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J Plast Reconstr Aesthet Surg ; 77: 416-429, 2023 02.
Article in English | MEDLINE | ID: mdl-36640596

ABSTRACT

This study aimed to investigate the wound-healing activity of animal platelet-rich plasma (PRP) in wounds infected with methicillin-resistant Staphylococcus aureus (MRSA) in rats. After wound induction, the rats were divided into three groups: noninfected animals treated with PRP (PRP group), MRSA-infected animals treated with mupirocin (standard control group), and MRSA-infected animals treated with PRP (MRSA+PRP group). Scratch assays, MTT test, and live/dead cells were also investigated. Total bacterial count, parameters of wound area, histopathological assessment, and expressions of IL-1ß, TNF-α, iNOS, PDGF, FGF-2, and TGF-ß mRNA levels and immunofluorescent staining of CD31 and collagen type 1 were assessed. The results showed that culture with PRP increased migration. PRP only showed cytotoxicity in a concentration of 100%. Topical application of PRP (50 µL) reduced the wound area and total bacterial count compared with the control group (P<0.05). The mRNA levels of IL-1ß, TNF-α, and iNOS expression on days 7 and 14 (P<0.05) decreased in the treated groups compared with control rats. The mRNA levels of PDGF and TGF-ß expression (P<0.05) increased in the treatment groups compared with control rats on days 3 and 7 (P<0.05). FGF-2 expression was significantly higher in the treated groups compared with the control group on days 7 and 14 (P<0.05). Moreover, positive expressions of macrophage colony-stimulating factor (M-CSF), CD31, collagen type 1 and cytokeratin proteins keratinocyte proliferation, and re-epithelization were significantly (P<0.05) increased in both PRP and MRSA+PRP-treated groups compared with the control groups on days 7 and 14. Topical administration of PRP accelerated the wound healing in MRSA-infected wound by decreasing the inflammation and improving the proliferative phase.


Subject(s)
Methicillin-Resistant Staphylococcus aureus , Platelet-Rich Plasma , Wound Infection , Rats , Animals , Methicillin-Resistant Staphylococcus aureus/metabolism , Tumor Necrosis Factor-alpha/metabolism , Fibroblast Growth Factor 2 , Wound Healing , Platelet-Rich Plasma/metabolism , Collagen Type I/metabolism , Transforming Growth Factor beta/metabolism , Administration, Topical , RNA, Messenger/metabolism
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