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脑氧化应激引起的交感兴奋介导盐诱导的慢性肾脏病中的动脉血压升高。

Sympathoexcitation by brain oxidative stress mediates arterial pressure elevation in salt-induced chronic kidney disease.

机构信息

Department of Nephrology and Endocrinology, Faculty of Medicine, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655, Japan.

出版信息

Hypertension. 2012 Jan;59(1):105-12. doi: 10.1161/HYPERTENSIONAHA.111.182923. Epub 2011 Nov 14.

Abstract

Hypertension is very prevalent in chronic kidney disease and critical for its prognosis. Sympathoexcitation and oxidative stress have been demonstrated to be involved in chronic kidney disease. We have shown previously that sympathoexcitation by brain oxidative stress mediates arterial pressure elevation in the salt-sensitive hypertension model, Dahl salt-sensitive rats. Thus, we investigated whether sympathoexcitation by excessive brain oxidative stress could contribute to arterial pressure elevation in salt-induced chronic kidney disease model rats. Young (3-week-old) male Sprague-Dawley rats were randomly assigned to a uninephrectomy or sham operation and then subjected to either a normal salt (0.5%) or high-salt (8.0%) diet for 4 weeks. The young salt-loaded uninephrectomized rats exhibited sympathoexcitation, hypertension, and renal injury, proteinuria and global glomerulosclerosis together with tubulointerstitial damage. Under urethane anesthesia and artificial ventilation, renal sympathetic nerve activity, arterial pressure, and heart rate decreased to a greater degree in the salt-loaded uninephrectomized rats than in the nonsalt-loaded uninephrectomized rats and the salt-loaded or nonsalt-loaded sham-operated rats, when Tempol, a membrane-permeable superoxide dismutase mimetic, was infused acutely into the lateral cerebral ventricle. Oxidative stress in the hypothalamus, measured by lucigenin chemiluminescence, was also significantly greater. Furthermore, in the salt-loaded uninephrectomized rats, antioxidant treatment with chronic intracerebroventricular Tempol decreased sympathetic nerve activity and arterial pressure, which, in turn, led to a decrease in renal damage. Similar effects were elicited by treatment with oral moxonidine, the central sympatholytic agent. In conclusion, sympathoexcitation by brain oxidative stress may mediate arterial pressure elevation in salt-induced chronic kidney disease.

摘要

高血压在慢性肾脏病中非常普遍,对其预后至关重要。交感神经兴奋和氧化应激已被证明与慢性肾脏病有关。我们之前已经表明,脑氧化应激引起的交感神经兴奋介导了盐敏感高血压模型(Dahl 盐敏感大鼠)中的动脉血压升高。因此,我们研究了过量脑氧化应激引起的交感神经兴奋是否会导致盐诱导的慢性肾脏病模型大鼠的动脉血压升高。年轻(3 周龄)雄性 Sprague-Dawley 大鼠被随机分为单侧肾切除术或假手术组,然后给予正常盐(0.5%)或高盐(8.0%)饮食 4 周。年轻的盐负荷单侧肾切除大鼠表现出交感神经兴奋、高血压和肾脏损伤,蛋白尿和肾小球整体硬化症以及肾小管间质损伤。在乌拉坦麻醉和人工通气下,当 Tempol(一种膜通透超氧化物歧化酶模拟物)急性输注到侧脑室时,盐负荷单侧肾切除大鼠的肾交感神经活性、动脉压和心率下降幅度大于非盐负荷单侧肾切除大鼠以及盐负荷或非盐负荷假手术大鼠。下丘脑的氧化应激,通过荧光素化学发光测量,也显著增加。此外,在盐负荷单侧肾切除大鼠中,慢性脑室内 Tempol 的抗氧化治疗可降低交感神经活性和动脉压,从而导致肾脏损伤减少。口服莫索尼定(中枢交感神经抑制剂)也可产生类似的效果。总之,脑氧化应激引起的交感神经兴奋可能介导盐诱导的慢性肾脏病中的动脉血压升高。

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