Bumetanide and other high-ceiling diuretics (HCD) attenuate myogenic tone and contractions of vascular smooth muscle cells (VSMC) triggered by diverse stimuli. HCD outcome may be mediated by their interaction with NKCC1, the only isoform of Na+, K+, 2Cl(-) cotransporter expressed in VSMC as well as with targets distinct from this carrier. To examine these hypotheses, we compared the effect of bumetanide on contractions of mesenteric arteries from wild-type and NKCC1 knockout mice. in mesenteric arteries from wild-type controls, 100 mu M bumetanide evoked a decrease of up to 4-fold in myogenic tone and contractions triggered by modest [K+](o)-induced depolarization, phenylephrine and UTP. These actions of bumetanide were preserved after inhibition of nitric oxide synthase with NG-nitro-L-arginine methyl show that bumetanide inhibits ester, but were absent in mesenteric arteries from NKCC1(-1-) mice. The data VSMC contractile responses via its interaction with NKCC1 and independently of nitric oxide production by endothelial cells. (C) 2009 Elsevier Inc. All rights reserved.