Eicosanoids and renal vascular function in diseases

被引:68
作者
Imig, John D. [1 ]
机构
[1] Med Coll Georgia, Dept Physiol, Vasc Biol Ctr, Augusta, GA 30912 USA
关键词
cyclo-oxygenase (COX); cytochrome P450 (CYP450); epoxyeicosatrienoic acid (EET); hypertension; kidney; metabolic syndrome; obesity;
D O I
10.1042/cs20050251
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Arachidonic acid metabolites are vital for the proper control of renal haemodynamics and, when not properly controlled, can contribute to renal vascular injury and end-stage renal disease. Three major enzymatic pathways, COX (cyclo-oxygenase), CYP450 (cytochrome P450) and LOX (lipoxygenase), are responsible for the metabolism of arachidonic acid metabolites to bioactive eicosanoids. These eicosanoids can dilate or constrict the renal vasculature and maintain vascular resistance in the face of changing vasoactive hormones. Renal vascular generation of eicosanoids is altered in pathophysiological conditions such as hypertension, diabetes, metabolic syndrome and acute renal failure. Experimental evidence supports the concept that altered eicosanoid metabolism contributes to renal haemodynamic alterations and the development and progression of nephropathy. The possible beneficial renal vascular actions of enzymatic inhibitors, eicosanoid analogues and receptor antagonists have been examined in hypertension, diabetes and metabolic syndrome. This review highlights the roles of renal vascular eicosanoids in the pathogenesis of nephropathy and therapeutic targets for renal disease related to hypertension, diabetes, metabolic syndrome and acute renal failure.
引用
收藏
页码:21 / 34
页数:14
相关论文
共 159 条
  • [71] INCREASED RENAL TXA2 SYNTHESIS IN DIABETES-MELLITUS - SIMULTANEOUS DETERMINATION OF URINARY TXB2 AND 2,3-DINOR-TXB2
    KATAYAMA, S
    INABA, M
    MARUNO, Y
    OMOTO, A
    KAWAZU, S
    ISHII, J
    SAWADA, M
    [J]. PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS, 1990, 39 (01): : 47 - 51
  • [72] RENAL HEMODYNAMIC ACTIONS OF LIPOXINS IN RATS - A COMPARATIVE PHYSIOLOGICAL STUDY
    KATOH, T
    TAKAHASHI, K
    DEBOER, DK
    SERHAN, CN
    BADR, KF
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 263 (03): : F436 - F442
  • [73] TP receptors regulate renal hemodynamics during angiotensin II slow pressor response
    Kawada, N
    Dennehy, K
    Solis, G
    Modlinger, P
    Hamel, R
    Kawada, JT
    Aslam, S
    Moriyama, T
    Imai, E
    Welch, WJ
    Wilcox, CS
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2004, 287 (04) : F753 - F759
  • [74] Lipoxins: Potential anti-inflammatory, proresolution, and antifibrotic mediators in renal disease
    Kieran, NE
    Maderna, P
    Godson, C
    [J]. KIDNEY INTERNATIONAL, 2004, 65 (04) : 1145 - 1154
  • [75] Design, synthesis, and biological activity of 1,3-Disubstituted ureas as potent inhibitors of the soluble epoxide hydrolase of increased water solubility
    Kim, IH
    Morisseau, C
    Watanabe, T
    Hammock, BD
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 2004, 47 (08) : 2110 - 2122
  • [76] Kirschenbaum M A, 1986, Contrib Nephrol, V50, P36
  • [77] KIRSCHENBAUM MA, 1986, MINER ELECTROL METAB, V12, P352
  • [78] Treatment of hypertension in diabetic patients with nephropathy.
    Komers R.
    Anderson S.
    [J]. Current Diabetes Reports, 2001, 1 (3) : 251 - 260
  • [79] Renal and cardiovascular effects of selective cyclooxygenase-2 inhibitors
    Komers, R
    Anderson, S
    Epstein, M
    [J]. AMERICAN JOURNAL OF KIDNEY DISEASES, 2001, 38 (06) : 1145 - 1157
  • [80] Localization of cyclooxygenase-1 and -2 in adult and fetal human kidney: Implication for renal function
    Komhoff, M
    Grone, HJ
    Klein, T
    Seyberth, HW
    Nusing, RM
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 1997, 272 (04) : F460 - F468