Tadalafil for the Treatment of Lower Urinary Tract Symptoms Secondary to Benign Prostatic Hyperplasia: Pathophysiology and Mechanism(s) of Action

被引:183
作者
Andersson, Karl-Erik [1 ]
de Groat, William C. [2 ,3 ]
McVary, Kevin T. [4 ]
Lue, Tom F. [5 ]
Maggi, Mario [6 ]
Roehrborn, Claus G. [7 ]
Wyndaele, Jean Jacques [8 ,9 ]
Melby, Thomas [10 ]
Viktrup, Lars [11 ]
机构
[1] Wake Forest Univ, Bowman Gray Sch Med, Wake Forest Inst Regenerat Med, Winston Salem, NC 27157 USA
[2] Univ Pittsburgh, Sch Med, Dept Pharmacol, Pittsburgh, PA 15261 USA
[3] Univ Pittsburgh, Sch Med, Dept Biol Chem, Pittsburgh, PA USA
[4] Northwestern Univ, Feinberg Sch Med, Dept Urol, Chicago, IL 60611 USA
[5] Univ Calif San Francisco, Dept Urol, San Francisco, CA 94143 USA
[6] Univ Florence, Dept Clin Physiopathol, Androl Unit, Florence, Italy
[7] UT SW Med Ctr Dallas, Dallas, TX USA
[8] Univ Antwerp, Dept Urol, Edegem, Belgium
[9] Univ Antwerp Hosp, UZA, Edegem, Belgium
[10] i3 Statprobe, Med Writing, Minneapolis, MN USA
[11] Eli Lilly & Co, Lilly Res Lab, Indianapolis, IN 46285 USA
关键词
PDE5; phosphodiesterases; prostatic hyperplasia; urinary tract; NERVE GROWTH-FACTOR; PHOSPHODIESTERASE PDE ISOENZYMES; BLADDER OUTLET OBSTRUCTION; CYCLIC-NUCLEOTIDE LEVELS; NITRIC-OXIDE PATHWAY; SMOOTH-MUSCLE TONE; CHRONIC ISCHEMIA; ERECTILE DYSFUNCTION; SEXUAL DYSFUNCTION; RISK-FACTORS;
D O I
10.1002/nau.20999
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
The PDE5 inhibitor tadalafil is under investigation for the treatment of lower urinary tract symptoms (LUTS) in men with benign prostatic hyperplasia (BPH). Several clinical studies of tadalafil and other PDE5 inhibitors have reported significant symptom reduction but limited urinary flow rate improvement. This manuscript reviews the published literature describing the pathophysiology of male LUTS, with an emphasis on mechanisms that may be modulated or improved by phosphodiesterase type 5 (PDE5) inhibition. Methods: Literature (through March 2010) was obtained via Medline searches and from the individual reviewers files. Articles were selected for review based on describing in vitro, preclinical, or clinical studies of pathological processes contributing to LUTS, or possible effects of PDE5 inhibition in the lower urinary tract. Results: Major mechanisms contributing to LUTS include: reduced nitric oxide/cyclic guanosine monophosphate signaling; increased RhoA kinase pathway activity; autonomic overactivity; increased bladder afferent activity; and pelvic ischemia. Tadalafil and other PDE5 inhibitors have demonstrated beneficial effects on smooth muscle relaxation, smooth muscle and endothelial cell proliferation, nerve activity, and tissue perfusion that may impact LUTS in men. Conclusions: The pathophysiology of male LUTS is complex and not completely understood. LUTS may occur independently of BPH or secondary to BPH but in both cases involve obstructive or irritative mechanisms with substantial pathophysiological overlap. While the precise mechanism remains unclear, inhibition of PDE5 seems to have an effect on several pathways that may impact LUTS. Neurourol. Urodynam. 30:292-301, 2011. (C) 2011 Wiley-Liss, Inc.
引用
收藏
页码:292 / 301
页数:10
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