Your browser doesn't support javascript.
loading
Avenanthramide and ß-Glucan Therapeutics Accelerate Wound Healing Via Distinct and Nonoverlapping Mechanisms.
Kussie, Hudson C; Hahn, William; Sivaraj, Dharshan; Quintero, Filiberto; Knochel, Amelia; Alfsharif, Abdelrahman M; Yasmeh, Jonathan P; Fischer, Katharina; Mojadidi, Sultana; Hostler, Andrew; Granoski, Maia; McKenna, Eamonn; Henn, Dominic; Litmanovich, Ben; Miller, Abigail A; Schurr, Delaney K; Li, Vincent W; Li, William W; Gurtner, Geoffrey C; Chen, Kellen.
Afiliação
  • Kussie HC; Department of Surgery, University of Arizona, College of Medicine, Tucson, Arizona, USA.
  • Hahn W; Department of Surgery, University of Arizona, College of Medicine, Tucson, Arizona, USA.
  • Sivaraj D; Department of Surgery, University of Arizona, College of Medicine, Tucson, Arizona, USA.
  • Quintero F; Department of Surgery, University of Arizona, College of Medicine, Tucson, Arizona, USA.
  • Knochel A; Department of Surgery, University of Arizona, College of Medicine, Tucson, Arizona, USA.
  • Alfsharif AM; Department of Surgery, University of Arizona, College of Medicine, Tucson, Arizona, USA.
  • Yasmeh JP; Department of Surgery, University of Arizona, College of Medicine, Tucson, Arizona, USA.
  • Fischer K; Department of Surgery, University of Arizona, College of Medicine, Tucson, Arizona, USA.
  • Mojadidi S; Department of Surgery, University of Arizona, College of Medicine, Tucson, Arizona, USA.
  • Hostler A; Department of Surgery, University of Arizona, College of Medicine, Tucson, Arizona, USA.
  • Granoski M; Department of Surgery, University of Arizona, College of Medicine, Tucson, Arizona, USA.
  • McKenna E; Department of Surgery, University of Arizona, College of Medicine, Tucson, Arizona, USA.
  • Henn D; Department of Surgery, University of Arizona, College of Medicine, Tucson, Arizona, USA.
  • Litmanovich B; Department of Surgery, University of Arizona, College of Medicine, Tucson, Arizona, USA.
  • Miller AA; The Angiogenesis Foundation, Cambridge, Massachusetts, USA.
  • Schurr DK; The Angiogenesis Foundation, Cambridge, Massachusetts, USA.
  • Li VW; The Angiogenesis Foundation, Cambridge, Massachusetts, USA.
  • Li WW; The Angiogenesis Foundation, Cambridge, Massachusetts, USA.
  • Gurtner GC; Department of Surgery, University of Arizona, College of Medicine, Tucson, Arizona, USA.
  • Chen K; Department of Biomedical Engineering, University of Arizona, College of Medicine, Tucson, Arizona, USA.
Adv Wound Care (New Rochelle) ; 13(4): 155-166, 2024 04.
Article em En | MEDLINE | ID: mdl-38299969
ABSTRACT

Objective:

Given the significant economic, health care, and personal burden of acute and chronic wounds, we investigated the dose dependent wound healing mechanisms of two Avena sativa derived compounds avenanthramide (AVN) and ß-Glucan.

Approach:

We utilized a splinted excisional wound model that mimics human-like wound healing and performed subcutaneous AVN and ß-Glucan injections in 15-week-old C57BL/6 mice. Histologic and immunohistochemical analysis was performed on the explanted scar tissue to assess changes in collagen architecture and cellular responses.

Results:

AVN and ß-Glucan treatment provided therapeutic benefits at a 1% dose by weight in a phosphate-buffered saline vehicle, including accelerated healing time, beneficial cellular recruitment, and improved tissue architecture of healed scars. One percent AVN treatment promoted an extracellular matrix (ECM) architecture similar to unwounded skin, with shorter, more randomly aligned collagen fibers and reduced inflammatory cell presence in the healed tissue. One percent ß-Glucan treatment promoted a tissue architecture characterized by long, thick bundles of collagen with increased blood vessel density. Innovation AVN and ß-Glucan have previously shown promise in promoting wound healing, although the therapeutic efficacies and mechanisms of these bioactive compounds remain incompletely understood. Furthermore, the healed ECM architecture of these wounds has not been characterized.

Conclusions:

AVN and ß-Glucan accelerated wound closure compared to controls through distinct mechanisms. AVN-treated scars displayed a more regenerative tissue architecture with reduced inflammatory cell recruitment, while ß-Glucan demonstrated increased angiogenesis with more highly aligned tissue architecture more indicative of fibrosis. A deeper understanding of the mechanisms driving healing in these two naturally derived therapeutics will be important for translation to human use.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Animals Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Animals Idioma: En Ano de publicação: 2024 Tipo de documento: Article