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Effect of Hominis Placenta on cutaneous wound healing in normal and diabetic mice

BACKGROUND/OBJECTIVES: The number of diabetic patients has recently shown a rapid increase, and delayed wound healing is a major clinical complication in diabetes. In this study, the wound healing effect of Hominis placenta (HP) treatment was investigated in normal and streptozotocin-induced diabeti...

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Autores principales: Park, Ji-Yeun, Lee, Jiyoung, Jeong, Minsu, Min, Seorim, Kim, Song-Yi, Lee, Hyejung, Lim, Yunsook, Park, Hi-Joon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Nutrition Society and the Korean Society of Community Nutrition 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4122712/
https://www.ncbi.nlm.nih.gov/pubmed/25110560
http://dx.doi.org/10.4162/nrp.2014.8.4.404
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author Park, Ji-Yeun
Lee, Jiyoung
Jeong, Minsu
Min, Seorim
Kim, Song-Yi
Lee, Hyejung
Lim, Yunsook
Park, Hi-Joon
author_facet Park, Ji-Yeun
Lee, Jiyoung
Jeong, Minsu
Min, Seorim
Kim, Song-Yi
Lee, Hyejung
Lim, Yunsook
Park, Hi-Joon
author_sort Park, Ji-Yeun
collection PubMed
description BACKGROUND/OBJECTIVES: The number of diabetic patients has recently shown a rapid increase, and delayed wound healing is a major clinical complication in diabetes. In this study, the wound healing effect of Hominis placenta (HP) treatment was investigated in normal and streptozotocin-induced diabetic mice. MATERIALS/METHODS: Four full thickness wounds were created using a 4 mm biopsy punch on the dorsum. HP was injected subcutaneously at the middle region of the upper and lower wounds. Wounds were digitally photographed and wound size was measured every other day until the 14th day. Wound closure rate was analyzed using CANVAS 7SE software. Wound tissues were collected on days 2, 6, and 14 after wounding for H/E, immunohistochemistry for FGF2, and Masson's trichrome staining for collagen study. RESULTS: Significantly faster wound closure rates were observed in the HP treated group than in normal and diabetes control mice on days 6 and 8. Treatment with HP resulted in reduced localization of inflammatory cells in wounded skin at day 6 in normal mice and at day 14 in diabetic mice (P < 0.01). Expression of fibroblast growth factor (FGF) 2 showed a significant increase in the HP treated group on day 14 in both normal (P < 0.01) and diabetic mice (P < 0.05). In addition, HP treated groups showed a thicker collagen layer than no treatment groups, which was remarkable on the last day, day 14, in both normal and diabetic mice. CONCLUSIONS: Taken together, HP treatment has a beneficial effect on acceleration of cutaneous wound healing via regulation of the entire wound healing process, including inflammation, proliferation, and remodeling.
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spelling pubmed-41227122014-08-10 Effect of Hominis Placenta on cutaneous wound healing in normal and diabetic mice Park, Ji-Yeun Lee, Jiyoung Jeong, Minsu Min, Seorim Kim, Song-Yi Lee, Hyejung Lim, Yunsook Park, Hi-Joon Nutr Res Pract Original Research BACKGROUND/OBJECTIVES: The number of diabetic patients has recently shown a rapid increase, and delayed wound healing is a major clinical complication in diabetes. In this study, the wound healing effect of Hominis placenta (HP) treatment was investigated in normal and streptozotocin-induced diabetic mice. MATERIALS/METHODS: Four full thickness wounds were created using a 4 mm biopsy punch on the dorsum. HP was injected subcutaneously at the middle region of the upper and lower wounds. Wounds were digitally photographed and wound size was measured every other day until the 14th day. Wound closure rate was analyzed using CANVAS 7SE software. Wound tissues were collected on days 2, 6, and 14 after wounding for H/E, immunohistochemistry for FGF2, and Masson's trichrome staining for collagen study. RESULTS: Significantly faster wound closure rates were observed in the HP treated group than in normal and diabetes control mice on days 6 and 8. Treatment with HP resulted in reduced localization of inflammatory cells in wounded skin at day 6 in normal mice and at day 14 in diabetic mice (P < 0.01). Expression of fibroblast growth factor (FGF) 2 showed a significant increase in the HP treated group on day 14 in both normal (P < 0.01) and diabetic mice (P < 0.05). In addition, HP treated groups showed a thicker collagen layer than no treatment groups, which was remarkable on the last day, day 14, in both normal and diabetic mice. CONCLUSIONS: Taken together, HP treatment has a beneficial effect on acceleration of cutaneous wound healing via regulation of the entire wound healing process, including inflammation, proliferation, and remodeling. The Korean Nutrition Society and the Korean Society of Community Nutrition 2014-08 2014-05-15 /pmc/articles/PMC4122712/ /pubmed/25110560 http://dx.doi.org/10.4162/nrp.2014.8.4.404 Text en ©2014 The Korean Nutrition Society and the Korean Society of Community Nutrition http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Park, Ji-Yeun
Lee, Jiyoung
Jeong, Minsu
Min, Seorim
Kim, Song-Yi
Lee, Hyejung
Lim, Yunsook
Park, Hi-Joon
Effect of Hominis Placenta on cutaneous wound healing in normal and diabetic mice
title Effect of Hominis Placenta on cutaneous wound healing in normal and diabetic mice
title_full Effect of Hominis Placenta on cutaneous wound healing in normal and diabetic mice
title_fullStr Effect of Hominis Placenta on cutaneous wound healing in normal and diabetic mice
title_full_unstemmed Effect of Hominis Placenta on cutaneous wound healing in normal and diabetic mice
title_short Effect of Hominis Placenta on cutaneous wound healing in normal and diabetic mice
title_sort effect of hominis placenta on cutaneous wound healing in normal and diabetic mice
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4122712/
https://www.ncbi.nlm.nih.gov/pubmed/25110560
http://dx.doi.org/10.4162/nrp.2014.8.4.404
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