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Am J Physiol Renal Physiol 295: F1044-F1051, 2008. First published July 30, 2008; doi:10.1152/ajprenal.90278.2008
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Radicicol, a heat shock protein 90 inhibitor, reduces glomerular filtration rate

Victoria Ramírez, Juan M. Mejía-Vilet, Damián Hernández, Gerardo Gamba, and Norma A. Bobadilla

Molecular Physiology Unit, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México and Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico

Submitted 29 April 2008 ; accepted in final form 24 July 2008

The heat shock protein subfamily of 90 kDa (HSP90) is composed of five isoforms. The more abundant proteins of this subfamily are cytosolic isoforms known as HSP90{alpha} and HSP90β. More than 100 client proteins have been found to be regulated by HSP90. Several studies have shown that HSP90 regulates nitric oxide synthesis that is dependent on endothelial nitric oxide synthase (eNOS). Because eNOS regulates renal vascular tone and glomerular filtration rate (GFR), the present study was designed to evaluate the effect of acute HSP90 inhibition with radicicol on GFR and the eNOS pathway. Twenty male Wistar rats were divided into two groups: control vehicle animals and radicicol-infused animals (25 µg·ml–1·min–1). Basal levels were taken before experimental measurements. Mean arterial pressure and renal blood flow (RBF) were recorded, as well as GFR, urinary nitrite and nitrate excretion (UNO2/NO3V). Additionally, we evaluated eNOS expression, Ser1177 and Thr495 eNOS phosphorylation levels, the eNOS dimer-to-monomer ratio, as well as oxidative stress by assessing renal lipoperoxidation and urinary isoprostane F2{alpha} and hydrogen peroxide. HSP90 inhibition with radicicol produced a fall in RBF and GFR that was associated with a significant reduction of UNO2/NO3V. The effects of radicicol were in part mediated by a significant decrease in eNOS phosphorylation and in the eNOS dimer-to-monomer ratio. Our findings suggest that GFR is in part maintained by HSP90-eNOS interaction.

renal blood flow; heat shock protein 90 isoforms



Address for reprint requests and other correspondence: N. A. Bobadilla, Unidad de Fisiología Molecular, Vasco de Quiroga No. 15, Tlalpan, 14000 Mexico City, Mexico (e-mail: nab{at}biomedicas.unam.mx, nabs{at}quetzal.innsz.mx)







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