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S-thanatin enhances the efficacy of tigecycline in an experimental rat model of polymicrobial peritonitis.
S-thanatin enhances the efficacy of tigecycline in an experimental rat model of polymicrobial peritonitis.
- Source :
-
Peptides [Peptides] 2010 Jul; Vol. 31 (7), pp. 1231-6. Date of Electronic Publication: 2010 Apr 08. - Publication Year :
- 2010
-
Abstract
- We investigated the efficacy of the peptide s-thanatin alone and in combination with tigecycline in an animal model of sepsis induced by cecal ligation and puncture. Adult male Wistar rats were randomized to receive intravenously isotonic sodium chloride solution, 5mg/kg s-thanatin, 2mg/kg tigecycline, 5mg/kg s-thanatin combined with 2mg/kg tigecycline. The experiment was also performed with administration of the drugs 360 min after the surgical procedure to better investigate the clinical situation where there is an interval between the onset of sepsis and the initiation of therapy. Lethality, bacterial growth in blood, peritoneum, spleen and liver, and NO indices were evaluated. All compounds reduced the lethality when compared to control. In all experiments, the compounds reduced significantly bacterial growth and lethality compared with saline treatment. Treatment with s-thanatin resulted in significant decrease in plasma NO levels compared to tigecycline and control group. The combination between s-thanatin and tigecycline proved to be the most effective treatment in reducing all variables measured. S-thanatin may have potential therapeutic usefulness alone and when associated to tigecycline in polymicrobial peritonitis.<br /> (Copyright 2010 Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Disease Models, Animal
Male
Minocycline metabolism
Minocycline therapeutic use
Models, Animal
Peritonitis microbiology
Rats
Rats, Wistar
Tigecycline
Treatment Outcome
Anti-Bacterial Agents therapeutic use
Antimicrobial Cationic Peptides therapeutic use
Minocycline analogs & derivatives
Peritonitis drug therapy
Subjects
Details
- Language :
- English
- ISSN :
- 1873-5169
- Volume :
- 31
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Peptides
- Publication Type :
- Academic Journal
- Accession number :
- 20381561
- Full Text :
- https://doi.org/10.1016/j.peptides.2010.03.034