Fibrosis and Loss of Smooth Muscle in the Corpora Cavernosa Precede Corporal Veno-Occlusive Dysfunction (CVOD) Induced by Experimental Cavernosal Nerve Damage in the Rat

被引:95
作者
Ferrini, Monica G. [1 ,2 ]
Kovanecz, Istvan [2 ,3 ]
Sanchez, Sandra [3 ]
Umeh, Chiome [3 ]
Rajfer, Jacob [2 ,3 ]
Gonzalez-Cadavid, Nestor F. [1 ,2 ,3 ]
机构
[1] Charles R Drew Univ Med & Sci, Dept Med, Los Angeles, CA 90059 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Dept Urol, Los Angeles, CA 90095 USA
[3] Harbor UCLA Med Ctr, Los Angeles Biomed Res Inst, Div Urol, Torrance, CA 90509 USA
基金
美国国家卫生研究院;
关键词
Fibrosis; Erectile Dysfunction; Smooth Muscle; Nerve Sparing; Radical Prostatectomy; Penis; Nitric Oxide; cGMP; Collagen; Inducible Nitric Oxide Synthase; Apoptosis; NITRIC-OXIDE SYNTHASE; RADICAL RETROPUBIC PROSTATECTOMY; PEYRONIES FIBROTIC PLAQUE; ERECTILE DYSFUNCTION; POSTRADICAL PROSTATECTOMY; GENE-THERAPY; PREVENTS; CARDIOPROTECTION; DIFFERENTIATION; MYOSTATIN;
D O I
10.1111/j.1743-6109.2008.01105.x
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
Corporal veno-occlusive dysfunction (CVOD), which usually is associated with a loss of smooth muscle cells (SMC) and an increase in fibrosis within the corpora cavernosa, can be induced by an injury to the cavernosal nerves. The corporal tissue expresses inducible nitric oxide synthase (iNOS), presumably as an antifibrotic and SMC-protective response. We studied the temporal relationship in the corpora between the expression of iNOS, other histological and biochemical changes, and the development of CVOD, after bilateral cavernosal nerve resection (BCNR) in the rat. Rats underwent either BCNR or sham operation. Cavernosometry was performed 1, 3, 7, 15, 30, and 45 days (N = 8/groups) after surgery. Penile tissue sections were subjected to Masson trichrome staining for SMC and collagen, and immunodetection for alpha smooth muscle actin, iNOS, neuronal NOS (nNOS), endothelial NOS (eNOS), proliferating cell nuclear antigen (PCNA), and terminal transferase dUTP nick end labeling (TUNEL). Quantitative western blot analysis was done in homogenates. Time course on the development of fibrosis and CVOD. Following BCNR, CVOD was detectable 30 days later, and it became more pronounced by 45 days. In contrast, the SMC/collagen ratio in the BCNR corpora was reduced at 7 days and bottomed at 30 and 45 days, due in part to the reduction of SMC, presumably caused by an increase in apoptosis peaking at 3 days. PCNA also peaked at 3 days, but then decayed. nNOS was reduced early (3-7 days) and disappeared at 30 days, whereas eNOS was not affected. iNOS was induced at day 3, and steadily increased peaking at 30 days. CVOD develops in the BCNR rat as a result of the early loss of corporal SMC by the neuropraxia-induced apoptosis, which the initial cell replication response cannot counteract, followed by fibrosis. The time course of iNOS induction supports the antifibrotic role of iNOS. Ferrini MG, Kovanecz I, Sanchez S, Umeh C, Rajfer J, and Gonzalez-Cadavid NF. Fibrosis and loss of smooth muscle in the corpora cavernosa precede corporal veno-occlusive dysfunction (CVOD) induced by experimental cavernosal nerve damage in the rat. J Sex Med 2009;6:415-428.
引用
收藏
页码:415 / 428
页数:14
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