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Betulinic Acid Enhances the Viability of Random-Pattern Skin Flaps by Activating Autophagy

Random-pattern skin flap replantation is commonly used to repair skin defects during plastic and reconstructive surgery. However, flap necrosis due to ischemia and ischemia–reperfusion injury limits clinical applications. Betulinic acid, a plant-derived pentacyclic triterpene, may facilitate flap su...

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Autores principales: Li, Jiafeng, Bao, Guodong, ALyafeai, Eman, Ding, Jian, Li, Shihen, Sheng, Shimin, Shen, Zitong, Jia, Zhenyu, Lin, Chen, Zhang, Chenxi, Lou, Zhiling, Xu, Huazi, Gao, Weiyang, Zhou, Kailiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6753397/
https://www.ncbi.nlm.nih.gov/pubmed/31572190
http://dx.doi.org/10.3389/fphar.2019.01017
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author Li, Jiafeng
Bao, Guodong
ALyafeai, Eman
Ding, Jian
Li, Shihen
Sheng, Shimin
Shen, Zitong
Jia, Zhenyu
Lin, Chen
Zhang, Chenxi
Lou, Zhiling
Xu, Huazi
Gao, Weiyang
Zhou, Kailiang
author_facet Li, Jiafeng
Bao, Guodong
ALyafeai, Eman
Ding, Jian
Li, Shihen
Sheng, Shimin
Shen, Zitong
Jia, Zhenyu
Lin, Chen
Zhang, Chenxi
Lou, Zhiling
Xu, Huazi
Gao, Weiyang
Zhou, Kailiang
author_sort Li, Jiafeng
collection PubMed
description Random-pattern skin flap replantation is commonly used to repair skin defects during plastic and reconstructive surgery. However, flap necrosis due to ischemia and ischemia–reperfusion injury limits clinical applications. Betulinic acid, a plant-derived pentacyclic triterpene, may facilitate flap survival. In the present study, the effects of betulinic acid on flap survival and the underlying mechanisms were assessed. Fifty-four mice with a dorsal random flap model were randomly divided into the control, betulinic acid group, and the betulinic acid + 3-methyladenine group. These groups were treated with dimethyl sulfoxide, betulinic acid, and betulinic acid plus 3-methyladenine, respectively. Flap tissues were acquired on postoperative day 7 to assess angiogenesis, apoptosis, oxidative stress, and autophagy. Betulinic acid promoted survival of the skin flap area, reduced tissue edema, and enhanced the number of microvessels. It also enhanced angiogenesis, attenuated apoptosis, alleviated oxidative stress, and activated autophagy. However, its effects on flap viability and angiogenesis, apoptosis, and oxidative stress were reversed by the autophagy inhibitor 3-methyladenine. Our findings reveal that betulinic acid improves survival of random-pattern skin flaps by promoting angiogenesis, dampening apoptosis, and alleviating oxidative stress, which mediates activation of autophagy.
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spelling pubmed-67533972019-09-30 Betulinic Acid Enhances the Viability of Random-Pattern Skin Flaps by Activating Autophagy Li, Jiafeng Bao, Guodong ALyafeai, Eman Ding, Jian Li, Shihen Sheng, Shimin Shen, Zitong Jia, Zhenyu Lin, Chen Zhang, Chenxi Lou, Zhiling Xu, Huazi Gao, Weiyang Zhou, Kailiang Front Pharmacol Pharmacology Random-pattern skin flap replantation is commonly used to repair skin defects during plastic and reconstructive surgery. However, flap necrosis due to ischemia and ischemia–reperfusion injury limits clinical applications. Betulinic acid, a plant-derived pentacyclic triterpene, may facilitate flap survival. In the present study, the effects of betulinic acid on flap survival and the underlying mechanisms were assessed. Fifty-four mice with a dorsal random flap model were randomly divided into the control, betulinic acid group, and the betulinic acid + 3-methyladenine group. These groups were treated with dimethyl sulfoxide, betulinic acid, and betulinic acid plus 3-methyladenine, respectively. Flap tissues were acquired on postoperative day 7 to assess angiogenesis, apoptosis, oxidative stress, and autophagy. Betulinic acid promoted survival of the skin flap area, reduced tissue edema, and enhanced the number of microvessels. It also enhanced angiogenesis, attenuated apoptosis, alleviated oxidative stress, and activated autophagy. However, its effects on flap viability and angiogenesis, apoptosis, and oxidative stress were reversed by the autophagy inhibitor 3-methyladenine. Our findings reveal that betulinic acid improves survival of random-pattern skin flaps by promoting angiogenesis, dampening apoptosis, and alleviating oxidative stress, which mediates activation of autophagy. Frontiers Media S.A. 2019-09-13 /pmc/articles/PMC6753397/ /pubmed/31572190 http://dx.doi.org/10.3389/fphar.2019.01017 Text en Copyright © 2019 Li, Bao, ALyafeai, Ding, Li, Sheng, Shen, Jia, Lin, Zhang, Lou, Xu, Gao and Zhou http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Li, Jiafeng
Bao, Guodong
ALyafeai, Eman
Ding, Jian
Li, Shihen
Sheng, Shimin
Shen, Zitong
Jia, Zhenyu
Lin, Chen
Zhang, Chenxi
Lou, Zhiling
Xu, Huazi
Gao, Weiyang
Zhou, Kailiang
Betulinic Acid Enhances the Viability of Random-Pattern Skin Flaps by Activating Autophagy
title Betulinic Acid Enhances the Viability of Random-Pattern Skin Flaps by Activating Autophagy
title_full Betulinic Acid Enhances the Viability of Random-Pattern Skin Flaps by Activating Autophagy
title_fullStr Betulinic Acid Enhances the Viability of Random-Pattern Skin Flaps by Activating Autophagy
title_full_unstemmed Betulinic Acid Enhances the Viability of Random-Pattern Skin Flaps by Activating Autophagy
title_short Betulinic Acid Enhances the Viability of Random-Pattern Skin Flaps by Activating Autophagy
title_sort betulinic acid enhances the viability of random-pattern skin flaps by activating autophagy
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6753397/
https://www.ncbi.nlm.nih.gov/pubmed/31572190
http://dx.doi.org/10.3389/fphar.2019.01017
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