Testing the efficacy of antimicrobial peptides in the topical treatment of induced osteomyelitis in rats
Language English Country United States Media print-electronic
Document type Journal Article
Grant support
16-27726A
Ministerstvo Zdravotnictví Ceské Republiky
9777 and 6010
Internal grants of the Motol University Hospital
TA04010638
Technologická Agentura České Republiky
PubMed
28770427
DOI
10.1007/s12223-017-0540-9
PII: 10.1007/s12223-017-0540-9
Knihovny.cz E-resources
- MeSH
- Anti-Bacterial Agents administration & dosage MeSH
- Calcium Phosphates pharmacology MeSH
- Rats MeSH
- Humans MeSH
- Osteomyelitis drug therapy microbiology MeSH
- Peptides administration & dosage MeSH
- Rats, Wistar MeSH
- Staphylococcal Infections drug therapy microbiology MeSH
- Staphylococcus aureus drug effects physiology MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Humans MeSH
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Anti-Bacterial Agents MeSH
- calcium phosphate MeSH Browser
- Calcium Phosphates MeSH
- Peptides MeSH
Joint replacement infections and osteomyelitis are among the most serious complications in orthopaedics and traumatology. The risk factors for these infections are often bacterial resistance to antimicrobials. One of the few solutions available to control bacterial resistance involves antimicrobials, which have a different mechanism of action from traditional antibiotics. Antimicrobial peptides (AMP) appear to be highly promising candidates in the treatment of resistant infections. We have identified several AMP in the venom of various wild bees and designed analogues that show potent antimicrobial activity and low toxicity against eukaryotic cells. The aim of the present study was to test the efficacy of one of those synthetic peptide analogues for the treatment of acute osteomyelitis invoked in laboratory rats. Femoral cavities of 20 laboratory Wistar rats were infected with Staphylococcus aureus. After 1 week, eight rats received an injectable calcium phosphate carrier alone, another eight rats were treated with a calcium phosphate mixed with AMP, and four rats were left without any further treatment. After another week, all rats were euthanized and radiographs were made of both the operated and healthy limbs. The animals with the carrier alone exhibited more severe acute osteomyelitis on radiographs in comparison to the recipients of the calcium phosphate carrier loaded AMP and untreated infected individuals. Based on the results of the above mentioned experiment, it was concluded that when injected directly into the site of femoral acute osteomyelitis, the calcium phosphate carrier mixed with AMP reduced osteomyelitis signs visible on radiographs.
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Biomatter. 2012 Oct-Dec;2(4):176-94 PubMed
Amino Acids. 2010 Aug;39(3):763-75 PubMed
Nature. 2002 Jan 24;415(6870):389-95 PubMed
J Antimicrob Chemother. 2004 Dec;54(6):1078-84 PubMed
Biomaterials. 2010 Sep;31(25):6363-77 PubMed
Cell Mol Life Sci. 2011 Jul;68(13):2161-76 PubMed
J Nat Prod. 2016 Apr 22;79(4):1073-83 PubMed
Biopolymers. 2005;80(6):717-35 PubMed
J Chemother. 2013 Apr;25(2):67-80 PubMed
Clin Orthop Relat Res. 2005 Aug;(437):59-66 PubMed
Clin Microbiol Rev. 2000 Oct;13(4):686-707 PubMed
Eur J Clin Microbiol Infect Dis. 2000 Jun;19(6):403-17 PubMed
J Mol Microbiol Biotechnol. 2011;20(4):228-35 PubMed
Trends Biotechnol. 2011 Sep;29(9):464-72 PubMed
Eur Cell Mater. 2014 Mar 25;27:196-212 PubMed
J Orthop Res. 1996 Nov;14(6):914-20 PubMed
Swiss Med Wkly. 2005 Apr 30;135(17-18):243-51 PubMed
Clin Infect Dis. 1997 Dec;25(6):1303-9 PubMed
Adv Exp Med Biol. 2015;830:29-46 PubMed
Nat Biotechnol. 2006 Dec;24(12):1551-7 PubMed
Int J Antimicrob Agents. 2011 Sep;38(3):217-25 PubMed
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Pharmacol Rev. 2003 Mar;55(1):27-55 PubMed
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