Madorin W S, Cepinskas G, Kvietys P R
Vascular Biology Program, Lawson Health Research Institute, London, ON, Canada.
Crit Care Med. 2001 Sep;29(9):1774-9. doi: 10.1097/00003246-200109000-00020.
Peritonitis induced by cecal ligation and perforation results in inflammation and dysfunction of the rat myocardium, an organ remote from the locus of infection. This peritonitis-induced pathology can be prevented by pretreating these animals with lipopolysaccharide before cecal ligation and perforation. In the present study, we assessed a) whether cardiomyocytes obtained from rats subjected to cecal ligation and perforation could induce polymorphonuclear leukocyte transendothelial migration, b) whether these cardiomyocytes could activate endothelial cells (increased proadhesive phenotype), and c) whether these responses could be attenuated by lipopolysaccharide pretreatment.
Prospective animal study.
Experimental animal laboratory.
Male Sprague Dawley rats.
Lipopolysaccharide pretreated and nonpretreated rats were subjected to cecal ligation and perforation or to laparotomy. Myocytes were isolated 6 hrs after surgery and used for in vitro experiments.
Myocytes isolated from cecal ligation and perforation rats promoted migration of polymorphonuclear leukocytes across a rat endothelial cell monolayer, an effect prevented by platelet activating factor receptor antagonists. Myocytes isolated from these animals also increased surface level expression of intercellular adhesion molecule-1 on rat endothelial cells, an effect also prevented by platelet activating factor receptor antagonists. Myocytes isolated from rats pretreated with lipopolysaccharide and then subjected to cecal ligation and perforation did not a) promote polymorphonuclear leukocyte transendothelial migration or b) increase intercellular adhesion molecule-1 surface expression on endothelial cells.
Our findings indicate that induction of peritonitis results in a systemic response that induces cardiac myocytes to become proinflammatory (i.e., these myocytes produce chemotactic factors and activate endothelial cells). This effect of cecal ligation and perforation is abrogated by pretreating animals with lipopolysaccharide before induction of peritonitis.
盲肠结扎穿孔诱导的腹膜炎会导致大鼠心肌发生炎症和功能障碍,心肌是远离感染部位的器官。在盲肠结扎穿孔前用脂多糖预处理这些动物可预防这种腹膜炎诱导的病理变化。在本研究中,我们评估了:a)从经历盲肠结扎穿孔的大鼠获得的心肌细胞是否能诱导多形核白细胞跨内皮迁移;b)这些心肌细胞是否能激活内皮细胞(增加促黏附表型);c)脂多糖预处理是否能减弱这些反应。
前瞻性动物研究。
实验动物实验室。
雄性Sprague Dawley大鼠。
脂多糖预处理和未预处理的大鼠接受盲肠结扎穿孔或剖腹手术。术后6小时分离心肌细胞并用于体外实验。
从盲肠结扎穿孔大鼠分离的心肌细胞促进多形核白细胞穿过大鼠内皮细胞单层迁移,血小板活化因子受体拮抗剂可阻止这种作用。从这些动物分离的心肌细胞还增加了大鼠内皮细胞上细胞间黏附分子-1的表面水平表达,血小板活化因子受体拮抗剂也可阻止这种作用。从经脂多糖预处理然后进行盲肠结扎穿孔的大鼠分离的心肌细胞,既不a)促进多形核白细胞跨内皮迁移,也不b)增加内皮细胞上细胞间黏附分子-1的表面表达。
我们的研究结果表明,腹膜炎的诱导会导致一种全身反应,使心肌细胞变得促炎(即这些心肌细胞产生趋化因子并激活内皮细胞)。在诱导腹膜炎前用脂多糖预处理动物可消除盲肠结扎穿孔的这种作用。