Department of Urology, Fukushima Medical University, Fukushima, Japan.
Neurourol Urodyn. 2011 Mar;30(3):461-7. doi: 10.1002/nau.20984. Epub 2010 Sep 30.
Using a rat BOO model, we determined whether α1-adrenoceptor (AR) antagonists (silodosin, prazosin) improve the bladder storage function by reducing afferent input from the lower urinary tract.
Male rats received partial bladder outlet obstruction or sham surgery were used. Four weeks following surgery, their voiding behavior was measured in a metabolic cage. BOO-rats were administered silodosin, prazosin or vehicle for 2 weeks subcutaneously using osmotic pump. At the post-drug condition, voiding behavior was measured again. The L6 spinal cord was removed and immunostained using anti c-Fos antibody. The rats were also performed continuous cystometry with saline without anesthesia or restraint at the pre- and post-drug conditions.
Metabolic cage study showed the voiding behavior of BOO-rats was characterized by increase in frequency of urination and decrease in volume voided. Cystometric evaluation also showed the significant increase both in the number of successive voiding contraction and in contraction pressure. The administration of silodosin or prazosin significantly decreased urinary frequency and the number of micturition reflex but affected neither bladder contraction pressure nor residual volume. The number of c-Fos-positive cell significantly increased in BOO-rats, while significantly decreased in those receiving αl-AR antagonists.
The present study demonstrates that α1-AR antagonists silodosin and prazosin have an inhibitory effect on afferent input from the lower urinary tract independently of reducing urethral resistance, and thereby reduce the storage dysfunction secondary to BOO. This result suggests that αl-AR, particularly αlA-AR, may play an important role in the activation of the afferent pathway.
通过减少来自下尿路的传入输入,我们使用大鼠 BOO 模型来确定 α1-肾上腺素能受体 (AR) 拮抗剂(西洛多辛、哌唑嗪)是否通过改善膀胱存储功能。
雄性大鼠接受部分膀胱出口梗阻或假手术。手术后 4 周,在代谢笼中测量其排尿行为。BOO 大鼠接受西洛多辛、哌唑嗪或载体皮下给药 2 周,使用渗透泵。在药物治疗后,再次测量排尿行为。取出 L6 脊髓并用抗 c-Fos 抗体进行免疫染色。在药物治疗前后,在没有麻醉或束缚的情况下,用生理盐水对大鼠进行连续膀胱测压。
代谢笼研究表明,BOO 大鼠的排尿行为表现为排尿频率增加和排尿量减少。膀胱测压评估还显示,连续排尿收缩的次数和收缩压都显著增加。西洛多辛或哌唑嗪的给药显著减少了尿频率和排尿反射次数,但对膀胱收缩压或残余尿量没有影响。c-Fos 阳性细胞的数量在 BOO 大鼠中显著增加,而在接受 α1-AR 拮抗剂的大鼠中则显著减少。
本研究表明,α1-AR 拮抗剂西洛多辛和哌唑嗪对来自下尿路的传入输入具有抑制作用,独立于降低尿道阻力,从而减轻 BOO 引起的存储功能障碍。这一结果表明,α1-AR,特别是 α1A-AR,可能在传入途径的激活中发挥重要作用。