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布美他尼诱导大鼠纹状体内间隙增大及血管加压素2型拮抗剂的作用

Bumetanide-induced enlargement of the rat intrastrial space and effects of a vasopressin type 2 antagonist.

作者信息

Nishimura Masahiko, Kakigi Akinobu, Takeda Taizo, Okada Teruhiko, Doi Katsumi

机构信息

Department of Otolaryngology, Osaka University Graduate School of Medicine, Osaka, Japan.

出版信息

ORL J Otorhinolaryngol Relat Spec. 2010;71 Suppl 1:10-5. doi: 10.1159/000265114. Epub 2010 Feb 24.

Abstract

OBJECTIVE

Water homeostasis is essential for the inner ear to maintain the function of hearing and equilibrium. Bumetanide inhibits Na(+)-K(+)-2Cl(-) co-transporter (NKCC), which is expressed in the basolateral membrane of stria vascularis marginal cell, and it causes the enlargement of intrastrial space. Aquaporin (AQP) 2 is expressed in the perilymph side of stria vascularis basal cell, and the vasopressin type 2 antagonist OPC-31260 produces downregulation of AQP2 mRNA levels in the inner ear. The aim of this study is to investigate the influence of OPC-31260 on experimentally induced enlargement of the intrastrial space caused by bumetanide.

MATERIALS AND METHODS

Wistar rats were divided into two groups, a BUM group and an OPC-BUM group. The BUM group was exposed to bumetanide, and the OPC-BUM group was exposed to bumetanide after being premedicated with OPC-31260. The specimens of the stria vascularis were observed using transmission electron microscopy and analyzed quantitatively and statistically.

RESULTS

Morphological changes of intrastrial space enlargement occurred in both the BUM and OPC-BUM groups. The ratio of the areas of the intrastrial space area to the stria vascularis were calculated, and the OPC-BUM group mean showed a minimal difference from the BUM-group mean. However, there is no statistical difference.

CONCLUSIONS

Premedication of rats with OPC-31260 tended to reduce bumetanide-induced enlargement of the intrastrial space. This may indicate that the effect of bumetanide on the stria vascularis is much stronger than that of OPC-31260.

摘要

目的

水稳态对于内耳维持听力和平衡功能至关重要。布美他尼抑制钠-钾-2氯协同转运蛋白(NKCC),该蛋白表达于血管纹边缘细胞的基底外侧膜,它会导致纹状体内间隙增大。水通道蛋白(AQP)2表达于血管纹基底细胞的外淋巴侧,2型血管加压素拮抗剂OPC-31260会使内耳中AQP2 mRNA水平下调。本研究的目的是探讨OPC-31260对布美他尼实验性诱导的纹状体内间隙增大的影响。

材料与方法

将Wistar大鼠分为两组,布美他尼组(BUM组)和OPC-布美他尼组(OPC-BUM组)。BUM组给予布美他尼,OPC-BUM组在预先给予OPC-31260后给予布美他尼。使用透射电子显微镜观察血管纹标本,并进行定量和统计学分析。

结果

BUM组和OPC-BUM组均出现了纹状体内间隙增大的形态学变化。计算纹状体内间隙面积与血管纹面积的比值,OPC-BUM组的平均值与BUM组的平均值差异最小。然而,无统计学差异。

结论

用OPC-31260对大鼠进行预处理倾向于减少布美他尼诱导的纹状体内间隙增大。这可能表明布美他尼对血管纹的作用比OPC-3所260强得多。

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