A Comparative Study of the Efficacy of Intralesional Verapamil Versus Normal Saline Injection in a Novel Peyronie Disease Animal Model: Assessment of Immunohistopathological Changes and Erectile Function Outcome

被引:31
作者
Chung, Eric [1 ,3 ]
Garcia, Francisco [1 ]
De Young, Ling [2 ]
Solomon, Matthew [1 ,3 ]
Brock, Gerald B. [2 ]
机构
[1] St Joseph Hlth Care, Div Urol, London, ON, Canada
[2] Lawson Hlth Res Inst, Dept Urol, London, ON, Canada
[3] Princess Alexandra Hosp, Dept Urol, Brisbane, Qld 4102, Australia
关键词
penis; penile induration; penile erection; verapamil; smooth muscle actin; rat; FIBROTIC PLAQUE; SINGLE-BLIND; MATRIX; RAT; DIFFERENTIATION; PROLIFERATION; SAFETY;
D O I
10.1016/j.juro.2012.08.191
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
Purpose: While intralesional injections improve penile curvature and decrease plaque volume, the exact mechanism of action on Peyronie disease is unknown. We evaluated penile curvature, immunohistology and erectile function outcomes after intralesional injections of verapamil and normal saline in a previously described Peyronie disease animal model. Materials and Methods: Peyronie plaque was induced in 12 adult male rats using an established Peyronie disease animal model. At 4 weeks the rats were divided into group 1-5 with 0.1 mg/0.1 ml intralesional verapamil injected every second day for 2 weeks, group 2-5 with 0.1 ml intralesional normal saline injection and group 3-2 that served as controls. At weeks 6 and 8 penile pressure was measured and serial immunohistochemical staining of penile tissue sections was done. Results: Intralesional injection of verapamil and normal saline resulted in macroscopic and microscopic changes to penile curvature and Peyronie plaque size. Decreased collagen and elastin fibers were measured with a significant reduction in smooth muscle alpha-actin (p < 0.05). Changes were greater in group 1 than group 2 (p < 0.05). Intralesional verapamil injection was associated with greater recovery of electrostimulated penile pressure, a surrogate of erectile function, than in the saline and control groups. Conclusions: To our knowledge this novel study offers for the first time histological evidence of cellular changes and improvement in penile pressure studies in rats with Peyronie plaque after intralesional verapamil injection therapy in a Peyronie disease animal model.
引用
收藏
页码:380 / 384
页数:5
相关论文
共 23 条
[1]  
Alenghat Francis J, 2002, Sci STKE, V2002, ppe6, DOI 10.1126/stke.2002.119.pe6
[2]   Inhibition of Peyronie's plaque fibroblast proliferation by biologic agents [J].
Anderson, MS ;
Shankey, TV ;
Lubrano, T ;
Mulhall, JP .
INTERNATIONAL JOURNAL OF IMPOTENCE RESEARCH, 2000, 12 (Suppl 3) :S25-S31
[3]   Intralesional verapamil prevents the progression of Peyronie's disease [J].
Bennett, Nelson E. ;
Guhring, Patricia ;
Mulhall, John P. .
UROLOGY, 2007, 69 (06) :1181-1184
[4]   Open preliminary randomized prospective clinical trial of efficacy and safety of three different verapamil dilutions for intraplaque therapy of Peyronie's disease [J].
Cavallini, Giorgio ;
Modenini, Fablo ;
Vital, Giovanni .
UROLOGY, 2007, 69 (05) :950-954
[5]   Rat as an animal model for Peyronie's disease research: a review of current methods and the peer-reviewed literature [J].
Chung, E. ;
De Young, L. ;
Brock, G. B. .
INTERNATIONAL JOURNAL OF IMPOTENCE RESEARCH, 2011, 23 (06) :235-241
[6]  
El-Sakka AI, 1998, BRIT J UROL, V81, P445
[7]  
Garcia F, 2012, CAN UROL ASS J S, V6, pS51
[8]   Single-blind, multicenter, placebo controlled, parallel study to assess the safety and efficacy of intralesional interferon α-2b for minimally invasive treatment for Peyronie's disease [J].
Hellstrom, Wayne J. G. ;
Kendirci, Muammer ;
Matern, Richard ;
Cockerham, Yolanda ;
Myers, Leann ;
Sikka, Suresh C. ;
Venable, Dennis ;
Honig, Stanton ;
McCullough, Andrew ;
Hakim, Lawrence S. ;
Nehra, Ajay ;
Templeton, Lance E. ;
Pryor, Jon L. .
JOURNAL OF UROLOGY, 2006, 176 (01) :394-398
[9]  
KOHN EC, 1994, J BIOL CHEM, V269, P21505
[10]   CALCIUM-ANTAGONISTS RETARD EXTRACELLULAR-MATRIX PRODUCTION IN CONNECTIVE-TISSUE EQUIVALENT [J].
LEE, RC ;
PING, J .
JOURNAL OF SURGICAL RESEARCH, 1990, 49 (05) :463-466