Department of Urology, Wake Forest University Baptist Medical Center, Winston-Salem, North Carolina.
Wake Forest Institute for Regenerative Medicine, Wake Forest Baptist Medical Center, Winston-Salem, North Carolina.
Neurourol Urodyn. 2018 Sep;37(7):2141-2150. doi: 10.1002/nau.23536. Epub 2018 Aug 31.
Persistent urinary incontinence (UI) and/or erectile dysfunction (ED) occur in 30-50% of post-radical prostatectomy patients regardless of nerve sparing approaches. Identification of potential treatment options for these patients will require testing in an animal model that develops these chronic conditions. The objective was to characterize a nonhuman primate (NHP) model of persistent post-prostatectomy ED and UI and then test the feasibility of periurethral injection of the chemokine CXCL-12.
Ten adult male cynomolgus monkeys were used. Two were used for study of normal male nonhuman primate genitourinary anatomy. Five were used for measures of sexual behavior, peak intra-corporal pressure (ICP), abdominal leak point pressures (ALPP) 3 and 6-months post open radical prostatectomy (ORP). Three additional ORP animals received ultrasound-guided peri-urethral injection of chemokine CXCL12 6 weeks after ORP, and UI/ED evaluated for up to 3 months.
The anatomy, innervation, and vascular supply to the prostate and surrounding tissues of these male NHPs are substantially similar to those of human beings. ORP resulted in complete removal of the prostate gland along with both neurovascular bundles and seminal vesicles while permitting stable restoration of vesico-urethral patency. ORP produced sustained (6 months) decreases in ALPP, ICP's, and sexual function. Transurethral injection of chemokine CXCL12 was feasible and had beneficial effects on erectile and urinary function.
ORP in NHPs produced persistent erectile and urinary tract dysfunction. Periurethral injection of CXCL-12 was feasible and improved both urinary incontinence and erectile dysfunction and suggests that this model can be used to test new approaches for both conditions.
无论是否采用神经保留方法,根治性前列腺切除术后 30-50%的患者会出现持续性尿失禁(UI)和/或勃起功能障碍(ED)。需要在一种会发展为这些慢性疾病的动物模型中测试这些患者的潜在治疗选择。本研究的目的是建立一种非人类灵长类动物(NHP)模型,以研究根治性前列腺切除术后持续性 ED 和 UI,并测试趋化因子 CXCL-12 经尿道周围注射的可行性。
使用 10 只成年雄性食蟹猴。其中 2 只为研究正常雄性非人类灵长类动物的泌尿生殖解剖结构而使用。5 只为研究性行为、峰值阴茎体内压(ICP)、术后 3 个月和 6 个月的腹压漏点压(ALPP)而使用。另外 3 只接受经超声引导的前列腺切除术后 6 周行趋化因子 CXCL12 经尿道周围注射,最长随访 3 个月,以评估 UI/ED。
这些雄性 NHP 的前列腺及其周围组织的解剖结构、神经支配和血管供应与人类非常相似。前列腺切除术(ORP)导致前列腺、神经血管束和精囊完全切除,但允许稳定恢复膀胱尿道通畅性。ORP 导致 ALPP、ICP 和性功能持续(6 个月)下降。趋化因子 CXCL12 经尿道注射是可行的,对勃起和尿功能有有益的影响。
ORP 可导致 NHP 出现持续性勃起和尿路功能障碍。趋化因子 CXCL-12 经尿道周围注射是可行的,可改善尿失禁和勃起功能障碍,并提示该模型可用于测试这两种疾病的新方法。