Department of Urology, Xijing Hospital, Xi'an, China.
BJU Int. 2013 May;111(5):843-51. doi: 10.1111/j.1464-410X.2012.11408.x. Epub 2012 Aug 9.
WHAT'S KNOWN ON THE SUBJECT? AND WHAT DOES THE STUDY ADD?: In the urinary bladder, histological studies suggest a network of functionally connected interstitial cells of Cajal (ICCs) are located between the urothelium and sensory nerve endings, which might transfer signals directly between them. Purinergic P2X3 receptors may play roles in the micturition reflex pathway, and its expression profiles in ICCs could be altered in urinary bladder dysfunction. The present experiments showed a novel time-dependent P2X3 receptor up-regulation in ICCs in an experimental rat model of partial bladder outlet obstruction.
To investigate the expression and electrophysiological characteristics of purinergic P2X3 receptors in interstitial cells of Cajal (ICCs) at different time points after partial bladder outlet obstruction (PBOO) in rats.
In all, 48 female Sprague-Dawley rats were randomly divided into four groups: 4, 6 and 8 week PBOO groups and sham-operated controls. At 4 weeks after surgery, cystometry was performed to investigate bladder function in vivo. Subsequently, the rats were humanely killed at 4, 6 or 8 weeks and the bladders were harvested for measurements. P2X3 expression in ICCs of bladder was investigated by immunofluorescent staining. The level of P2X3 mRNA was detected by reverse transcription-polymerase chain reaction (RT-PCR). Inward currents in corresponding ICCs after PBOO were investigated electrophysiologically.
Cystometrography showed a valid increase in maximum detrusor pressure in rats subjected to PBOO. The bladder weight in the PBOO group was significantly higher than that in the control group. In contrast to sham rats, there was a significant increase in the intensity of P2X3 staining in the ICCs in all PBOO groups. C-kit labelled isolated ICCs were strongly stained with the P2X3 antibody. RT-PCR showed that the expression of P2X3 mRNA was significantly up-regulated at 4, 6 and 8 weeks in the ICCs from the PBOO rats. In the ICCs, the mean peak amplitude of inward currents was significantly increased in the PBOO groups compared with the control group.
The expression of P2X3 receptors showed a time dependent up-regulation in the ICCs of the bladder in rats with PBOO. PBOO induced the potentiation of P2X3 receptors function, as evidenced by α, β-methylene ATP-enhanced inward currents in the ICCs of the rat bladder.
研究在大鼠部分膀胱出口梗阻(PBOO)后不同时间点,缝隙连接细胞(ICCs)中嘌呤能 P2X3 受体的表达和电生理特征。
48 只雌性 Sprague-Dawley 大鼠随机分为 4 组:4、6 和 8 周 PBOO 组和假手术对照组。术后 4 周行膀胱测压术,观察大鼠体内膀胱功能。随后,在 4、6 或 8 周时将大鼠处死并取出膀胱进行测量。通过免疫荧光染色研究 ICCs 中 P2X3 的表达。通过逆转录聚合酶链反应(RT-PCR)检测 P2X3 mRNA 的水平。通过电生理方法研究 PBOO 后 ICCs 中的内向电流。
膀胱测压显示 PBOO 大鼠最大逼尿肌压明显升高。PBOO 组膀胱重量明显高于对照组。与假手术组大鼠相比,所有 PBOO 组 ICCs 中 P2X3 染色强度均显著增加。C-kit 标记的分离 ICCs 与 P2X3 抗体强烈染色。RT-PCR 显示,PBOO 大鼠 ICCs 中 P2X3 mRNA 的表达在 4、6 和 8 周时均显著上调。在 ICCs 中,与对照组相比,PBOO 组内向电流的平均峰值幅度明显增加。
在 PBOO 大鼠的 ICCs 中,P2X3 受体的表达呈时间依赖性上调。PBOO 诱导 P2X3 受体功能增强,表现为大鼠膀胱 ICCs 中α、β-亚甲基 ATP 增强的内向电流。