Role of epoxyeicosatrienoic acids in renal functional response to inhibition of NO production in the rat

G. O. Ogungbade, L. A. Akinsanmi, H. Jiang, A. O. Oyekan
2003 AJP - Renal Physiology  
tric oxide (NO) inhibits hemoproteins, including cytochrome (CYP) 2C, the gene responsible for the production of epoxyeicosatrienoic acids (EETs). EETs and NO are produced in the kidney, and both regulate renal vascular tone and Na ϩ transport. However, the role of EETs in NO-mediated renal function is not known. This study tested the hypothesis that NO tonically regulates the renal production of EETs, thereby impacting renal vasomotor tone and electrolyte balance. LPS (10 mg/kg iv) inhibited
more » ... /kg iv) inhibited microsomal conversion of 14 C-labeled arachidonic acid to EETs and reduced mean arterial blood pressure (MABP; ⌬ ϭ 63 Ϯ 5 mmHg). Nitro-L-arginine methyl ester (L-NAME, 10 mg/kg), an inhibitor of NO synthase, increased MABP (⌬ ϭ 26 Ϯ 6 mmHg), reduced cortical (CBF) and medullary (MBF) blood flow (⌬ ϭ Ϫ0.86 Ϯ 0.15 and Ϫ0.34 Ϯ 0.09 V, respectively) and glomerular filtration rate (GFR; from 0.82 Ϯ 0.16 to 0.32 Ϯ 0.10 ml ⅐ g kidney Ϫ1 ⅐ min Ϫ1 ), and increased Na ϩ excretion (UNaV, from 0.16 Ϯ 0.04 to 0.30 Ϯ 0.06 mol ⅐ g kidney Ϫ1 ⅐ min Ϫ1 ). 2-(2-Propynyloxy)-benzenehexanoic acid (PPOH), a suicide substrate inhibitor of EET production, did not affect the L-NAME-induced increase in MABP but attenuated the effects of L-NAME on CBF (31 Ϯ 7%, P Ͻ 0.05%), GFR (44 Ϯ 6%, P Ͻ 0.05), and UNaV (78 Ϯ 7%, P Ͻ 0.05). Miconazole (1.3 mg ⅐ kg Ϫ1 ⅐ h Ϫ1 ), a heme inhibitor of epoxygenase enzymes, produced effects similar to those of PPOH. Renal intraarterial infusion of 5, 6-, 8,9-, 11,12-, and 14,15-EET (1-10 ng/min) elicited dose-dependent reductions in CBF and GFR accompanied by regioisomeric changes in MBF, UNaV, and urine flow rate. In addition, 11,12-EET dose dependently restored the PPOH blunting the effects of L-NAME on CBF, MBF, and GFR. We conclude that NO tonically regulates epoxygenase activity and that EETs are renal vaosoconstrictors in vivo and contribute, at least in part, to the renal functional responses following inhibition of NO production. cytochrome P-450; kidney NITRIC OXIDE (NO) is an important endogenous regulator of renal vascular tone and ion transport and, therefore, has a number of effects that have an impact on the regulation of renal function and blood pressure (3). It Address for reprint requests and other correspondence: A. O.
doi:10.1152/ajprenal.00092.2003 pmid:12865253 fatcat:rglgxacoofdrdkr7njictuvwsq