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XB-ART-48053
Am J Physiol Renal Physiol. October 1, 2013; 305 (7): F995-F1005.

Fulvene-5 inhibition of Nadph oxidases attenuates activation of epithelial sodium channels in A6 distal nephron cells.

Trac D , Liu B , Pao AC , Thomas SV , Park M , Downs CA , Ma HP , Helms MN .


Abstract
Nadph oxidase 4 is an important cellular source of reactive oxygen species (ROS) generation in the kidney. Novel antioxidant drugs, such as Nox4 inhibitor compounds, are being developed. There is, however, very little experimental evidence for the biological role and regulation of Nadph oxidase isoforms in the kidney. Herein, we show that Fulvene-5 is an effective inhibitor of Nox-generated ROS and report the role of Nox isoforms in activating epithelial sodium channels (ENaC) in A6 distal nephron cells via oxidant signaling and cell stretch activation. Using single-channel patch-clamp analysis, we report that Fulvene-5 blocked the increase in ENaC activity that is typically observed with H2O2 treatment of A6 cells: average ENaC NPo values decreased from a baseline level of 1.04 ± 0.18 (means ± SE) to 0.25 ± 0.08 following Fulvene-5 treatment. H2O2 treatment failed to increase ENaC activity in the presence of Fulvene-5. Moreover, Fulvene-5 treatment of A6 cells blocked the osmotic cell stretch response of A6 cells, indicating that stretch activation of Nox-derived ROS plays an important role in ENaC regulation. Together, these findings indicate that Fulvene-5, and perhaps other classes of antioxidant inhibitors, may represent a novel class of compounds useful for the treatment of pathological disorders stemming from inappropriate ion channel activity, such as hypertension.

PubMed ID: 23863470
PMC ID: PMC3798745
Article link: Am J Physiol Renal Physiol.
Grant support: R00-HL09222601 NHLBI NIH HHS , R00-HL09222601 NHLBI NIH HHS , R00-HL09222601 NHLBI NIH HHS , R00-HL09222601 NHLBI NIH HHS , R00-HL09222601 NHLBI NIH HHS , R00-HL09222601 NHLBI NIH HHS , R01-DK067110 NIDDK NIH HHS , T32 DK007357 NIDDK NIH HHS

Genes referenced: nox4
Antibodies referenced:

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