Large-conductance calcium-activated potassium channels modulate vascular tone in experimental cirrhosis
Article first published online: 12 MAR 2008
© 2008 The Authors. Journal compilation © 2008 Blackwell Munksgaard
Volume 28, Issue 4, pages 566–573, April 2008
How to Cite
Rodríguez-Vilarrupla, A., Graupera, M., Matei, V., Bataller, R., Abraldes, J. G., Bosch, J. and García-Pagán, J.-C. (2008), Large-conductance calcium-activated potassium channels modulate vascular tone in experimental cirrhosis. Liver International, 28: 566–573. doi: 10.1111/j.1478-3231.2008.01668.x
- Issue published online: 12 MAR 2008
- Article first published online: 12 MAR 2008
- Received 12 July 2007Accepted 22 November 2007
- BKCa expression;
- nitric oxide;
- perfused livers;
- portal pressure;
- real-time PCR
Background: Large-conductance calcium-activated potassium (BKCa) channels regulate vascular tone in different vascular systems. Moreover, activated hepatic stellate cells (HSC) contain BKCa channels. The aim of this study was to evaluate the role of BKCa channels in the regulation of vascular tone in control (CT) and carbon tetrachloride-cirrhotic (CH) rat livers.
Methods: Changes in intrahepatic vascular resistance were assessed by evaluating the portal perfusion pressure (PP) response to methoxamine (Mtx) in the presence of Iberiotoxin (Ibtx; a BKCa channel blocker), NS1619 (a BKCa channel opener), Ibtx plus the nitric oxide (NO) synthase inhibitor, NG-nitro-l-arginine (l-NNA) or l-NNA alone. In addition, in CH livers, PP dose–response curves to the NO donor, S-nitroso-N-acetyl-d,l-penicillamine (SNAP), were performed after pre-incubation with Ibtx or its vehicle. BKCa mRNA expression was assessed in liver homogenates, and BKCa protein expression in HSC isolated from CT and CH livers.
Results: In CH livers, Ibtx significantly increased baseline PP and exacerbated the PP response to Mtx. Conversely, NS1619 induced a mild nonsignificant decrease of baseline PP and attenuated the hyperresponse to Mtx. CH livers exhibited an upregulation of both mRNA and protein of the α-subunit of BKCa.
Conclusion: Large-conductance calcium-activated potassium channels are overexpressed in CH livers and might represent a compensatory mechanism modulating the increased hepatic vascular tone of cirrhosis.