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本文引用的文献

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Cytokine expression after vaginal distention of different durations in virgin Sprague-Dawley rats.处女Sprague-Dawley大鼠不同时长阴道扩张后的细胞因子表达
J Urol. 2008 Aug;180(2):753-9. doi: 10.1016/j.juro.2008.03.182. Epub 2008 Jun 13.
2
Development of a device to standardize leak point pressure experiments in rats.一种用于标准化大鼠漏点压力实验的装置的研发。
Neurourol Urodyn. 2008;27(6):553-8. doi: 10.1002/nau.20591.
3
Muscle derived stem cell therapy for stress urinary incontinence.肌肉来源干细胞治疗压力性尿失禁。
World J Urol. 2008 Aug;26(4):327-32. doi: 10.1007/s00345-008-0269-9. Epub 2008 May 10.
4
Adult stem cell therapy of female stress urinary incontinence.成年干细胞疗法治疗女性压力性尿失禁。
Eur Urol. 2008 Jan;53(1):169-75. doi: 10.1016/j.eururo.2007.07.026. Epub 2007 Jul 23.
5
Autologous myoblasts and fibroblasts versus collagen for treatment of stress urinary incontinence in women: a randomised controlled trial.自体成肌细胞与成纤维细胞对比胶原蛋白治疗女性压力性尿失禁:一项随机对照试验。
Lancet. 2007 Jun 30;369(9580):2179-2186. doi: 10.1016/S0140-6736(07)61014-9.
6
Striated muscle and nerve fascicle distribution in the female rat urethral sphincter.雌性大鼠尿道括约肌中的横纹肌和神经束分布。
Anat Rec (Hoboken). 2007 Feb;290(2):145-54. doi: 10.1002/ar.20420.
7
Over expression of stem cell homing cytokines in urogenital organs following vaginal distention.阴道扩张后泌尿生殖器官中干细胞归巢细胞因子的过表达
J Urol. 2007 Apr;177(4):1568-72. doi: 10.1016/j.juro.2006.11.047.
8
Increased duration of simulated childbirth injuries results in increased time to recovery.模拟分娩损伤的持续时间增加会导致恢复时间延长。
Am J Physiol Regul Integr Comp Physiol. 2007 Apr;292(4):R1738-44. doi: 10.1152/ajpregu.00784.2006. Epub 2007 Jan 4.
9
Monocyte chemotactic protein-3 is a myocardial mesenchymal stem cell homing factor.单核细胞趋化蛋白-3是一种心肌间充质干细胞归巢因子。
Stem Cells. 2007 Jan;25(1):245-51. doi: 10.1634/stemcells.2006-0293. Epub 2006 Oct 19.
10
Risk of urinary incontinence after childbirth: a 10-year prospective cohort study.产后尿失禁的风险:一项为期10年的前瞻性队列研究。
Obstet Gynecol. 2006 Oct;108(4):873-8. doi: 10.1097/01.AOG.0000233172.96153.ad.

近交系大鼠模拟分娩损伤

Simulated childbirth injuries in an inbred rat strain.

作者信息

Woo Lynn L, Hijaz Adonis, Pan Hui Q, Kuang Mei, Rackley Raymond R, Damaser Margot S

机构信息

The Glickman Urological Institute, Cleveland Clinic, Cleveland, Ohio 44195, USA.

出版信息

Neurourol Urodyn. 2009;28(4):356-61. doi: 10.1002/nau.20644.

DOI:10.1002/nau.20644
PMID:18973147
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2668733/
Abstract

AIMS

Vaginal distension (VD) in outbred rats has been shown to decrease urethral resistance, as well as increase the expression of the stem cell-homing chemokine, monocyte chemotactic factor 3 (MCP-3), but not stromal derived factor 1 (SDF-1). The aim of this study was to determine if similar responses are induced by VD in an inbred rat strain.

METHODS

Forty female Lewis rats underwent VD or sham VD followed by leak point pressure (LPP) testing 4 or 10 days later. Ten additional rats served as controls. The urethra and vagina were then dissected for histology. To examine chemokine expression, eight additional rats underwent VD with organs harvested immediately or 1 day after the procedure for reverse transcriptase polymerase chain reaction (RT-PCR) of MCP-3 and SDF-1. Four age-matched rats served as controls.

RESULTS

Four days after VD, LPP was significantly lower in VD rats (14.3 +/- 1.6 cm H(2)O) than controls (18.7 +/- 1.3 cm H(2)O). Ten days after VD, LPP in both VD (19.7 +/- 2.6 cm H(2)O) and sham (18.4 +/- 1.3 cm H(2)O) groups was not significantly different from controls. Urethral histology demonstrated marked disruption and atrophy of smooth and striated muscle in VD rats compared to shams and controls. RT-PCR yielded a 25-fold significant increase in expression of urethral MCP-3 immediately following VD. SDF-1 was significantly decreased in the urethra and vagina immediately after VD and in the bladder 24 hr after VD.

CONCLUSION

VD in Lewis rats produces functional, histological and molecular results similar to that of outbred rats. This model could be utilized in future studies investigating cellular transplant methods of improving urethral function.

摘要

目的

已表明远交系大鼠的阴道扩张(VD)可降低尿道阻力,并增加干细胞归巢趋化因子单核细胞趋化因子3(MCP-3)的表达,但不会增加基质细胞衍生因子1(SDF-1)的表达。本研究的目的是确定VD在近交系大鼠品系中是否诱导类似反应。

方法

40只雌性Lewis大鼠接受VD或假VD,4或10天后进行漏点压力(LPP)测试。另外10只大鼠作为对照。然后解剖尿道和阴道进行组织学检查。为了检查趋化因子表达,另外8只大鼠接受VD,在手术后立即或1天后收获器官,用于MCP-3和SDF-1的逆转录聚合酶链反应(RT-PCR)。4只年龄匹配的大鼠作为对照。

结果

VD后4天,VD大鼠的LPP(14.3±1.6 cm H₂O)显著低于对照组(18.7±1.3 cm H₂O)。VD后10天,VD组(19.7±2.6 cm H₂O)和假手术组(18.4±1.3 cm H₂O)的LPP与对照组无显著差异。与假手术组和对照组相比,VD大鼠的尿道组织学显示平滑肌和横纹肌明显破坏和萎缩。VD后立即进行RT-PCR显示尿道MCP-3表达显著增加25倍。VD后立即尿道和阴道以及VD后24小时膀胱中的SDF-1显著降低。

结论

Lewis大鼠的VD产生与远交系大鼠相似的功能、组织学和分子结果。该模型可用于未来研究改善尿道功能的细胞移植方法。