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Radicicol Inhibits iNOS Expression in Cytokine-Stimulated Pancreatic Beta Cells. | LitMetric

Radicicol Inhibits iNOS Expression in Cytokine-Stimulated Pancreatic Beta Cells.

Korean J Physiol Pharmacol

DNA Damage Response Network Center, Chosun University, Kwangju 501-709, Korea. ; Department of Pharmacology, School of Medicine, Chosun University, Gwangju 501-759, Korea.

Published: August 2013

Here, we show that radicicol, a fungal antibiotic, resulted in marked inhibition of inducible nitric oxide synthase (iNOS) transcription by the pancreatic beta cell line MIN6N8a in response to cytokine mixture (CM: TNF-α, IFN-γ, and IL-1β). Treatment of MIN6N8a cells with radicicol inhibited CM-stimulated activation of NF-κB/Rel, which plays a critical role in iNOS transcription, in a dose-related manner. Nitrite production in the presence of PD98059, a specific inhibitor of the extracellular signal-regulated protein kinase-1 and 2 (ERK1/2) pathway, was dramatically diminished, suggesting that the ERK1/2 pathway is involved in CM-induced iNOS expression. In contrast, SB203580, a specific inhibitor of p38, had no effect on nitrite generation. Collectively, this series of experiments indicates that radicicol inhibits iNOS gene expression by blocking ERK1/2 signaling. Due to the critical role that NO release plays in mediating destruction of pancreatic beta cells, the inhibitory effects of radicicol on iNOS expression suggest that radicicol may represent a useful anti-diabetic activity.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3741488PMC
http://dx.doi.org/10.4196/kjpp.2013.17.4.315DOI Listing

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