Use of wound edge inversion (epibole) to generate recalcitrant and inflamed diabetic wounds. Issue 1 (2nd September 2022)
- Record Type:
- Journal Article
- Title:
- Use of wound edge inversion (epibole) to generate recalcitrant and inflamed diabetic wounds. Issue 1 (2nd September 2022)
- Main Title:
- Use of wound edge inversion (epibole) to generate recalcitrant and inflamed diabetic wounds
- Authors:
- Lee, Phoebe L.
Loder, Shawn J.
Guerrero, David T.
Nerone, W. Vincent
Bengur, Fuat Baris
Rubin, J. Peter
Kokai, Lauren E. - Abstract:
- Abstract: Robust and predictive pre‐clinical models of recalcitrant diabetic wounds are critical for advancing research efforts toward improving healing. Murine models have logistic and genetic benefits versus larger animals; however, native murine healing inadequately represents clinically recalcitrant wounds in humans. Furthermore, current humanization techniques employing devices, deleterious mutations or chemical agents each carry model‐specific limitations. To better replicate human wounds in a mouse, we developed a novel wound‐edge inversion (WEI) technique that mimics the architecture of epibole and mitigates contracture, epithelialization, and consequently wound closure. In this study, we evaluated the reliability and durability of the WEI model in wild‐type and obese diabetic mice and compared to healing after (i) punch biopsy, (ii) mechanical/silicone stenting or (iii) exogenous oxidative stressors. In wild‐type mice, WEI demonstrated favourable closure characteristics compared to both control and stented wounds, however, wounds progressed to closure by 4 weeks. In contrast, diabetic WEI wounds persisted for 6–10 weeks with reduced contracture and epithelialization. In both diabetic and wild‐type mice, WEI sites demonstrated persistence of inflammatory populations, absence of epithelialization, and histologic presence of alpha‐SMA positive granulation tissue when compared to controls. We conclude that the WEI technique is particularly valuable for modellingAbstract: Robust and predictive pre‐clinical models of recalcitrant diabetic wounds are critical for advancing research efforts toward improving healing. Murine models have logistic and genetic benefits versus larger animals; however, native murine healing inadequately represents clinically recalcitrant wounds in humans. Furthermore, current humanization techniques employing devices, deleterious mutations or chemical agents each carry model‐specific limitations. To better replicate human wounds in a mouse, we developed a novel wound‐edge inversion (WEI) technique that mimics the architecture of epibole and mitigates contracture, epithelialization, and consequently wound closure. In this study, we evaluated the reliability and durability of the WEI model in wild‐type and obese diabetic mice and compared to healing after (i) punch biopsy, (ii) mechanical/silicone stenting or (iii) exogenous oxidative stressors. In wild‐type mice, WEI demonstrated favourable closure characteristics compared to both control and stented wounds, however, wounds progressed to closure by 4 weeks. In contrast, diabetic WEI wounds persisted for 6–10 weeks with reduced contracture and epithelialization. In both diabetic and wild‐type mice, WEI sites demonstrated persistence of inflammatory populations, absence of epithelialization, and histologic presence of alpha‐SMA positive granulation tissue when compared to controls. We conclude that the WEI technique is particularly valuable for modelling recalcitrant diabetic wounds with sustained inflammation and dysfunctional healing. … (more)
- Is Part Of:
- Wound repair and regeneration. Volume 31:Issue 1(2023)
- Journal:
- Wound repair and regeneration
- Issue:
- Volume 31:Issue 1(2023)
- Issue Display:
- Volume 31, Issue 1 (2023)
- Year:
- 2023
- Volume:
- 31
- Issue:
- 1
- Issue Sort Value:
- 2023-0031-0001-0000
- Page Start:
- 120
- Page End:
- 127
- Publication Date:
- 2022-09-02
- Subjects:
- chronic wounds -- diabetes -- surgical models -- wound healing
Wound healing -- Periodicals
Regeneration (Biology) -- Periodicals
617.14 - Journal URLs:
- http://firstsearch.oclc.org ↗
http://firstsearch.oclc.org/journal=1067-1927;screen=info;ECOIP ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1524-475X ↗
http://www.blackwell-synergy.com/member/institutions/issuelist.asp?journal=wrr ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/wrr.13046 ↗
- Languages:
- English
- ISSNs:
- 1067-1927
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 9364.529320
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 25145.xml