摘要
Background Treatment with inhaled carbon monoxide （CO） has been shown to ameliorate intestinal injury in experimental animals induced by lipopolysaccharide （LPS） or ischemia-reperfusion. We hypothesized that CO intraperitoneal administration （i.p.） might provide similar protection to inhaled gas. This study aimed to investigate the effects of continuous 2 L/min of 250 ppm CO i.p. on rat intestine injury induced by LPS and to try to develop a more practical means of delivering the gas. Methods A total of 72 male Sprague-Dawley rats were randomly assigned to 4 groups： control group, CO i.p. group, LPS group and LPS＋CO i.p. group. One hour after intravenously received 5 mg/kg LPS, the rats in LPS group and LPS＋CO i.p. group were exposed to room air and 2 L/min of 250 ppm CO i.p., respectively, and the rats of control group and CO i.p. group intravenously received an equal volume of 0.9% NaCI and 1 hour later, were exposed to room air and 2 L/min of 250 ppm CO i.p., respectively. One, 3 and 6 hour of each group after treated with room air or CO i.p., the animals （n=-6 for each time point） were sacrificed and intestinal tissues were collected for determinating the levels of platelet activator factor （PAF） and intercellular adhesion molecule-1 （ICAM-1） with enzyme-lined immunosorbent assays. The maleic dialdehyde （MDA） content and the myeloperoxidase （MPO） activity were determined with a chemical method. The phosphorylated p38 mitogen activated protein kinase （MAPK） expression was assayed with Western blotting and the cell apoptotic rate with flow cytometery. The arterial oxygenation was measured by blood gas analysis, and the pathology determined by light microscope. Results After treatment with 2 L/min of 250 ppm CO i.p., the increase of PAF, ICAM-1, MDA, MPO, and cell apoptotic rate induced by LPS was markedly reduced （P 〈0.05 or 0.01）, and accompanied by ameliorating intestine injury. Western blotting showed that these effects of CO i.p. were mediated by p38 MAPK pathway. There were no significant differences in all observed parameters between control group and CO i.p. group. Conclusion The injury to the intestine via anti-oxidant, anti-inflammation and anti-apoptosis, which may involve the p38 MAPK pathway, was induced by 2 L/min of 250 ppm CO i.p. exerting potent protection against LPS.
Background Treatment with inhaled carbon monoxide （CO） has been shown to ameliorate intestinal injury in experimental animals induced by lipopolysaccharide （LPS） or ischemia-reperfusion. We hypothesized that CO intraperitoneal administration （i.p.） might provide similar protection to inhaled gas. This study aimed to investigate the effects of continuous 2 L/min of 250 ppm CO i.p. on rat intestine injury induced by LPS and to try to develop a more practical means of delivering the gas. Methods A total of 72 male Sprague-Dawley rats were randomly assigned to 4 groups： control group, CO i.p. group, LPS group and LPS＋CO i.p. group. One hour after intravenously received 5 mg/kg LPS, the rats in LPS group and LPS＋CO i.p. group were exposed to room air and 2 L/min of 250 ppm CO i.p., respectively, and the rats of control group and CO i.p. group intravenously received an equal volume of 0.9% NaCI and 1 hour later, were exposed to room air and 2 L/min of 250 ppm CO i.p., respectively. One, 3 and 6 hour of each group after treated with room air or CO i.p., the animals （n=-6 for each time point） were sacrificed and intestinal tissues were collected for determinating the levels of platelet activator factor （PAF） and intercellular adhesion molecule-1 （ICAM-1） with enzyme-lined immunosorbent assays. The maleic dialdehyde （MDA） content and the myeloperoxidase （MPO） activity were determined with a chemical method. The phosphorylated p38 mitogen activated protein kinase （MAPK） expression was assayed with Western blotting and the cell apoptotic rate with flow cytometery. The arterial oxygenation was measured by blood gas analysis, and the pathology determined by light microscope. Results After treatment with 2 L/min of 250 ppm CO i.p., the increase of PAF, ICAM-1, MDA, MPO, and cell apoptotic rate induced by LPS was markedly reduced （P 〈0.05 or 0.01）, and accompanied by ameliorating intestine injury. Western blotting showed that these effects of CO i.p. were mediated by p38 MAPK pathway. There were no significant differences in all observed parameters between control group and CO i.p. group. Conclusion The injury to the intestine via anti-oxidant, anti-inflammation and anti-apoptosis, which may involve the p38 MAPK pathway, was induced by 2 L/min of 250 ppm CO i.p. exerting potent protection against LPS.
基金
This work was supported by the grants from the Natural Science Foundation of Jiangsu Province （No. 98029） and the Scientific Development Foundation of Jiangsu Province （No. 2000409）.
