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本文引用的文献

1
Stem-cell therapy for erectile dysfunction.用于勃起功能障碍的干细胞疗法。
Biomed Mater Eng. 2017;28(s1):S81-S85. doi: 10.3233/BME-171627.
2
Stem cell therapies in post-prostatectomy erectile dysfunction: a critical review.前列腺切除术后勃起功能障碍的干细胞疗法:一项批判性综述。
Can J Urol. 2017 Feb;24(1):8609-8619.
3
Erectile dysfunction post-radical prostatectomy - a challenge for both patient and physician.根治性前列腺切除术后勃起功能障碍——对患者和医生而言都是一项挑战。
J Med Life. 2017 Jan-Mar;10(1):13-18.
4
Cancer Statistics, 2017.《2017 年癌症统计》
CA Cancer J Clin. 2017 Jan;67(1):7-30. doi: 10.3322/caac.21387. Epub 2017 Jan 5.
5
Local versus intravenous injections of skeletal muscle precursor cells in nonhuman primates with acute or chronic intrinsic urinary sphincter deficiency.在患有急性或慢性固有尿道括约肌功能不全的非人灵长类动物中,局部注射与静脉注射骨骼肌前体细胞的比较。
Stem Cell Res Ther. 2016 Oct 7;7(1):147. doi: 10.1186/s13287-016-0411-3.
6
Role of stromal cell-derived factor 1α pathway in bone metastatic prostate cancer.基质细胞衍生因子1α通路在前列腺癌骨转移中的作用
J Biomed Res. 2016 May;30(3):181-5. doi: 10.7555/JBR.30.20150114. Epub 2015 Nov 2.
7
Cell versus Chemokine Therapy in a Nonhuman Primate Model of Chronic Intrinsic Urinary Sphincter Deficiency.细胞与趋化因子治疗在慢性内在性尿道括约肌缺陷的非人灵长类动物模型中。
J Urol. 2016 Dec;196(6):1809-1815. doi: 10.1016/j.juro.2016.05.106. Epub 2016 Jun 4.
8
Posterior musculofascial reconstruction after radical prostatectomy: an updated systematic review and a meta-analysis.前列腺癌根治术后的后肌筋膜重建:一项更新的系统评价和荟萃分析。
BJU Int. 2016 Jul;118(1):20-34. doi: 10.1111/bju.13480. Epub 2016 Apr 7.
9
Combination Therapy Using Human Adipose-derived Stem Cells on the Cavernous Nerve and Low-energy Shockwaves on the Corpus Cavernosum in a Rat Model of Post-prostatectomy Erectile Dysfunction.在前列腺切除术后勃起功能障碍大鼠模型中,采用人脂肪源性干细胞联合海绵体神经治疗及低能量冲击波联合海绵体治疗
Urology. 2016 Feb;88:226.e1-9. doi: 10.1016/j.urology.2015.10.021. Epub 2015 Oct 29.
10
Delivery of human mesenchymal adipose-derived stem cells restores multiple urological dysfunctions in a rat model mimicking radical prostatectomy damages through tissue-specific paracrine mechanisms.在模拟根治性前列腺切除术损伤的大鼠模型中,通过组织特异性旁分泌机制递送人间充质脂肪来源干细胞可恢复多种泌尿系统功能障碍。
Stem Cells. 2016 Feb;34(2):392-404. doi: 10.1002/stem.2226. Epub 2015 Oct 23.

非人类灵长类动物前列腺根治术后持续性勃起和排尿功能障碍模型:微创治疗的可行性。

Nonhuman primate model of persistent erectile and urinary dysfunction following radical prostatectomy: Feasibility of minimally invasive therapy.

机构信息

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.

出版信息

Neurourol Urodyn. 2018 Sep;37(7):2141-2150. doi: 10.1002/nau.23536. Epub 2018 Aug 31.

DOI:10.1002/nau.23536
PMID:30168617
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8261895/
Abstract

OBJECTIVE

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.

METHODS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

目的

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。

方法

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。

结果

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。

结论

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。