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[5型磷酸二酯酶抑制剂对膀胱过度活动症大鼠的作用及机制]

[Effects and mechanisms of phosphodiesterase type 5 inhibitors on rats with overactive bladder].

作者信息

Chen Hong-de, Ye Xue-ting, Weng Zhi-liang, Li Cheng-di

机构信息

Department of Urology, Wenzhou Medical College, Wenzhou, China.

出版信息

Zhonghua Yi Xue Za Zhi. 2011 Jul 26;91(28):2001-5.

Abstract

OBJECTIVE

To investigate the effects and the possible mechanistic pathway of phosphodiesterase type 5 (PDE5) inhibitors on rats with overactive bladder.

METHODS

A total of 24 adult male spontaneously hypertensive rats (SHRs) were randomly divided into 3 groups: daily lavage group, discontinuous lavage group and blank group (n = 8 each). Daily vardenafil (10 mg×kg(-1)×d(-1)), discontinuous vardenafil (10 mg×kg(-1)×d(-1)) and daily normal saline were administered respectively to 3 groups by lavage. And 8 adult male SD rats were included into the control group. Bladder urodynamic examinations were conducted in each group 2 weeks later. Then bladder detrusor muscle strips isolated from each group were further divided into two parts. One part was first pre-contracted and then the relaxant effects of sodium nitroprusside and Y-27632 were observed. For another part, enzyme-linked immunosorbent assay was used to measure cyclic guanosine monophosphate (cGMP).

RESULTS

As compared with the control group, the values of bladder inter contraction interval (ICI) and bladder capacity (BC) were significantly lower [(409 ± 36) s vs (568 ± 60) s, (284 ± 25) µl vs (395 ± 42) µl, P < 0.01] while the bladder non voiding contraction (NVC) was significantly higher in the blank group [(2.03 ± 0.49) number/min vs(1.07 ± 0.30) number/min, P < 0.01]. Compared with the blank group, the values of ICI and BC were elevated. NVC decreased obviously in the discontinues and daily lavage groups [(486 ± 53) s and (564 ± 44) s; (337 ± 37) µl and (392 ± 30) µl; (1.82 ± 0.32) number/min and (0.52 ± 0.23) number/min, P < 0.05]. The effects were more significant in the daily lavage group (P < 0.01). The maximal relaxant effect of sodium nitroprusside was obviously enhanced in the discontinues and daily lavage groups [(50.6 ± 2.1)% and (67.9 ± 4.1)% vs(25.3 ± 5.0)%, P < 0.01]. However the sensitivity of Y-27632 decreased significantly [(35.8 ± 2.5)% and (20.2 ± 2.3)% vs (71.6 ± 2.8)%, P < 0.01], while the level of cGMP was significantly higher in the bladder detrusor muscle [(20.6 ± 4.1) fmol/mg and (29.4 ± 4.3) fmol/mg vs (12.9 ± 2.1) fmol/mg, P < 0.01]. The effects of the daily lavage group were more pronounced (P < 0.01).

CONCLUSION

The phenomenon of bladder overactivity is observed in the SHRs. The PDE5 inhibitors are effective in treating overactive bladder. And the effect of daily supplement is much better. In addition, the mechanism may operate through the cGMP-dependent protein kinase G-RhoA/Rho kinase signaling pathway.

摘要

目的

探讨5型磷酸二酯酶(PDE5)抑制剂对膀胱过度活动症大鼠的影响及其可能的作用机制途径。

方法

将24只成年雄性自发性高血压大鼠(SHRs)随机分为3组:每日灌洗组、间断灌洗组和空白组(每组8只)。分别对3组大鼠每日灌胃给予伐地那非(10 mg×kg⁻¹×d⁻¹)、间断给予伐地那非(10 mg×kg⁻¹×d⁻¹)和每日给予生理盐水。另取8只成年雄性SD大鼠作为对照组。2周后对每组大鼠进行膀胱尿动力学检查。然后将每组分离的膀胱逼尿肌条进一步分为两部分。一部分先进行预收缩,然后观察硝普钠和Y-27632的舒张作用。另一部分采用酶联免疫吸附测定法检测环磷酸鸟苷(cGMP)。

结果

与对照组相比,空白组膀胱收缩间期(ICI)和膀胱容量(BC)值显著降低[(409±36)s对(568±60)s,(284±25)μl对(395±42)μl,P<0.01],而膀胱无抑制性收缩(NVC)显著升高[(2.03±0.49)次/分钟对(1.07±0.30)次/分钟,P<0.01]。与空白组相比,间断灌洗组和每日灌洗组的ICI和BC值升高,NVC明显降低[(486±53)s和(564±44)s;(337±37)μl和(392±30)μl;(1.82±0.32)次/分钟和(0.52±0.23)次/分钟,P<0.05]。每日灌洗组效果更显著(P<0.01)。间断灌洗组和每日灌洗组硝普钠的最大舒张作用明显增强[(50.6±2.1)%和(67.9±4.1)%对(25.3±5.0)%,P<0.01]。然而,Y-27632的敏感性显著降低[(35.8±2.5)%和(20.2±2.3)%对(71.6±2.8)%,P<0.01],而膀胱逼尿肌中cGMP水平显著升高[(20.6±4.1)fmol/mg和(29.4±4.3)fmol/mg对(12.9±2.1)fmol/mg,P<0.01]。每日灌洗组效果更明显(P<0.01)。

结论

在SHRs中观察到膀胱过度活动现象。PDE5抑制剂对治疗膀胱过度活动症有效。每日补充的效果更好。此外,其作用机制可能通过cGMP依赖性蛋白激酶G-RhoA/Rho激酶信号通路发挥作用。

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