Department of Anesthesia and Critical Care, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Crit Care Med. 2010 May;38(5):1335-42. doi: 10.1097/CCM.0b013e3181d99e67.
To determine the role of toll-like receptor 2 in cardiac dysfunction during polymicrobial sepsis.
Controlled animal study.
University hospital research laboratory.
Male C57BL/6, wild-type, toll-like receptor 2-/-.
Polymicrobial peritonitis, a clinically relevant model of sepsis, was generated by cecum ligation and puncture. Wild-type and toll-like receptor 2-/- mice were divided into sham and cecum ligation and puncture groups. The sham animals underwent laparotomy but without cecum ligation and puncture. Twenty-four hours after surgeries, the cardiac function was assessed by serial echocardiography in vivo, a pressure transducer catheter was inserted into the left ventricles of isolated hearts (Langendorff model), and in vitro measurement of Ca2+ transients and sarcomere shortening in adult cardiomyocytes were isolated from the sham and septic animals. In addition, myocardial and serum cytokines, blood white blood cell counts, peritoneal neutrophil recruitment, chemokine receptor expression, and survival rates were examined.
Compared to septic wild-type mice, toll-like receptor 2-/- mice had markedly improved cardiac function during sepsis, as demonstrated by in vivo tissue Doppler imaging, better-preserved left ventricle function in isolated heart, and improved sarcomere shortening measured in single cardiomyocytes. There was also a significant survival benefit in toll-like receptor 2-/- mice compared to wild-type mice. These favorable outcomes in toll-like receptor 2-/- mice were associated with attenuated cardiodepressant cytokine levels in the myocardium and serum and enhanced neutrophil migratory function.
These studies suggest that toll-like receptor 2 signaling plays a critical role in mediating cardiomyopathy, deleterious myocardial and systemic inflammation, and high mortality during polymicrobial sepsis.
确定 Toll 样受体 2 在多微生物脓毒症导致的心功能障碍中的作用。
对照动物研究。
大学医院研究实验室。
雄性 C57BL/6,野生型,Toll 样受体 2-/-。
盲肠结扎穿刺术建立多微生物腹膜炎,这是一种与脓毒症相关的临床模型。野生型和 Toll 样受体 2-/-小鼠分为假手术组和盲肠结扎穿刺术组。假手术组仅行剖腹术但不结扎和穿刺盲肠。手术后 24 小时,通过活体连续超声心动图评估心功能,将压力传感器导管插入左心室(Langendorff 模型),并从假手术和脓毒症动物中分离出成年心肌细胞,检测 Ca2+ 瞬变和肌节缩短的体外测量。此外,还检测了心肌和血清细胞因子、白细胞计数、腹膜中性粒细胞募集、趋化因子受体表达和存活率。
与脓毒症野生型小鼠相比,Toll 样受体 2-/-小鼠在脓毒症期间心功能明显改善,表现为组织多普勒成像显示的心脏组织多普勒成像、离体心脏左心室功能更好、以及在单个心肌细胞中测量的肌节缩短得到改善。Toll 样受体 2-/-小鼠的存活率也明显优于野生型小鼠。Toll 样受体 2-/-小鼠的这些有利结果与心肌和血清中抑制心肌细胞的细胞因子水平降低以及中性粒细胞迁移功能增强有关。
这些研究表明,Toll 样受体 2 信号在介导多微生物脓毒症中心肌病、有害的心肌和全身炎症以及高死亡率方面发挥着关键作用。