Adenosine Receptor Mechanisms Underlying Bladder Dysfunction in Male Rats With Bladder Outlet Obstruction.

IF 1.8 3区 医学 Q3 UROLOGY & NEPHROLOGY
Ei-Ichiro Takaoka, Masahiro Kurobe, Kanako Matsuoka, Tadanobu Kamijo, Shingo Kimura, Paul N Watton, Anne M Robertson, Naoki Yoshimura
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Abstract

Aims: We examined the role of subtypes of adenosine receptors in bladder dysfunction and changes in the adenosine receptor expression in the bladder using male rats with partial bladder outlet obstruction (BOO).

Methods: In Sprague-Dawley rats (male 8-weeks old), BOO was produced by a partial ligation of the urethra along a metal rod of a 1.2 mm outer diameter. Control rats underwent sham operation. Awake cystometrograms (CMG) were first recorded during saline instillation, and then an adenosine A1 receptor agonist (CCPA, 4.1 μM), an adenosine A2A antagonist (ZM241385, 15 μM), or inosine (1 mM) were applied intravesically in sham and BOO rats. In addition, mRNA levels of adenosine receptor subtypes in the bladder wall were measured using RT-PCR. Histological studies of bladder specimen were also performed.

Results: Weights of BOO bladders were significantly (p < 0.0001) larger compared with sham bladders. In CMG, a number of non-voiding contractions (NVCs), bladder contraction amplitudes during voiding, bladder capacity, and post-void residual (PVR) were significantly (p < 0.001) increased compared with sham rats. Voiding efficiency (VE) was significantly (p < 0.001) reduced in BOO versus sham rats. Intravesical application of CCPA or inosine did not induce statistically significant effects on CMG parameters in BOO rats. Yet, ZM241385 induced a significant (p = 0.040) reduction in NVCs of BOO rats. mRNA levels of adenosine A2A and A3 receptors were significantly (p < 0.0001 and p = 0.0145, respectively) upregulated in the BOO bladder mucosa, whereas adenosine A2B receptors showed a significant (p < 0.0001) reduction in the BOO bladder mucosa compared with sham bladders. Histologically, we found the thickened detrusor muscle layer in BOO versus sham rats.

Conclusions: The male rat model of BOO seems to be suitable for exploring urethral obstruction-related bladder dysfunction at the compensated phase. In addition, the adenosine A2A receptor subtype would be a potential target for the treatment of male BOO patients with bladder overactivity.

Clinical trial registration: A clinical trial registration is not required as this study reported the basic research data using animal models.

膀胱出口梗阻雄性大鼠膀胱功能障碍的腺苷受体机制。
目的:以部分膀胱出口梗阻(BOO)的雄性大鼠为实验对象,研究腺苷受体亚型在膀胱功能障碍中的作用和膀胱腺苷受体表达的变化。方法:在Sprague-Dawley大鼠(雄性8周龄)中,通过沿外径1.2 mm的金属棒部分结扎尿道产生BOO。对照大鼠进行假手术。在生理盐水灌注期间记录清醒膀胱图(CMG),然后在sham和BOO大鼠体内注射腺苷A1受体激动剂(CCPA, 4.1 μM)、腺苷A2A拮抗剂(ZM241385, 15 μM)或肌苷(1 mM)。此外,采用RT-PCR检测膀胱壁腺苷受体亚型mRNA水平。膀胱标本的组织学研究也进行了。结论:BOO雄性大鼠模型似乎适合于探索代偿期尿道梗阻相关性膀胱功能障碍。此外,腺苷A2A受体亚型可能是治疗膀胱过度活动的男性BOO患者的潜在靶点。临床试验注册:本研究采用动物模型报道基础研究数据,不需要进行临床试验注册。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Neurourology and Urodynamics
Neurourology and Urodynamics 医学-泌尿学与肾脏学
CiteScore
4.30
自引率
10.00%
发文量
231
审稿时长
4-8 weeks
期刊介绍: Neurourology and Urodynamics welcomes original scientific contributions from all parts of the world on topics related to urinary tract function, urinary and fecal continence and pelvic floor function.
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