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水通道蛋白-2在大鼠膀胱壁水转运中起重要作用。

Aquaporin-2 plays an important role in water transportation through the bladder wall in rats.

机构信息

Department of Urology, Nara Medical University, Kashihara, Japan.

Department of Urology, Kindai University Nara Hospital, Ikoma, Japan.

出版信息

Neurourol Urodyn. 2018 Nov;37(8):2434-2440. doi: 10.1002/nau.23715. Epub 2018 May 24.

Abstract

AIM

We investigated the role of the bladder wall in permeating water, focusing on aquaporins.

METHODS

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.

RESULTS

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).

CONCLUSIONS

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.

摘要

目的

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。

方法

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。

结果

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)。

结论

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。

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