Department of Urology, Nara Medical University, Kashihara, Japan.
Department of Urology, Kindai University Nara Hospital, Ikoma, Japan.
Neurourol Urodyn. 2018 Nov;37(8):2434-2440. doi: 10.1002/nau.23715. Epub 2018 May 24.
We investigated the role of the bladder wall in permeating water, focusing on aquaporins.
Female Sprague-Dawley rats weighing 300 g were used to investigate the role of the bladder wall in saline permeation. Changes in intravesical fluid volume and sodium concentration were measured in the desmopressin acetate hydrate-loaded and control groups 3 h after administration. Bladders were resected to measure aquaporin-1, 2, and 3 gene expression using qRT-PCR. Additionally, the change of aquaporin-2 expression was measured using Western blotting and immunohistochemistry in intravesical aquaporin-2 siRNA-treated and control groups.
Although the intravesical fluid volume and sodium concentration significantly decreased from 0 to 3 h (1.00 ± 0.00 vs 0.83 ± 0.08 mL, 157.80 ± 1.30 vs 146.8 ± 1.92 mEq/mL, P < 0.01, respectively in the control group), administration of desmopressin did not affect the extent of volume change. Aquaporin-2 expression was significantly higher in the 3-h distended bladders than in the empty bladder. Aquaporin-2 siRNA treatment suppressed aquaporin-2 expression and the change of intravesical fluid volume from 0 to 3 h (1.00 ± 0.00 and 0.99 ± 0.02 mL), which was related to the suppression of sodium concentration change in comparison with control siRNA treatment (149.6 ± 2.4 vs 143.6 ± 3.67 mEq/mL, P < 0.05).
The rat urinary bladder absorbs water and salts under the full-filled condition. Aquaporin-2 plays an important role in the transport of water, accompanied by sodium concentration change. We demonstrated a part of the bladder absorption mechanism, which may lead to development of a new method for regulating bladder storage function.
我们研究了膀胱壁在渗透水中的作用,重点研究水通道蛋白。
使用 300g 雌性 Sprague-Dawley 大鼠研究膀胱壁在盐渗透中的作用。在给予去氨加压素水合物负荷后 3 小时,测量去氨加压素组和对照组膀胱内液体积和钠浓度的变化。切除膀胱,使用 qRT-PCR 测量水通道蛋白-1、2 和 3 的基因表达。此外,在膀胱内水通道蛋白-2 siRNA 处理组和对照组中,使用 Western 印迹和免疫组织化学测量水通道蛋白-2 表达的变化。
尽管与 0 小时相比,膀胱内液体积和钠浓度在 3 小时时明显下降(对照组中分别为 1.00±0.00 与 0.83±0.08mL,157.80±1.30 与 146.8±1.92mEq/mL,P<0.01),但给予去氨加压素并未影响体积变化的程度。在 3 小时扩张的膀胱中,水通道蛋白-2 的表达明显高于空虚的膀胱。水通道蛋白-2 siRNA 处理抑制了水通道蛋白-2 的表达以及从 0 小时到 3 小时的膀胱内液体积变化(分别为 1.00±0.00 与 0.99±0.02mL),与对照 siRNA 处理相比,这与抑制钠浓度变化有关(分别为 149.6±2.4 与 143.6±3.67mEq/mL,P<0.05)。
在完全充盈的情况下,大鼠的膀胱吸收水和盐。水通道蛋白-2 在水的转运中起重要作用,同时伴随着钠浓度的变化。我们证明了膀胱吸收机制的一部分,这可能为调节膀胱储存功能的新方法的发展提供了依据。