwaukee, WI 53211 USA
[2] Univ Josip Juraj Strossmayer, Fac Med Osijek, Osijek, Croatia
关键词
20-HETE; hypertension; endothelial dysfunction; VASCULAR SMOOTH-MUSCLE; ENDOTOXIN-INDUCED HYPOTENSION; ACTIVATED PROTEIN-KINASE; CYTOCHROME-P-450; OMEGA-HYDROXYLASE; HIGH-SALT DIET; ARACHIDONIC-ACID; NITRIC-OXIDE; ANGIOTENSIN-II; OXIDATIVE STRESS; BLOOD-PRESSURE;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
20-hydroxyeicosatrienoic acid (20-HETE) is a metabolite of arachidonic acid formed by the enzymatic activity of cytochrome P450 omega hydroxylases of the 4A and 4F isoform families (CYP 450 4A and 4F). The role of the metabolites of arachidonic acid (AA) formed by cyclooxygenases and lipoxygenases in mediating cardiovascular function have been studied and known for a long time. More recently, particularly in the last 10-15 years, the importance of the role that the CYP450 omega hydroxylase/20-HETE system plays in cardiovascular, inflammatory and neoplastic diseases, has captured the attention of the scientific community. In this brief review we discuss some of the more recent findings related to the function of 20-HETE in the cardiovascular system. In particular we focus on the interactions of 20-HETE with the intracellular pathways of nitric oxide and the renin angiotensin system and discuss how it plays a role in oxidative stress, the development of endothelial dysfunction and experimental and human hypertension. To date the research strongly suggests that 20-HETE is an important and central mediator of cardiovascular function, and that alterations in the normal regulation of the CYP450/20-HETE system play a role in the pathogenesis of many disorders. There is great potential for the development of therapeutic agents to modify the activation and activity of this system in order to prevent and/or treat hypertension.
引用
收藏
页码:170 / 180
页数:11
相关论文
共 145 条
[1]   Contribution of 20-HETE to vasodilator actions of nitric oxide in the cerebral microcirculation [J].
Alonso-Galicia, M ;
Hudetz, AG ;
Shen, H ;
Harder, DR ;
Roman, RJ .
STROKE, 1999, 30 (12) :2727-2734
[2]   20-HETE agonists and antagonists in the renal circulation [J].
Alonso-Galicia, M ;
Falck, JR ;
Reddy, KM ;
Roman, RJ .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 1999, 277 (05) :F790-F796
[3]   Role of 20-hydroxyeicosatetraenoic acid in the renal and vasoconstrictor actions of angiotensin II [J].
Alonso-Galicia, M ;
Maier, KG ;
Greene, AS ;
Cowley, AW ;
Roman, RJ .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2002, 283 (01) :R60-R68
[4]   Contribution of 20-HETE to the vasodilator actions of nitric oxide in renal arteries [J].
Alonso-Galicia, M ;
Sun, CW ;
Falck, JR ;
Harder, DR ;
Roman, RJ .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 1998, 275 (03) :F370-F378
[5]   Inhibition of 20-HETE production contributes to the vascular responses to nitric oxide [J].
AlonsoGalicia, M ;
Drummond, HA ;
Reddy, KK ;
Falck, JR ;
Roman, RJ .
HYPERTENSION, 1997, 29 (01) :320-325
[6]   Alteration of cardiac cytochrome P450-mediated arachidonic acid metabolism in response to lipopolysaccharide-induced acute systemic inflammation [J].
Anwar-mohamed, Anwar ;
Zordoky, Beshay N. M. ;
Aboutabl, Mona E. ;
El-Kadi, Ayman O. S. .
PHARMACOLOGICAL RESEARCH, 2010, 61 (05) :410-418
[7]   Inhibition of Ca2+/calmodulin-dependent protein kinase II, RAS-GTPase and 20-hydroxyeicosatetraenoic acid attenuates the development of diabetes-induced vascular dysfunction in the rat carotid artery [J].
Benter, IF ;
Yousif, MHM ;
Canatan, H ;
Akhtar, S .
PHARMACOLOGICAL RESEARCH, 2005, 52 (03) :252-257
[8]   Ovariectomy, but not estrogen deficiency, increases CYP4A modulation of α1-adrenergic vasoconstriction in aging female rats [J].
Berezan, Dellice J. ;
John, Yi ;
Falck, John R. ;
Kundu, Asish P. ;
Davidge, Sandra T. .
AMERICAN JOURNAL OF HYPERTENSION, 2008, 21 (06) :685-690
[9]   Human pulmonary arteries dilate to 20-HETE, an endogenous eicosanoid of lung tissue [J].
Birks, EK ;
Bousamra, M ;
Presberg, K ;
Marsh, JA ;
Effros, RM ;
Jacobs, ER .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1997, 272 (05) :L823-L829
[10]   Nitric oxide/cytochrome P450 interactions in cyclosporin A-induced effects in the rat [J].
Blanton, Ahmad ;
Nsaif, Rami ;
Hercule, Hantz ;
Oyekan, Adebayo .
JOURNAL OF HYPERTENSION, 2006, 24 (09) :1865-1872