Effect of FC43se on Endotoxin-induced Disseminated Intravascular Coagulation in Rats
Hiroshima Journal of Medical Sciences Volume 48 Issue 2
Page 71-77
published_at 1999-06
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Title ( eng ) |
Effect of FC43se on Endotoxin-induced Disseminated Intravascular Coagulation in Rats
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Creator |
Ochikubo Hiroyuki
Wada Seishi
Sugawara Yuji
Matsuura Yuichiro
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Source Title |
Hiroshima Journal of Medical Sciences
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Volume | 48 |
Issue | 2 |
Start Page | 71 |
End Page | 77 |
Journal Identifire |
[PISSN] 0018-2052
[EISSN] 2433-7668
[NCID] AA00664312
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Abstract |
Perfluorotributylamine/Pluronic F68 Stem-Emulsion (FC43se), which is a blood substitute, was assessed for its effectiveness on disseminated intravascular coagulation (DIC) in the rat model. Rats were infused intravenously with 2.5 mg/kg of Escherichia coli lipopolysaccharide (Escherichia coli 055:B5 lipopolysaccharide B) for four hours. At the same time, FC43se or normal physiological saline was infused at 2.5 ml/kg/hr. The white blood cell and platelet counts, prothrombin time (PT), activated partial thromboplastin time (APTT), and the plasma levels of interleukin-1 beta (IL-1β), interleukin-4 (IL-4), interleukin-6 (IL-6), interleukin-10 (IL-10), and tumor necrosis factor alpha (TNFα) were determined at 4hr. The infusion of FC43se markedly prevented a decrease in platelet counts (p=0.0004) and a prolongation of both PT and APTT (p<0.05 and p<0.03 each). The serum level of IL-1βand IL-4 showed no significant change. The serum level of IL-6, IL-10 and TNFα increased significantly (p=0.0007, p=0.0004 and p<0.05 each) with infusion of FC43se in rats treated with bacterial endotoxin. FC43se has beneficial effects on endotoxin-induced DIC as an anticoagulant and anti-inflammatory cytokine induced agent.
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Keywords |
Perfiuorocarbons
Disseminated intravascular coagulation
Cytokine
Endotoxin
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NDC |
Medical sciences [ 490 ]
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Language |
eng
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Resource Type | departmental bulletin paper |
Publisher |
Hiroshima University Medical Press
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Date of Issued | 1999-06 |
Publish Type | Version of Record |
Access Rights | open access |
Source Identifier |
[ISSN] 0018-2052
[NCID] AA00664312
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