8,9-Epoxyeicosatrienoic acid protects the glomerular filtration barrier

被引:36
|
作者
Sharma, Mukut [1 ]
McCarthy, Ellen T. [2 ]
Reddy, D. Sudarshan [3 ]
Patel, Paresh K. [3 ]
Savin, Virginia J. [1 ]
Medhora, Meetha [4 ]
Falck, John R. [3 ]
机构
[1] Med Coll Wisconsin, Div Nephrol, Dept Med, Milwaukee, WI 53226 USA
[2] Univ Kansas, Med Ctr, Kidney Inst, Kansas City, KS 66103 USA
[3] Univ Texas SW Med Ctr Dallas, Dept Biochem, Dallas, TX 75390 USA
[4] Med Coll Wisconsin, Div Pulm & Crit Care, Dept Med, Milwaukee, WI 53226 USA
关键词
Epoxyeicosatrienoic acids; 8,9-EET; Glomerular filtration barrier; FSGS; Albumin permeability; Chronic kidney disease; FOCAL SEGMENTAL GLOMERULOSCLEROSIS; ISOLATED RAT GLOMERULI; INCREASES ALBUMIN PERMEABILITY; EPOXYEICOSATRIENOIC ACIDS; ARACHIDONIC-ACID; ENDOTHELIAL-CELLS; 11,12-EPOXYEICOSATRIENOIC ACID; EPOXYGENASE METABOLITES; MESANGIAL CELLS; UP-REGULATION;
D O I
10.1016/j.prostaglandins.2009.04.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Glomerular dysfunction and proteinuria characterize focal segmental glomerulosclerosis (FSGS) associated with chronic kidney disease. FSGS is resistant to treatment and a Circulating permeability factor (FSPF) frequently causes post-renal transplantation recurrence. In order to explore the role of 5,6-, 8,9-, 11,12- and 14,15-epoxyeicosatrienoic acids (EETs), we determined their effect on FSPF-induced increase in glomerular albumin permeability (P-alb) Using an in vitro assay. Exogenous 8,9-EET (1-1000 nM) dose-dependently prevented the FSPF-induced increase in P-alb. The other three EET regioisomers, 8,9-EET metabolite, 8,9-dihydroxyeicosatrienoic acid and unrelated 11,14-eicosadienoic acid (100 nM each) were not effective suggesting specificity of the observed glomerular protection by 8,9-EET. Synthetic analogs of 8,9-EET containing one double bond antagonized the effect of 8,9-EET on the FSPF-induced increase in P-alb. Analogs containing two double bonds did not antagonize the effect of 8,9-EET and significantly blocked the FSPF-induced increase in P-alb. These novel findings suggest a unique protective role for 8,9-EET in the glomerulus. Stable analogs of 8,9-EET may be valuable in developing effective management/treatment of glomerular dysfunction. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:43 / 51
页数:9
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