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中视前核中的脑源性“哇巴因”介导自发性高血压大鼠的钠敏感性高血压。

Brain 'ouabain' in the median preoptic nucleus mediates sodium-sensitive hypertension in spontaneously hypertensive rats.

作者信息

Budzikowski A S, Leenen F H

机构信息

Hypertension Unit, University of Ottawa Heart Institute, Ottawa, Canada.

出版信息

Hypertension. 1997 Feb;29(2):599-605. doi: 10.1161/01.hyp.29.2.599.

DOI:10.1161/01.hyp.29.2.599
PMID:9040445
Abstract

Pressor responses to an acute increase in cerebrospinal fluid sodium and exaggeration of the hypertension and sympathetic hyperreactivity in spontaneously hypertensive rats (SHR) by high sodium diet involve release of brain "ouabain" and subsequent activation of the brain renin-angiotensin system. In the present study, we determined whether release of "ouabain" in the median preoptic nucleus participates in these responses. In conscious Wistar rats, the pressor and heart rate responses to central hypertonic saline (0.3 mol/L NaCl, 3.8 microL/min over 10 minutes) and ouabain (0.6 microgram) were compared after median preoptic nucleus injection of either gamma-globulins or Fab fragments binding ouabain and brain "ouabain" with high affinity. Microinjection of Fab fragments into the median preoptic nucleus abolished the pressor and tachycardic responses to central hypertonic saline and significantly reduced the pressor response to central ouabain. In SHR on high sodium, microinjection of Fab fragments into the median preoptic nucleus significantly decreased baseline blood pressure to a level not different from that in SHR on regular sodium (149 +/- 7 versus 145 +/- 5 mm Hg), whereas the enhanced responses to air stress were not affected. Our results support the concept that blood pressure responses to central hypertonic saline and exaggeration of the hypertension in SHR by high sodium diet depend on release of brain "ouabain" in the median preoptic nucleus.

摘要

脑脊液钠急性升高引起的升压反应,以及高钠饮食使自发性高血压大鼠(SHR)的高血压和交感神经反应性增强,都涉及脑“哇巴因”的释放以及随后脑肾素-血管紧张素系统的激活。在本研究中,我们确定视前正中核中“哇巴因”的释放是否参与了这些反应。在清醒的Wistar大鼠中,在视前正中核注射高亲和力结合哇巴因和脑“哇巴因”的γ球蛋白或Fab片段后,比较对中枢高渗盐水(0.3 mol/L NaCl,10分钟内3.8 μL/分钟)和哇巴因(0.6微克)的升压和心率反应。向视前正中核微量注射Fab片段消除了对中枢高渗盐水的升压和心动过速反应,并显著降低了对中枢哇巴因的升压反应。在高钠饮食的SHR中,向视前正中核微量注射Fab片段可使基线血压显著降低至与正常钠饮食的SHR无差异的水平(149±7对145±5 mmHg),而对空气应激增强的反应未受影响。我们的结果支持这样的概念,即对中枢高渗盐水的血压反应以及高钠饮食使SHR高血压加重,取决于视前正中核中脑“哇巴因”的释放。

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