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Am J Physiol Renal Physiol 278: F702-F707, 2000;
0363-6127/00 $5.00
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Vol. 278, Issue 5, F702-F707, May 2000

Localization of protein inhibitor of neuronal nitric oxide synthase in rat kidney

Agnes Roczniak2, David Z. Levine1,2, and Kevin D. Burns1,2

Departments of 1 Medicine and 2 Cellular and Molecular Medicine, University of Ottawa and Ottawa Hospital, Ottawa, Ontario, Canada K1H 8L6

We have recently demonstrated that in rats with 5/6 nephrectomy (5/6 Nx), renal cortical and inner medullary neuronal NOS (nNOS) expression is downregulated, associated with decreased urinary excretion of nitric oxide (NO) products. Recently, a novel 89-amino acid protein [protein inhibitor of nNOS (PIN)] was isolated from rat brain and shown to inhibit nNOS activity. The present studies localized PIN in the rat kidney and determined the effect of 5/6 Nx on PIN expression. By RT-PCR, PIN mRNA was detected in the kidney cortex and inner medulla. Immunohistochemistry revealed staining for PIN in glomerular and vasa rectae endothelial cells. PIN was also localized to the apical membranes of inner medullary collecting duct (IMCD) cells. Two weeks after 5/6 Nx, inner medullary PIN expression was significantly upregulated (sham, 0.18 ± 0.07 vs. 5/6 Nx, 0.58 ± 0.13 arbitrary units; n = 6, P < 0.02), as determined by Western blotting. In summary, our data show that PIN, a specific inhibitor of nNOS activity, is expressed in the IMCD, a site of high nNOS expression in the kidney. PIN expression is upregulated in the inner medulla of 5/6 Nx rats. Inhibition of nNOS activity by PIN may have important implications for the regulation of NO synthesis in the IMCD of normal and remnant kidneys.

inner medulla; chronic renal failure


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