Article ID Journal Published Year Pages File Type
6168119 Urology 2011 6 Pages PDF
Abstract
Imatinib induced prostatic smooth muscle relaxation in vitro. This effect was suppressed by l-NAME and ODQ, showing a dependence on the nitric oxide-cyclic guanosine monophosphate pathway and modulated by the KATP and BKCa2+ K+ channels. Our findings suggest that imatinib can augment relaxation of human prostatic tissues by way of a novel ligand-protein tyrosine kinase signaling pathway.
Related Topics
Health Sciences Medicine and Dentistry Nephrology
Authors
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