Endothelin-1 and nitric oxide in the pathogenesis of urinary tract disorders secondary to bladder outlet obstruction
- PMID: 15320850
- DOI: 10.2174/1570161033386600
Endothelin-1 and nitric oxide in the pathogenesis of urinary tract disorders secondary to bladder outlet obstruction
Abstract
Bladder outlet obstruction (BOO) is a common disorder that is associated with urinary tract symptoms. Nitric oxide (NO), synthesized by NO synthase (NOS) is a potent vasodilator that is present throughout the urinary tract and the corpus cavernosum. Endothelin-1 (ET-1) conversely is a potent vasoconstrictor peptide that is similarly distributed throughout the urinary tract. ET-1 and NO as well as possessing opposing actions regulate each other's synthesis. The disruption of the balance between ET-1 and NO is associated with various vascular pathologies. However, their potential roles in the pathogenesis of urinary tract disorders, secondary to BOO, is not well established. New Zealand White rabbits with BOO are considered to be a suitable model of the human condition. Hence, using this model, we systematically investigated the potential roles of ET-1 and NO in the pathogenesis of the various urological disorders associated with BOO. In this review we discuss the results of our studies, which support the concept that an imbalance between ET-1 and NO may be associated with the pathogenesis of urinary tract disorders secondary to BOO. We also discuss the potential clinical implications of this association. This review is based on the Bard Silver Medal Lecture given (by MAK) at the 2002 British Association of Urological Surgeons (BAUS) annual meeting.
Similar articles
-
Up-regulation of endothelin (ET(A) and ET(B)) receptors and down-regulation of nitric oxide synthase in the detrusor of a rabbit model of partial bladder outlet obstruction.Urol Res. 1999 Dec;27(6):445-53. doi: 10.1007/s002400050134. Urol Res. 1999. PMID: 10651133
-
Endothelin-1 and urinary bladder hyperplasia following partial bladder outlet obstruction.J Cardiovasc Pharmacol. 2000 Nov;36(5 Suppl 1):S262-3. doi: 10.1097/00005344-200036051-00077. J Cardiovasc Pharmacol. 2000. PMID: 11078393
-
Possible role of endothelin-1 in the rabbit urinary bladder hyperplasia secondary to partial bladder outlet obstruction.Scand J Urol Nephrol. 2000 Feb;34(1):15-20. doi: 10.1080/003655900750016823. Scand J Urol Nephrol. 2000. PMID: 10757264
-
MicroRNAs in Bladder Outlet Obstruction: Relationship to Growth and Matrix Remodelling.Basic Clin Pharmacol Toxicol. 2016 Oct;119 Suppl 3:5-17. doi: 10.1111/bcpt.12534. Epub 2016 Jan 14. Basic Clin Pharmacol Toxicol. 2016. PMID: 26612603 Review.
-
Drug treatments for lower urinary tract symptoms secondary to bladder outflow obstruction: focus on quality of life.Drugs. 2003;63(18):1947-62. doi: 10.2165/00003495-200363180-00004. Drugs. 2003. PMID: 12930164 Review.
Cited by
-
Update on Phosphodiesterase Type 5 Inhibitors for the Treatment of Lower Urinary Tract Symptoms due to Benign Prostatic Hyperplasia.Rev Urol. 2012;14(3-4):79-86. Rev Urol. 2012. PMID: 23526698 Free PMC article.
-
Excitability and contractility in arterioles and venules from the urinary bladder.Curr Top Membr. 2020;85:301-326. doi: 10.1016/bs.ctm.2020.01.003. Epub 2020 Feb 17. Curr Top Membr. 2020. PMID: 32402643 Free PMC article. Review.
-
Effect of ethanol on the response of the rat urinary bladder to in vitro ischemia: protective effect of alpha-lipoic acid.Mol Cell Biochem. 2005 Mar;271(1-2):133-8. doi: 10.1007/s11010-005-5870-2. Mol Cell Biochem. 2005. PMID: 15881664
-
Inhibition of vascular smooth muscle inward-rectifier K+ channels restores myogenic tone in mouse urinary bladder arterioles.Am J Physiol Renal Physiol. 2017 May 1;312(5):F836-F847. doi: 10.1152/ajprenal.00682.2016. Epub 2017 Feb 1. Am J Physiol Renal Physiol. 2017. PMID: 28148533 Free PMC article.
-
Phosphodiesterase type 5 inhibitors for the treatment of male lower urinary tract symptoms.Rev Urol. 2007 Spring;9(2):73-7. Rev Urol. 2007. PMID: 17592540 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources