Topical application of the lectin A rtin M accelerates wound healing in rat oral mucosa by enhancing TGF ‐β and VEGF production

The lectin A rtin M has been shown to accelerate the wound‐healing process. The aims of this study were to evaluate the effects of A rtin M on wound healing in the palatal mucosa of rats and to investigate the effects of A rtin M on transforming growth factor beta ( TGF ‐β) and vascular endothelial...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Wound repair and regeneration 2013-05, Vol.21 (3), p.456-463
Hauptverfasser: Kim, Yeon J., Carvalho, Fernanda C., Souza, João A.C., Gonçalves, Pedro C.G., Nogueira, Andressa V.B., Spolidório, Luis C., Roque‐Barreira, Maria C., Cirelli, Joni A.
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:The lectin A rtin M has been shown to accelerate the wound‐healing process. The aims of this study were to evaluate the effects of A rtin M on wound healing in the palatal mucosa of rats and to investigate the effects of A rtin M on transforming growth factor beta ( TGF ‐β) and vascular endothelial growth factor ( VEGF ) secretion by rat gingival fibroblasts. A surgical wound was created on the palatal mucosa of 72 rats divided into three groups according to treatment: C — C ontrol (nontreated), A — A rtin M gel, and V — V ehicle. Eight animals per group were sacrificed at 3, 5, and 7 days postsurgery for histology, immunohistochemistry and determination of the levels of cytokines, and growth factors. Gingival fibroblasts were incubated with 2.5 μg/m L of A rtin M for 24, 48, and 72 hours. The expression of VEGF and TGF ‐β was determined by enzyme‐linked immunosorbent assay. Histologically, at day 7, the A rtin M group showed earlier reepithelialization, milder inflammatory infiltration, and increased collagen fiber formation, resulting in faster maturation of granular tissue than in the other groups ( p  
ISSN:1067-1927
1524-475X
DOI:10.1111/wrr.12041