Department of Anesthesiology, Taipei Veterans General Hospital and National Yang-Ming University, Taipei, Taiwan, ROC.
Intensive Care Med. 2010 Sep;36(9):1571-8. doi: 10.1007/s00134-010-1839-z. Epub 2010 Mar 11.
The pathogenesis of multiple organ dysfunction syndrome (MODS) in septic shock is mainly caused by maldistribution of tissue perfusion and the amplification of inflammatory responses, which may be modulated by beta(2)-adrenoceptor agonists. We evaluated and compared effects of terbutaline on MODS in a cecal ligation and puncture (CLP) model of sepsis.
Prospective controlled animal study in a university laboratory.
Male adult Wistar rats received CLP or sham operation followed by the administration of saline or terbutaline (0.3 mg/kg i.v. at 3 and 9 h after CLP).
At 0, 9 and 18 h after CLP, the changes of hemodynamics, organ function indexes, as well as the plasma interleukin-1beta (IL-1beta) and nitrite/nitrate levels were examined. At 18 h after CLP, animals were killed and their lungs, livers and kidneys were immediately excised to analyze superoxide anion (O(2) (-)) levels and inducible nitric oxide synthase (iNOS) expression. These organs were also evaluated by pathological study. Terbutaline significantly (1) prevented delayed hypotension and reduced hepatic and renal dysfunction, (2) diminished plasma IL-1beta and nitrite/nitrate, lung iNOS expression, tissue O(2) (-) level and the infiltration of neutrophils in the lung and the liver, and (3) improved the 18-h survival rate.
Terbutaline may be developed as an alternative treatment for severe sepsis-induced MODS. The protective effect of terbutaline seems to be through inhibition of proinflammatory mediators and attenuation of oxidant production.
感染性休克多器官功能障碍综合征(MODS)的发病机制主要是由于组织灌注分布不良和炎症反应的放大,这可能是由β(2)-肾上腺素能受体激动剂调节的。我们评估并比较了特布他林对盲肠结扎和穿刺(CLP)感染模型中 MODS 的影响。
大学实验室的前瞻性对照动物研究。
雄性成年 Wistar 大鼠接受 CLP 或假手术,然后给予生理盐水或特布他林(CLP 后 3 和 9 小时静脉注射 0.3mg/kg)。
CLP 后 0、9 和 18 小时,检查血流动力学变化、器官功能指标以及血浆白细胞介素-1β(IL-1β)和亚硝酸盐/硝酸盐水平。CLP 后 18 小时,处死动物,立即取出其肺、肝和肾,分析超氧阴离子(O2(-))水平和诱导型一氧化氮合酶(iNOS)表达。通过病理研究还评估了这些器官。特布他林显著:(1)预防迟发性低血压,减少肝肾功能障碍;(2)降低血浆 IL-1β和亚硝酸盐/硝酸盐、肺 iNOS 表达、组织 O2(-)水平和肺及肝内中性粒细胞浸润;(3)提高 18 小时存活率。
特布他林可作为治疗严重感染性休克引起的 MODS 的一种替代方法。特布他林的保护作用似乎是通过抑制促炎介质和减少氧化剂的产生。