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上皮钠通道阻断对大鼠近髓传入小动脉肌源性反应的影响。

Effect of epithelial sodium channel blockade on the myogenic response of rat juxtamedullary afferent arterioles.

作者信息

Guan Zhengrong, Pollock Jennifer S, Cook Anthony K, Hobbs Janet L, Inscho Edward W

机构信息

Department of Physiology, Medical College of Georgia, Augusta, GA 30912, USA.

出版信息

Hypertension. 2009 Nov;54(5):1062-9. doi: 10.1161/HYPERTENSIONAHA.109.137992. Epub 2009 Aug 31.

Abstract

The mechanotransduction mechanism underlying the myogenic response is poorly understood, but evidence implicates participation of epithelial sodium channel (ENaC)-like proteins. Therefore, the role of ENaC on the afferent arteriolar myogenic response was investigated in vitro using the blood-perfused juxtamedullary nephron technique. Papillectomy was used to isolate myogenic influences by eliminating tubuloglomerular feedback signals. Autoregulatory responses were assessed by manipulating perfusion pressure in 30-mm Hg steps. Under control conditions, arteriolar diameter increased by 15% from 13.0+/-1.3 to 14.7+/-1.2 microm (P<0.05) after reducing perfusion pressure from 100 to 70 mm Hg. Diameter decreased to 11.3+/-1.1 and 10.6+/-1.0 microm after increasing pressure to 130 and 160 mm Hg (88+/-1 and 81+/-2% of control diameter, P<0.05), respectively. Pressure-mediated autoregulatory responses were significantly inhibited by superfusion of 10 micromol/L amiloride (102+/-2, 97+/-4, and 94+/-3% of control diameter), or 10 micromol/L benzamil (106+/-5, 100+/-3, and 103+/-3% of control diameter), and when perfusing with blood containing 5 micromol/L amiloride (106+/-2, 97+/-4, and 97+/-4% of control diameter). Vasoconstrictor responses to 55 mmol/L KCl were preserved as diameters decreased by 67+/-4, 55+/-8, and 60+/-4% in afferent arterioles superfused with amiloride or benzamil, and perfused with amiloride, respectively. These responses were similar to responses obtained from control afferent arterioles (64+/-6%, P>0.05). Immunofluorescence revealed expression of the alpha, beta, and gamma subunits of ENaC in freshly isolated preglomerular microvascular smooth muscle cells. These results demonstrate that selective ENaC inhibitors attenuate afferent arteriolar myogenic responses and suggest that ENaC may function as mechanosensitive ion channels initiating pressure-dependent myogenic responses in rat juxtamedullary afferent arterioles.

摘要

肌源性反应背后的机械转导机制目前了解甚少,但有证据表明上皮钠通道(ENaC)样蛋白参与其中。因此,我们使用血液灌注的近髓肾单位技术在体外研究了ENaC在传入小动脉肌源性反应中的作用。通过切除乳头来消除肾小管-肾小球反馈信号,以分离肌源性影响。通过以30mmHg的步长操纵灌注压力来评估自动调节反应。在对照条件下,将灌注压力从100mmHg降至70mmHg后,小动脉直径从13.0±1.3微米增加到14.7±1.2微米,增幅为15%(P<0.05)。将压力分别增加到130mmHg和160mmHg后,直径分别降至11.3±1.1微米和10.6±1.0微米(分别为对照直径的88±1%和81±2%,P<0.05)。10μmol/L的氨氯吡脒(对照直径的102±2%、97±4%和94±3%)或10μmol/L的苯甲米(对照直径的106±5%、100±3%和103±3%)的超灌注,以及用含5μmol/L氨氯吡脒的血液灌注时,压力介导的自动调节反应均受到显著抑制。对55mmol/L氯化钾的血管收缩反应得以保留,在分别用氨氯吡脒或苯甲米进行超灌注以及用氨氯吡脒灌注的传入小动脉中,直径分别下降了67±4%、55±8%和60±4%。这些反应与对照传入小动脉的反应相似(64±6%,P>0.05)。免疫荧光显示,在新鲜分离的球前微血管平滑肌细胞中存在ENaC的α、β和γ亚基的表达。这些结果表明,选择性ENaC抑制剂可减弱传入小动脉的肌源性反应,并提示ENaC可能作为机械敏感离子通道,在大鼠近髓传入小动脉中引发压力依赖性肌源性反应。

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