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J Surg Res ; 100(2): 183-8, 2001 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-11592790

RESUMO

BACKGROUND: A rat model was used to investigate the efficacy of a polycationic peptide, the polymyxin-like ranalexin, in the prevention of lethality in a rat model of septic shock. The effect of ranalexin was compared with those of polymyxin B and imipenem. METHODS: Adult male Wistar rats (weight range: 250-300 g) were used for all the experiments. The study included five groups: an uninfected control group C(0), an untreated control group C(1), and three drug-treated groups that received 1 mg/kg ranalexin (group 2), 20 mg/kg imipenem (group 3), and 3 mg/kg polymyxin B (group 4). Rats, with the exception of the uninfected control group (C(0)), were given an intraperitoneal injection of 2 x 10(10) colony-forming units of Escherichia coli. Each group included 15 animals. Bacterial growth in abdominal exudate and plasma; endotoxin and tumor necrosis factor alpha (TNF-alpha) concentrations in plasma, and mortality were evaluated. RESULTS: Results were evaluated 48 h after inoculation. Ranalexin, imipenem, and polymyxin B significantly reduced the lethality (survival was 93.3, 80.0, and 93.3%, respectively) and the growth of E. coli both in abdominal fluid and plasma compared with saline treatment. Ranalexin showed higher antimicrobial activity than polymyxin B and imipenem and, at the same time, exhibited an antiendotoxin activity similar to that of polymyxin B (< or =0.015 EU/mL). Finally, ranalexin and polymyxin B significantly reduced plasma TNF-alpha levels (< or =4 pg/mL). CONCLUSION: Monodose ranalexin treatment prevents bacterial growth, endotoxemia, and mortality in rats with septic shock.


Assuntos
Anti-Infecciosos/farmacologia , Endotoxemia/tratamento farmacológico , Peptídeos Cíclicos/farmacologia , Animais , Antibacterianos/farmacologia , Modelos Animais de Doenças , Endotoxemia/mortalidade , Infecções por Escherichia coli/tratamento farmacológico , Infecções por Escherichia coli/mortalidade , Imipenem/farmacologia , Masculino , Polimixina B/farmacologia , Polimixinas , Ratos , Taxa de Sobrevida , Tienamicinas/farmacologia , Fator de Necrose Tumoral alfa/metabolismo
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