Bafilomycin A1 Accelerates Chronic Refractory Wound Healing in db/db Mice.

Numerous studies have reported that autophagy plays an important role in chronic wound healing, and enhancement of autophagic activity impairs cutaneous wound healing. The autophagy inhibitor Bafilomycin A1 (Baf A1) inhibits autophagy by preventing the formation of autophagosomes. This study aimed a...

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Publicado en:BioMed Research International pp. 1 - 13
Autores principales: Wang, Fan, Zhang, Chao, Dai, Linna, Zhang, Yulu, Wang, Yongxue, Hao, Yongwei, Ji, Shenglu, Xu, Zhihao, Han, Na, Chen, Hongli, Zhang, Qiqing, Nan, Wenbin
Formato: pictorial research tables/charts Journal Article
Publicado: Wiley-Blackwell 7/3/2020
Acceso en línea:Ver este registro en EBSCOhost
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      dt: 7/3/2020
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      pub: Wiley-Blackwell
      place: Malden, Massachusetts
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        10.1155/2020/6265701
        144375006
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        atl: Bafilomycin A1 Accelerates Chronic Refractory Wound Healing in db/db Mice.
      aug:
        au:
          Wang, Fan
          Zhang, Chao
          Dai, Linna
          Zhang, Yulu
          Wang, Yongxue
          Hao, Yongwei
          Ji, Shenglu
          Xu, Zhihao
          Han, Na
          Chen, Hongli
          Zhang, Qiqing
          Nan, Wenbin
        affil: Life Science and Health Research Institute, College of Life Science and Technology, Xinxiang Medical University, Xinxiang, 453003 Henan, China
      sug:
        subj:
          Antibiotics, Macrolide Pharmacodynamics
          Blood Glucose Drug Effects
          Diabetes Mellitus Drug Therapy
          Wound Healing
          Animal Studies
          Mice
          Autophagy Drug Effects
          Epidermis Drug Effects
          Energy Metabolism Drug Effects
          Antigens Drug Effects
          Gene Expression Drug Effects
          Immunohistochemistry
          Collagen Drug Effects
          Staining and Labeling Methods
          Cytokines Drug Effects
          Tumor Necrosis Factor Drug Effects
          Cell Proliferation Drug Effects
      ab: Numerous studies have reported that autophagy plays an important role in chronic wound healing, and enhancement of autophagic activity impairs cutaneous wound healing. The autophagy inhibitor Bafilomycin A1 (Baf A1) inhibits autophagy by preventing the formation of autophagosomes. This study aimed at elucidating the effect of Bafilomycin A1 on chronic refractory wound healing in diabetic mice. A total of 40 diabetic (db/db) mice and 20 nondiabetic (db/m) mice were used in this study. Full-thickness skin defects were generated in the db/db mice models, which were then divided into the following two groups: the nontreated (db/db group) and Baf A1-treated groups (Baf A1 group). The same skin defects were generated in db/m mice (db/m group) to serve as a control. We demonstrated that Baf A1 treatment significantly accelerated wound healing in db/db mice and exerted good healing effects. Moreover, Baf A1 inhibited autophagy in the newly generated epidermis and had minor effects on metabolism in db/db mice. PCNA expression, as detected by immunohistochemistry, and collagen thickness, as detected by Masson's trichrome staining on the 14th day, were higher in the db/m and Baf A1 groups than in the db/db group. In addition, the expression of the proinflammatory cytokine TNF-α in the db/m and Baf A1 groups increased significantly on day 6, and the expression of the anti-inflammatory cytokine IL-10 also increased significantly on day 9. However, there were no significant changes in the expression levels of TNF-α and IL-10 in the db/db group. Therefore, Baf A1 may accelerate diabetic chronic refractory wound healing by promoting cell proliferation, collagen production, and regulating the inflammatory balance.
      pubtype: Academic Journal
      doctype:
        pictorial
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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