Intensive Care Unit, Nagasaki University Hospital, 1-7-1 Sakamoto, Nagasaki 852-8501, Japan.
Anesth Analg. 2010 Jan 1;110(1):141-7. doi: 10.1213/ANE.0b013e3181c4ee6c. Epub 2009 Nov 21.
Pharmacological blockade of the renin-angiotensin system is thought to maintain gut perfusion during circulatory stress and thereby avoid later failure of distant organs. In this controlled experimental study, we investigated the effects of carperitide, a synthetic atrial natriuretic peptide that inhibits the renin-angiotensin system, on the systemic and splanchnic circulation during fluid-resuscitated endotoxemia in pigs.
Sixteen domestic pigs of both sexes were randomly divided into 2 groups. The pigs were anesthetized and their lungs ventilated before receiving either saline (Group A: n = 8) or carperitide (Group B: n = 8). After a baseline measurement was taken, the pigs from both groups received a continuous infusion (1.7 microg x kg(-1) x h(-1)) of endotoxin for 240 min. Group B received a continuous infusion of carperitide (0.05 microg x kg(-1) x min(-1)) starting 30 min before the endotoxin infusion and lasting until the end of the study, whereas Group A received the same volume of saline. Fluid resuscitation was titrated to maintain pulmonary artery wedge pressure between 10 and 12 mm Hg. Systemic and regional hemodynamics, oxygenation variables, and the arterial-to-intestinal PCO(2) gap were measured at baseline and after endotoxin infusion for 240 min. The primary end points were cardiac index, superior mesenteric artery flow index, and PCO(2) gap at the end of this study (T240).
Cardiac index and superior mesenteric artery flow index in Group B were significantly higher than those in Group A at T240 (83 +/- 15 vs 135 +/- 23 mL x kg(-1) x min(-1), P < 0.001; 2.6 +/- 1.4 vs 7.9 +/- 4.8, P = 0.01), respectively. Carperitide administration resulted in a significantly better maintenance of intestinal mucosal perfusion assessed by the PCO(2) gap at T240 (33.0 +/- 14.5 vs 11.6 +/- 10.0 mm Hg, P = 0.004). The PaO(2)/FIO(2) ratio in Group B was significantly greater than that in Group A from T60 to T240.
In this porcine fluid-resuscitated endotoxemia model, a low dose of carperitide administered before endotoxemia maintained systemic and splanchnic circulation, and prevented the deterioration of oxygenation. Atrial natriuretic peptide infusion is a potentially beneficial therapy with respect to systemic and splanchnic circulation as well as the respiratory system during sepsis.
人们认为,药理学阻断肾素-血管紧张素系统可以在循环压力期间维持肠道灌注,从而避免远处器官的后期衰竭。在这项对照实验研究中,我们研究了在心内肽,一种抑制肾素-血管紧张素系统的合成心钠肽,对接受液体复苏的内毒素血症猪的全身和内脏循环的影响。
16 只雄性和雌性家猪被随机分为 2 组。在接受盐水(A 组:n = 8)或心内肽(B 组:n = 8)之前,猪被麻醉并进行肺部通气。在进行基线测量后,两组猪均接受内毒素持续输注(1.7 microg x kg(-1) x h(-1))240 分钟。B 组在接受内毒素输注前 30 分钟开始持续输注心内肽(0.05 microg x kg(-1) x min(-1)),持续至研究结束,而 A 组接受相同体积的生理盐水。液体复苏滴定以维持肺动脉楔压在 10 至 12 毫米汞柱之间。在基线和内毒素输注 240 分钟后测量全身和区域血流动力学、氧合变量和动脉-肠道 PCO(2)间隙。主要终点是研究结束时(T240)的心指数、肠系膜上动脉血流指数和 PCO(2)间隙。
B 组的心指数和肠系膜上动脉血流指数在 T240 时明显高于 A 组(83 +/- 15 与 135 +/- 23 mL x kg(-1) x min(-1),P < 0.001;2.6 +/- 1.4 与 7.9 +/- 4.8,P = 0.01)。心内肽给药可显著更好地维持肠道黏膜灌注,T240 时 PCO(2)间隙(33.0 +/- 14.5 与 11.6 +/- 10.0 mm Hg,P = 0.004)。B 组的 PaO(2)/FIO(2)比值从 T60 到 T240 明显大于 A 组。
在这种接受液体复苏的内毒素血症猪模型中,在内毒素血症前给予低剂量的心内肽可维持全身和内脏循环,并防止氧合恶化。心钠肽输注可能是一种有益的治疗方法,可改善脓毒症期间的全身和内脏循环以及呼吸系统。