1Florey Institute of Neuroscience and Mental Health, University of Melbourne, VIC, Australia. 2Department of Intensive Care, Austin Health, Heidelberg, VIC, Australia. 3Department of Anaesthesia and Intensive Care, AO Melegnano, PO Uboldo, Cernusco sul Naviglio, Italy. 4Australian and New Zealand Intensive Care Research Centre, Monash University, Melbourne, VIC, Australia. 5Department of Medicine, University of Melbourne, Austin Health, Heidelberg, VIC, Australia.
Crit Care Med. 2014 Jun;42(6):e401-9. doi: 10.1097/CCM.0000000000000302.
To determine the influence of the renal sympathetic nerves on the pathogenesis of septic acute kidney injury.
Interventional control study to determine the effects of renal denervation in ovine hyperdynamic sepsis.
Research Institute.
Twenty-four adult Merino ewes.
The effects of infusion of angiotensin II and norepinephrine and induction of hyperdynamic sepsis by administration of live Escherichia coli were examined in control sheep and in sheep at 2 weeks after bilateral renal denervation (n = 10/group).
Systemic hemodynamics and renal function were measured in conscious sheep instrumented with flow probes on the pulmonary and renal arteries. Angiotensin II, but not norepinephrine, had a greater pressor effect in denervated animals. Sepsis increased cardiac output by 60%, renal blood flow by 35%, and arterial lactate by approximately four-fold. The denervated compared with the control group had a greater degree of hypotension during sepsis (68 vs 81 mm Hg; p = 0.003) and a reduction in the early polyuric response (from 496 to 160 mL at 2-8 hr of sepsis; p < 0.001). Creatinine clearance decreased similarly in both groups.
In experimental hyperdynamic sepsis, renal denervation was associated with greater hypotension and a loss of the initial diuresis, but no significant change in creatinine clearance. In sepsis, the renal nerves help support arterial pressure and determine the initial diuretic response, but septic acute kidney injury developed similarly in the innervated and denervated groups.
确定肾交感神经对脓毒症急性肾损伤发病机制的影响。
干预对照研究,以确定去肾神经支配对绵羊高动力性脓毒症的影响。
研究所。
24 只成年美利奴羊。
在对照组和双侧肾去神经支配 2 周后的绵羊中,观察血管紧张素 II 和去甲肾上腺素输注以及给予活大肠杆菌诱导高动力性脓毒症的影响(每组 n = 10)。
用肺动脉和肾动脉上的流量探头对清醒绵羊进行了全身血流动力学和肾功能测量。血管紧张素 II 而不是去甲肾上腺素对去神经支配的动物有更大的升压作用。脓毒症使心输出量增加 60%,肾血流量增加 35%,动脉乳酸增加约四倍。与对照组相比,脓毒症期间去神经组的低血压程度更大(68 对 81mmHg;p = 0.003),并且早期多尿反应减少(从脓毒症 2-8 小时的 496 降至 160mL;p < 0.001)。两组肌酐清除率均相似下降。
在实验性高动力性脓毒症中,肾去神经支配与更大程度的低血压和初始利尿反应丧失相关,但肌酐清除率无明显变化。在脓毒症中,肾神经有助于维持动脉压并决定初始利尿反应,但有神经支配和去神经支配的两组均发生类似的脓毒症急性肾损伤。