钙调磷酸酶/活化T细胞因子信号通路在有氧运动诱导高血压大鼠血管平滑肌细胞KV2.1通道表达上调中的作用
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(北京体育大学运动与体质健康教育部重点实验室,北京市 100084)

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李珊珊,博士研究生,研究方向为运动和心血管生理学,E-mail为124914818@qq.com。通信作者石丽君,博士,教授,博士研究生导师,研究方向为运动和心血管生理学,E-mail为l_j_shi72@163.com。

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国家自然科学基金项目(31771312);北京市自然科学基金项目(5172023)


The role of CaN/NFAT signaling pathway in aerobic exercise-induced upregulation of KV2.1 channels in vascular smooth muscle cells in hypertension rat
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Key Laboratory of Physical Fitness and Exercise, Ministry of Education, Beijing Sport University, Beijing 100084, China)

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    摘要:

    目的 探讨钙调磷酸酶/活化T细胞因子(CaN/NFAT)信号通路在有氧运动诱导原发性高血压大鼠(SHR)肠系膜动脉血管平滑肌细胞电压依赖性钾通道(KV2.1)表达上调中的作用。方法 选用3月龄雄性WKY和SHR大鼠各24只,随机分为WKY安静组和运动组(WKY-SED组、WKY-EX组)、SHR安静组和运动组(SHR-SED组、SHR-EX组)。运动干预前和12周运动结束后分别测量大鼠安静状态下的心率和血压。分别采用免疫组化和Western blot检测KV2.1、CaN在肠系膜动脉的分布以及KV2.1、CaN、p-NFATc3、A型激酶锚定蛋白(AKAP150)和钙调蛋白(CaM)的蛋白表达。结果 (1)12周有氧运动后,与SHR-SED组相比,SHR-EX组心率、收缩压和平均动脉压均显著降低(P<0.01);与WKY-SED组相比,WKY-EX组收缩压显著降低(P<0.05)。(2)与WKY-SED组相比,SHR-SED组KV2.1在肠系膜动脉的蛋白表达显著减少(P<0.01);与SHR-SED组相比,SHR-EX组KV2.1的蛋白表达显著增加(P<0.01)。(3)与WKY-SED组相比,SHR-SED组CaN在肠系膜动脉的蛋白表达显著增加(P<0.01),p-NFATc3的蛋白表达显著减少(P<0.01);与SHR-SED组相比,SHR-EX组CaN的蛋白表达显著减少(P<0.01),p-NFATc3的蛋白表达显著增加(P<0.01)。(4)与WKY-SED组相比,SHR-SED组的AKAP150蛋白表达显著增加(P<0.01);与SHR-SED组相比,SHR-EX组的AKAP150蛋白表达显著减少(P<0.01)。(5)与WKY-SED组相比,SHR-SED组的CaM蛋白表达显著增加(P<0.01);与SHR-SED组相比,SHR-EX组的CaM蛋白表达显著减少(P<0.01);相比WKY-SED组,WKY-EX组CaM的蛋白表达量显著升高(P<0.05)。结论 钙调磷酸酶/活化T细胞核因子信号通路表达上调是高血压引起KV2.1通道功能下降的重要原因,有氧运动可以有效抑制这种作用,这可能是有氧运动缓解高血压及重塑血管功能的机制之一。

    Abstract:

    Aim To investigate the role of calcineurin/nuclear factor of activated T cells (CaN/NFAT) signaling pathway in aerobic exercise-induced increased expression of KV2.1 channel in mesenteric artery vascular smooth muscle cell from spontaneously hypertensive rats (SHR). Methods Male SHR and Wistar-Kyoto rats (WKY), 12 weeks age, were randomly divided into control groups (WKY-SED, SHR-SED), and exercise groups (WKY-EX, SHR-EX). Exercise groups were subjected to a 12-week treadmill training protocol:20 m/min, 60 min/day, 5 d/w. After 12 weeks, heart rate (HR) and blood pressure (BP) was acquired in each group. Immunocytochemistry was used to observe the distribution and changing of KV2.1 and CaN in mesenteric artery (MA). Western blot was applied to examine the expression levels of KV2.1, CaN, NFATc3, p-NFATc3, A-kinase anchoring protein (AKAP150) and calmodulin (CaM) protein in MA. Results (1)After 12 weeks of exercise, HR, systolic blood pressure (SBP)and mean blood pressure (MBP) in SHR-EX group was significantly lower than that in SHR-SED group (P<0.01); SBP in WKY-EX group was lower than that in WKY-SED group (P<0.05). (2) The distribution and protein expression of KV2.1 in SHR-SED group was significantly lower than that in WKY-SED group (P<0.01); Exercise training markedly increased the expression of KV2.1 in SHR-EX group (P<0.01). (3) Compared with the WKY-SED group, the distribution and protein expression of CaN was significantly increased, but the protein expression of p-NFATc3 was significantly lower in SHR-SED group(P<0.01); Exercise training markedly inhibited the distribution and expression of CaN and increased the expression of p-NFATc3 in SHR-EX group (P<0.01). (4) The protein expression of AKAP150 in SHR-SED group was significantly higher than that of WKY-SED group (P<0.01); aerobic exercise obviously decreased the upregulation protein expression of AKAP150 in hypertension(P<0.01). (5) The protein expression of CaM in SHR-SED group was significantly higher than that of WKY-SED group (P<0.01); Compared with the SHR-SED group, the protein expression of CaM was significantly decreased in SHR-EX group (P<0.01); Compared with the WKY-SED group, the protein expression of CaM was significantly increased in WKY-EX group (P<0.05). Conclusion The increased CaN/NFAT signaling pathway may induce the KV2.1 expression downregulation, however, aerobic exercise can effectively inhibit such effects, which may be the mechanism of exercise restoring cardiovascular function.

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李珊珊,柏平,吴迎,李丽,曾凡星,石丽君.钙调磷酸酶/活化T细胞因子信号通路在有氧运动诱导高血压大鼠血管平滑肌细胞KV2.1通道表达上调中的作用[J].中国动脉硬化杂志,2018,26(8):767~773.

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  • 收稿日期:2018-02-09
  • 最后修改日期:2018-03-21
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  • 在线发布日期: 2018-07-17