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Hypervolemia induces and potentiates lung damage after recruitment maneuver in a model of sepsis-induced acute lung injury

机译:在脓毒症诱发的急性肺损伤模型中,募集后高血容量诱导并增强肺损伤

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IntroductionRecruitment maneuvers (RMs) seem to be more effective in extrapulmonary acute lung injury (ALI), caused mainly by sepsis, than in pulmonary ALI. Nevertheless, the maintenance of adequate volemic status is particularly challenging in sepsis. Since the interaction between volemic status and RMs is not well established, we investigated the effects of RMs on lung and distal organs in the presence of hypovolemia, normovolemia, and hypervolemia in a model of extrapulmonary lung injury induced by sepsis.MethodsALI was induced by cecal ligation and puncture surgery in 66 Wistar rats. After 48 h, animals were anesthetized, mechanically ventilated and randomly assigned to 3 volemic status (n = 22/group): 1) hypovolemia induced by blood drainage at mean arterial pressure (MAP)≈70 mmHg; 2) normovolemia (MAP≈100 mmHg), and 3) hypervolemia with colloid administration to achieve a MAP≈130 mmHg. In each group, animals were further randomized to be recruited (CPAP = 40 cm H2O for 40 s) or not (NR) (n = 11/group), followed by 1 h of protective mechanical ventilation. Echocardiography, arterial blood gases, static lung elastance (Est,L), histology (light and electron microscopy), lung wet-to-dry (W/D) ratio, interleukin (IL)-6, IL-1β, caspase-3, type III procollagen (PCIII), intercellular adhesion molecule-1 (ICAM-1), and vascular cell adhesion molecule-1 (VCAM-1) mRNA expressions in lung tissue, as well as lung and distal organ epithelial cell apoptosis were analyzed.ResultsWe observed that: 1) hypervolemia increased lung W/D ratio with impairment of oxygenation and Est,L, and was associated with alveolar and endothelial cell damage and increased IL-6, VCAM-1, and ICAM-1 mRNA expressions; and 2) RM reduced alveolar collapse independent of volemic status. In hypervolemic animals, RM improved oxygenation above the levels observed with the use of positive-end expiratory pressure (PEEP), but increased lung injury and led to higher inflammatory and fibrogenetic responses.ConclusionsVolemic status should be taken into account during RMs, since in this sepsis-induced ALI model hypervolemia promoted and potentiated lung injury compared to hypo- and normovolemia.
机译:简介招募策略(RMs)在主要由败血症引起的肺外急性肺损伤(ALI)中似乎比在肺ALI中更有效。然而,在败血症中维持适当的血栓状态尤其具有挑战性。由于血流状态与RMs之间的相互作用尚未完全确立,因此我们在败血症引起的肺外肺损伤模型中研究了RMs在低血容量,正常血容量和高血容量存在下对肺和远端器官的影响。 66只Wistar大鼠的结扎和穿刺手术。 48小时后,对动物进行麻醉,机械通气,并随机分为3种血流状态(n = 22 /组):1)在平均动脉压(MAP)≈70 mmHg的情况下通过引流引起的血容量不足。 2)正常血容量(MAP≈100mmHg),3)胶体给药引起的血容量过高,以达到MAP≈130mmHg。在每组中,进一步将动物随机分组(CPAP = 40 cm H2O 40 s)或否(NR)(n = 11 /组),然后进行1 h的保护性机械通气。超声心动图,动脉血气,静态肺弹性(Est,L),组织学(光学和电子显微镜),肺干湿比(W / D),白介素(IL)-6,IL-1β,胱天蛋白酶3 ,III型原胶原(PCIII),细胞间粘附分子1(ICAM-1)和血管细胞粘附分子1(VCAM-1)mRNA在肺组织中的表达以及肺和远端器官上皮细胞的凋亡进行了分析。结果我们观察到:1)高血容量增加肺W / D比,损害氧合作用和Est,L,并与肺泡和内皮细胞损伤以及IL-6,VCAM-1和ICAM-1 mRNA表达增加有关; 2)RM减少了肺泡塌陷,而与血栓状态无关。在高血容量动物中,RM改善了超过使用正向呼气压力(PEEP)所观察到的水平的氧合作用,但增加了肺损伤并导致更高的炎症和纤维化反应。结论在RM期间应考虑血栓状态,因为在这种情况下与低血脂和高血脂血症相比,脓毒症诱导的ALI模型血容量过多可促进和增强肺损伤。

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