dc.contributor.author | Shiehmorteza, M | |
dc.contributor.author | Ahmadi, A | |
dc.contributor.author | Abdollahi, M | |
dc.contributor.author | Nayebpour, M | |
dc.contributor.author | Mohammadi, M | |
dc.contributor.author | Hamishehkar, H | |
dc.contributor.author | Najaf, A | |
dc.contributor.author | Pazoki, M | |
dc.contributor.author | Mojtahedzadeh, M | |
dc.date.accessioned | 2018-08-26T09:33:25Z | |
dc.date.available | 2018-08-26T09:33:25Z | |
dc.date.issued | 2011 | |
dc.identifier.uri | http://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/57549 | |
dc.description.abstract | Background and the purpose of the study: Besides its hematopoietic effects, erythropoietin (EPO) by mobilization of iron and modulation of some inflammatory cytokines has antioxidant and anti-inflammatory properties. The purpose of this study was to evaluate these effects of erythropoietin and its impact on organ function in traumatized patients. Methods: Twenty-six ICU-admitted traumatized patients within 24 hrs after trauma were randomly assigned to the EPO (received EPO, 300 units/Kg/day) and Control (not received EPO) groups. The inflammatory biomarkers including Tumor Necrosis Factor alpha (TNF-?), Interleukin 1 (IL-1), Plasminogen Activator Inhibitor 1 (PAI-1) and Nitrotyrosine were recorded at the admission, 3, 6 and 9 days thereafter. Acute Physiology and Chronic Health Evaluation (APACHE II) and Sequential Organ Failure Assessment (SOFA) scores were also recorded. Results: Among 12 patients (EPO group) TNF-? level at the day of 9 (P=0.046), and within EPO group at the days of 3 (P=0.026 ameliorate), 6 (P=0.016), and 9 (P=0.052) were significantly lowered. Level of IL-1 and PAI-1 decreased significantly at days of 3, 6 and 9 post intervention. Also there were significant differences between two groups in the SOFA score during three measured time intervals (the first, third and seventh days).Conclusion: From the results of this study it seems that injection of erythrocyte stimulating agent is well tolerated and inhibits the inflammatory response and oxidative stress following trauma. | |
dc.language.iso | English | |
dc.relation.ispartof | DARU, Journal of Pharmaceutical Sciences | |
dc.subject | 3 nitrotyrosine | |
dc.subject | biological marker | |
dc.subject | interleukin 1 | |
dc.subject | plasminogen activator inhibitor | |
dc.subject | recombinant erythropoietin | |
dc.subject | tumor necrosis factor alpha | |
dc.subject | antiinflammatory activity | |
dc.subject | antioxidant activity | |
dc.subject | APACHE | |
dc.subject | article | |
dc.subject | clinical article | |
dc.subject | controlled study | |
dc.subject | drug effect | |
dc.subject | drug tolerability | |
dc.subject | human | |
dc.subject | inflammation | |
dc.subject | injury | |
dc.subject | intensive care unit | |
dc.subject | open study | |
dc.subject | oxidative stress | |
dc.subject | randomization | |
dc.subject | randomized controlled trial | |
dc.subject | scoring system | |
dc.title | Recombinant human erythropoietin reduces plasminogen activator inhibitor and ameliorates pro-infammatory responses following trauma | |
dc.type | Article | |
dc.citation.volume | 19 | |
dc.citation.issue | 2 | |
dc.citation.spage | 159 | |
dc.citation.epage | 165 | |
dc.citation.index | Scopus | |
dc.citation.URL | http://daru.tums.ac.ir/index.php/daru/article/view/431 | |