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Journal of the American Society of Nephrology, Vol 3, 1710-1716, Copyright © 1993 by American Society of Nephrology
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S Orisio, N Perico, L Benatti, L Longaretti, S Amuchastegui and G Remuzzi
Mario Negri Institute for Pharmacological Research Bergamo, Italy.
Experimental evidence is available to indicate that intrarenal mechanisms play a role in the impaired salt excretion of nephrotic syndrome by multiple and still incompletely defined mediators. It is documented herein that the gene encoding for cyclophilin-like protein (Cy-LP) is up-regulated in renal medulla from adriamycin (ADR)-treated rats as compared with control animals. In the cortex of rats with ADR nephrosis, no change in Cy-LP as compared with that in controls was found for the entire observation period. By contrast, in the medulla of nephrotic rats, Cy-LP gene expression was significantly higher than in controls. Values of urinary Na excretion were inversely correlated to Cy-LP mRNA expression levels. Because in ADR nephrosis a blunted natriuretic response to ANP has been previously reported, it was investigated whether ANP infusion modulated Cy-LP mRNA in the renal medulla. ADR-treated rats, but not control rats, infused for 1 h with ANP (1 microgram/kg.min) had a significant (P < 0.05) increase in medullary Cy-LP mRNA as compared with nephrotic animals receiving the vehicle alone. These findings might be taken to suggest that renal Cy- LP gene expression is positively modulated in nephrotic syndrome and parallels changes in sodium excretion.
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G. DESCHENES and A. DOUCET Collecting Duct Na+/K+-ATPase Activity Is Correlated with Urinary Sodium Excretion in Rat Nephrotic Syndromes J. Am. Soc. Nephrol., April 1, 2000; 11(4): 604 - 615. [Abstract] [Full Text] [PDF] |
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Copyright © 2008 by the American Society of Nephrology. Online ISSN: 1533-3450 Print ISSN: 1046-6673