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盆腔器官脱垂赖氨酰氧化酶样-1基因敲除小鼠的膀胱和尿道功能

Bladder and urethral function in pelvic organ prolapsed lysyl oxidase like-1 knockout mice.

作者信息

Liu Guiming, Daneshgari Firouz, Li Mei, Lin Danli, Lee Una, Li Tiansen, Damaser Margot S

机构信息

Glickman Urological Institute & Department of Biomedical Engineering, Cleveland Clinic, Cleveland, OH 44195, USA.

出版信息

BJU Int. 2007 Aug;100(2):414-8. doi: 10.1111/j.1464-410X.2007.06929.x. Epub 2007 Jun 6.

Abstract

OBJECTIVES

To examine bladder and urethral function in pelvic organ prolapsed lysyl oxidase like-1 (LOXL1) knockout mice.

MATERIALS AND METHODS

Female parous Loxl1 (-/-) mice in the stable phase of prolapse, and age-matched wild type (WT) mice (six each) had conscious cystometry, leak-point pressure (LPP) testing, and contractile responses assessed of their bladder muscle strips to KCl, electrical-field stimulation, ATP, and carbachol.

RESULTS

Loxl1 (-/-) mice voided more frequently and had lower mean (sem) bladder capacity, at 0.10 (0.01) vs 0.20 (0.01) mL, and voiding pressure, at 25.0 (1.90) vs 36.6 (4.04) cmH(2)O, respectively, during cystometry than had WT mice. The LPP was not significantly different between WT and Loxl1 (-/-) mice, at 7.05 (0.81) vs 5.22 (1.23) cmH(2)O, respectively. There were no significant differences between bladder strips from Loxl1 (-/-) mice and WT mice in their responsiveness to various stimuli.

CONCLUSIONS

Loxl1 (-/-) knockout mice had lower urinary tract dysfunction, most likely due to urethral dysfunction. Loxl1 (-/-) knockout mice can be used as an animal model for pelvic floor disorders. Further studies are needed to characterize the morphological and molecular alterations of the bladder and urethra.

摘要

目的

研究盆腔器官脱垂赖氨酰氧化酶样1(LOXL1)基因敲除小鼠的膀胱和尿道功能。

材料与方法

处于脱垂稳定期的经产雌性Loxl1(-/-)小鼠和年龄匹配的野生型(WT)小鼠(各6只)进行清醒膀胱测压、漏点压力(LPP)测试,并评估其膀胱肌条对氯化钾、电场刺激、三磷酸腺苷(ATP)和卡巴胆碱的收缩反应。

结果

在膀胱测压期间,Loxl1(-/-)小鼠排尿更频繁,平均(标准误)膀胱容量更低,分别为0.10(0.01)mL和0.20(0.01)mL,排尿压力也更低,分别为25.0(1.90)cmH₂O和36.6(4.04)cmH₂O。WT小鼠和Loxl1(-/-)小鼠的LPP无显著差异,分别为7.05(0.81)cmH₂O和5.22(1.23)cmH₂O。Loxl1(-/-)小鼠和WT小鼠的膀胱肌条对各种刺激的反应性无显著差异。

结论

Loxl1(-/-)基因敲除小鼠存在较低程度的尿路功能障碍,最可能是由于尿道功能障碍。Loxl1(-/-)基因敲除小鼠可作为盆底功能障碍的动物模型。需要进一步研究来明确膀胱和尿道的形态及分子改变。

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