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首页> 外文期刊>American Journal of Physiology >Protective effect of renal denervation on normotensive endotoxemia-induced acute renal failure in mice.
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Protective effect of renal denervation on normotensive endotoxemia-induced acute renal failure in mice.

机译:肾神经支配对正常血压内毒素血症引起的小鼠急性肾衰竭的保护作用。

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摘要

Acute renal failure (ARF) contributes substantially to the high morbidity and mortality observed during endotoxemia. We hypothesized that selective blockade of the renal nerves would be protective against ARF during the early (16 h) stage of endotoxemia [5 mg lipopolysaccharide (LPS)/kg ip in mice]. At 16 h after LPS, there was no change in mean arterial pressure, but plasma epinephrine (4,604 +/- 719 vs. 490 +/- 152 pg/ml, P < 0.001), norepinephrine (2,176 +/- 306 vs. 1,224 +/- 218 pg/ml, P < 0.05), and plasma renin activity (40 +/- 5 vs. 27 +/- 2 ng x ml(-1) x h(-1), P < 0.05) were higher in the LPS-treated vs. control mice. The high plasma renin activity level decreased to the control level with renal denervation in endotoxemic mice. After intravenous injection of phentolamine (200 microg/kg), the decrement in mean arterial pressure was significantly greater in LPS-treated vs. control mice (19.4 +/- 3.5 vs. 8.1 +/- 1.5 mmHg, P < 0.01). Sixteen hours after LPS administration, there were significant decreases in glomerular filtration rate (52 +/- 18 vs. 212 +/- 23 microl/min, P < 0.01) and renal blood flow (0.58 +/- 0.08 vs. 0.85 +/- 0.06 ml/min, P < 0.01) in sham-operated mice. The decrement in glomerular filtration rate during endotoxemia was significantly attenuated in mice with denervated kidneys (32 vs. 79%). Moreover, there was no change in renal blood flow during endotoxemia in mice with renal denervation. The present results therefore demonstrate a protective role of renal denervation during normotensive endotoxemia-related ARF in mice, an effect that may be, at least in part, due to a diminished activation of the renin-angiotensin system.
机译:急性肾衰竭(ARF)在内毒素血症期间观察到的高发病率和高死亡率中起着重要作用。我们假设在内毒素血症的早期(16 h)阶段,选择性阻断肾神经可以抵抗ARF [5 mg脂多糖(LPS)/ kg ip小鼠]。 LPS后16小时,平均动脉压没有变化,但血浆肾上腺素(4,604 +/- 719 vs. 490 +/- 152 pg / ml,P <0.001),去甲肾上腺素(2,176 +/- 306 vs. 1,224) +/- 218 pg / ml,P <0.05)和血浆肾素活性(40 +/- 5 vs. 27 +/- 2 ng x ml(-1)xh(-1),P <0.05)较高经LPS处理的小鼠与对照组的小鼠。内毒素血症小鼠的肾脏去神经支配后,血浆高肾素活性水平降低至对照水平。静脉注射苯妥拉明(200微克/千克)后,经LPS处理的小鼠的平均动脉压降幅明显大于对照小鼠(19.4 +/- 3.5 vs. 8.1 +/- 1.5 mmHg,P <0.01)。给予LPS后16小时,肾小球滤过率(52 +/- 18 vs. 212 +/- 23 microl / min,P <0.01)和肾血流量(0.58 +/- 0.08 vs. 0.85 + / -在假手术小鼠中为0.06 ml / min,P <0.01)。肾无神经的小鼠内毒素血症期间肾小球滤过率的降低明显减弱(32%vs. 79%)。此外,内毒素血症小鼠肾脏去神经支配期间肾血流量没有变化。因此,本发明结果证明了在小鼠血压正常性内毒素血症相关的ARF期间肾神经支配的保护作用,这种作用可能至少部分是由于肾素-血管紧张素系统的激活减少。

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