15 research outputs found

    Mechanism of myocardial protection by pressure-volume unloading involves stretch-induced pathophysiology

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    Gadolinium decreases inflammation related to myocardial ischemia and reperfusion injury

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    <p>Abstract</p> <p>Background</p> <p>The lanthanide cation, gadolinium (GdCl<sub>3</sub>) protects the myocardium against infarction following ischemia and reperfusion. Neutrophils and macrophages are the main leukocytes responsible for infarct expansion after reperfusion. GdCl<sub>3 </sub>interferes with macrophage and neutrophil function in the liver by decreasing macrophage secretion of inflammatory cytokines and neutrophil infiltration. We hypothesized that GdCl<sub>3 </sub>protects against ischemia and reperfusion injury by decreasing inflammation. We determined the impact of GdCl<sub>3 </sub>treatment for reperfusion injury on 1) circulating monoctye and neutrophil counts, 2) secretion of inflammatory cytokines, and 3) influx of monocytes and neutrophils into the myocardium.</p> <p>Methods</p> <p>Rats (n = 3-6/gp) were treated with saline or GdCl<sub>3 </sub>(20 μmol/kg) 15 min prior to a 30 min period of regional ischemia and 120 min reperfusion. Sham rats were not subject to ischemia. Blood was collected either after 30 min ischemia or 120 min reperfusion and hearts were harvested at 120 min reperfusion for tissue analysis. Blood was analyzed for leukocytes counts and cytokines. Tissue was analyzed for cytokines and markers of neutrophil and monocyte infiltration by measuring myeloperoxidase (MPO) and α-naphthyl acetate esterase (ANAE).</p> <p>Results</p> <p>GdCl<sub>3 </sub>did not affect the number of circulating neutrophils prior to ischemia. Two hours reperfusion resulted in a 2- and 3- fold increase in circulating monocytes and neutrophils, respectively. GdCl<sub>3 </sub>decreased the number of circulating monocytes and neutrophils during reperfusion to levels below those present prior to ischemia. Furthermore, after 120 min of reperfusion, GdCl<sub>3 </sub>decreased ANAE and MPO activity in the myocardium by 1.9-fold and 6.5-fold respectively. GdCl<sub>3 </sub>decreased MPO activity to levels below those measured in the Sham group. Serum levels of the major neutrophil chemoattractant cytokine, IL-8 were increased from pre-ischemic levels during ischemia and reperfusion in both control and GdCl<sub>3 </sub>treated rats. Likewise, IL-8 levels increased throughout the 3 hour time period in the Sham group. There was no difference in IL-8 detected in the myocardium after 120 min reperfusion between groups. In contrast, after 120 min reperfusion GdCl<sub>3 </sub>decreased the myocardial tissue levels of macrophage secreted cytokines, GM-CSF and IL-1.</p> <p>Conclusion</p> <p>GdCl<sub>3 </sub>treatment prior to ischemia and reperfusion injury decreased circulating monocytes and neutrophils, macrophage secreted cytokines, and leukocyte infiltration into injured myocardium. These results suggest GdCl<sub>3 </sub>decreased monoctye and neutrophil migration and activation and may be a novel treatment for inflammation during ischemia and reperfusion.</p

    Complex Calculations during Cardiopulmonary Bypass—1987 Technology

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    (J. Extra-Corpor. Technol. 19[4]: p. 408-411 Winter 1987). Programmable calculators have become increasingly valuable to the conduct of cardiopulmonary bypass (CPB). We report the upgrading of our previous system with current technology. A Sharp PC-2500 portable microcomputer was chosen because of its low cost, easy programmability, rechargeable battery, and built-in printer. This system has allowed perfusionists to perform an increasing number of complex calculations with more accuracy and efficiency. In addition, it offers expanded memory and a permanent record of its calculations. We have used the new system in over 250 cases of CPB without problem. Although the flexibility of such a system allows customization to fit individual needs, we advise that any program be carefully tested and debugged to prevent serious mishap
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