Folasire Oladayo S, Chess-Williams Russ, Sellers Donna J
Centre for Urology Research, Faculty of Health Sciences and Medicine, Bond University, Gold Coast, Qld, Australia.
Clin Exp Pharmacol Physiol. 2017 Sep;44(9):954-960. doi: 10.1111/1440-1681.12779.
The urethral uroepithelium has been implicated in urethral sensation and maintenance of continence. However, relatively little is known about the function of the urethral urothelium compared with that of the bladder. The aim of the study was to examine the role of the urothelium/lamina propria on contractility of the porcine urethra, along with the influence of nitric oxide, prostaglandins and ageing. Porcine urethral tissues, intact and denuded of urothelium/lamina propria, were mounted in tissue baths and contractions to noradrenaline, phenylephrine and carbachol obtained. Contractions in the presence of Nώ-nitro-l-arginine (100 μmol/L) and indomethacin (10 μmol/L) were examined, along with contractions of tissues from young (6 months) and older (3 years) animals. The urothelium/lamina propria of the urethra significantly inhibited contractions to carbachol, noradrenaline and phenylephrine. This inhibitory effect was not significantly different for the three agonists (58.7±10.3%, 60.4±12.6% and 39.4±12.2% inhibition; n=4-7), and was also observed when denuded tissues were co-incubated with a second tissue with intact urothelium/lamina propria (40.6±7.5% inhibition; n=6). Inhibition of nitric oxide and prostaglandin production did not attenuate the inhibitory effect of the urothelium/lamina propria on noradrenaline contractions. In addition, ageing did not alter the inhibitory effect for either phenylephrine contractions (33.9±2.2% vs 41.0±9.7%, young vs older urethral tissues) or noradrenaline contractions (32.9±11.1% vs 53.7±11.0%). In conclusion the urothelium/lamina propria of the urethra has an inhibitory effect on receptor-mediated urethral contraction. This inhibition is due to the release of a diffusible factor, and the effect is not mediated by nitric oxide or prostaglandins, or affected by age.
尿道尿路上皮与尿道感觉及控尿维持有关。然而,与膀胱尿路上皮相比,人们对尿道尿路上皮功能的了解相对较少。本研究旨在探讨尿路上皮/固有层对猪尿道收缩性的作用,以及一氧化氮、前列腺素和衰老的影响。将完整的以及去除尿路上皮/固有层的猪尿道组织置于组织浴槽中,记录其对去甲肾上腺素、苯肾上腺素和卡巴胆碱的收缩反应。检测在存在Nω-硝基-L-精氨酸(100 μmol/L)和吲哚美辛(10 μmol/L)时的收缩情况,以及来自年轻(6个月)和年长(3岁)动物组织的收缩情况。尿道的尿路上皮/固有层显著抑制对卡巴胆碱、去甲肾上腺素和苯肾上腺素的收缩反应。这三种激动剂的抑制作用无显著差异(抑制率分别为58.7±10.3%、60.4±12.6%和39.4±12.2%;n = 4 - 7),并且当去除上皮的组织与另一个具有完整尿路上皮/固有层的组织共同孵育时也观察到了这种抑制作用(抑制率为40.6±7.5%;n = 6)。抑制一氧化氮和前列腺素的产生并未减弱尿路上皮/固有层对去甲肾上腺素收缩反应的抑制作用。此外,衰老并未改变对苯肾上腺素收缩反应(年轻与年长尿道组织分别为33.9±2.2%对41.0±9.7%)或去甲肾上腺素收缩反应(分别为32.9±11.1%对53.7±11.0%)的抑制作用。总之,尿道的尿路上皮/固有层对受体介导的尿道收缩具有抑制作用。这种抑制作用是由于一种可扩散因子的释放,且该作用并非由一氧化氮或前列腺素介导,也不受年龄影响。