Department of Anesthesiology, Investigational Intensive Care Unit, The University of Texas Medical Branch and Shriners Hospitals for Children, Galveston, TX, USA; Department of Anesthesiology, Intensive Care and Pain Medicine, University of Muenster, Muenster, Germany.
Burns. 2013 Dec;39(8):1565-70. doi: 10.1016/j.burns.2013.04.019. Epub 2013 Jun 13.
Previous studies demonstrated beneficial effects of early neuronal nitric oxide synthase (nNOS) and subsequent inducible NOS (iNOS) inhibition on the development of multiple organ dysfunctions in septic sheep. However, the effects of NOS inhibition on regional blood flow remained undetermined. The current study was conducted to assess the effects of combined NOS inhibition on blood flow to various organs in an ovine sepsis model.
Eighteen adult, female sheep were randomly allocated to the following groups: (1) sham-injured, non-treated group, (2) injured (smoke inhalation and instillation of Pseudomonas aeruginosa into the lungs), non-treated group (control), and (3) injured, treated group (specific nNOS inhibition from 1 h to 12 h and iNOS inhibition from 12 h to 24 h post-injury). Fluorescent microspheres were injected at baseline and various time points post-injury. At the end of the 24-h experimental period, tissue from various organs was harvested.
Blood flow to the ileum was significantly increased in the control group from 12 h to 24 h versus sham (P < 0.05). This increase was attenuated in the treatment group (P < 0.05). In contrast, blood flow to the pancreas was significantly increased in the treatment group after 12 h and 24 h versus both sham and control (P < 0.05). Blood flow to the spleen was significantly lower after 24h in the control group versus sham and treatment (P < 0.05 both).
Combined NOS inhibition significantly influenced the pathologically altered organ perfusion during ovine sepsis. However, this treatment strategy showed heterogeneous effects on organ perfusion, perhaps dependent on the sepsis-related degree of NO production and ensuing changes in regional flow.
先前的研究表明,早期神经元型一氧化氮合酶(nNOS)和随后的诱导型一氧化氮合酶(iNOS)抑制对脓毒症绵羊多器官功能障碍的发展有有益影响。然而,NOS 抑制对局部血流的影响仍不确定。本研究旨在评估联合 NOS 抑制对脓毒症羊模型中各种器官血流的影响。
18 只成年雌性绵羊被随机分为以下三组:(1)假损伤、未治疗组,(2)损伤(吸入烟雾和向肺部注入铜绿假单胞菌)、未治疗组(对照组),和(3)损伤、治疗组(伤后 1 至 12 小时特异性 nNOS 抑制,伤后 12 至 24 小时 iNOS 抑制)。在基线和损伤后不同时间点注射荧光微球。在 24 小时实验期结束时,从各种器官中采集组织。
与假损伤组相比,对照组的回肠血流在 12 至 24 小时之间显著增加(P < 0.05)。在治疗组中,这种增加被减弱(P < 0.05)。相反,与假损伤组和对照组相比,治疗组的胰腺血流在 12 小时和 24 小时后均显著增加(P < 0.05)。与假损伤组和治疗组相比,对照组的脾血流在 24 小时后显著降低(P < 0.05)。
联合 NOS 抑制显著影响脓毒症羊的病理性改变的器官灌注。然而,这种治疗策略对器官灌注的影响具有异质性,这可能取决于与脓毒症相关的 NO 产生程度和随后的区域血流变化。