血压的性别差异与小鼠肾脏钠离子通道的关系
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国家自然科学基金(81300709);浙江省自然科学基金(LY13H070007)。


Relationship between gender difference of blood pressure and sodium ion channels in the kidney of mice
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    摘要:

    目的 研究雌雄小鼠的血压、肾脏尿钠排泄以及相关的肾脏钠离子通道和信号通路,初步探讨血压的性别差异与肾脏钠离子通道的关系。方法 选取成年雌雄小鼠,用无创血压仪检测小鼠血压,火焰分光光度计测量小鼠血、尿钠离子浓度,Real-time PCR和Western-Blot检测小鼠肾脏钠氯同向转运体(NCC)、钠钾氯同向转运体(NKCC2)、上皮钠离子通道(ENaC)的表达水平,以及上游的缺乏赖氨酸的丝氨酸苏氨酸蛋白激酶(WNK激酶)的mRNA水平。结果 雌鼠血压低于雄鼠,尿钠排泄高于雄鼠,NCC、NKCC2的mRNA和蛋白水平均明显增加,ENaC无明显差异,WNK4显著升高,WNK1无差异。结论 雌鼠血压低于雄鼠可能是由雌鼠尿钠排泄增加导致,WNK4-NCC/NKCC2信号通路参与其调控。

    Abstract:

    Objective Study on the blood pressure, renal sodium excretion, related renal sodium ion channels and signaling pathways between male and female mice, to investigate the relationship between gender differences in blood pressure and renal sodium ion channel.Methods Blood pressure of adult female and male mice was measured using tail-cuff sphygmomanometer. Plasma and urine electrolytes were performed using flame photometer.Protein levels of renal sodium transporters NCC, NKCC2, ENaC were determined by western blot, mRNA levels of these transporters and the upstream With No lysine (WNK) kinases were determined by Real-time PCR.Results The blood pressure of female mice was significantly lower than that of male mice. Renal sodium excretion and mRNA levels of NCC&NKCC2 were increased significantly in female mice. No obvious difference was observed in ENaC. The mRNA level of WNK4 was increased while no change in WNK1.Conclusions The lower blood pressure of female mice may caused by increasing renal sodium excretion and WNK4-NCC/NKCC2 signaling pathway involved.

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王伟,俞国峰,程梦婷,赵蓉,刘珍.血压的性别差异与小鼠肾脏钠离子通道的关系[J].中国比较医学杂志,2016,26(9):13~18.

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  • 最后修改日期:2016-03-30
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  • 在线发布日期: 2016-09-22
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