Improved cutaneous wound healing after intraperitoneal injection of alpha-melanocyte-stimulating hormone

被引:32
作者
de Souza, Kenia Soares [1 ]
Cantaruti, Thiago Anselmo [1 ]
Azevedo Junior, Geraldo Magela [1 ,2 ]
de Almeida Galdino, Daniel Antero [1 ]
Rodrigues, Claudiney Melquiades [1 ]
Costa, Raquel Alves [1 ,3 ]
Vaz, Nelson Monteiro [4 ]
Carvalho, Claudia Rocha [1 ]
机构
[1] Univ Fed Minas Gerais, Dept Morfol, BR-31270901 Belo Horizonte, MG, Brazil
[2] Hosp Publ Reg Betim, Belo Horizonte, MG, Brazil
[3] Univ Fed Sao Joao del Rey, Belo Horizonte, MG, Brazil
[4] Univ Fed Minas Gerais, Dept Bioquim & Imunol, BR-31270901 Belo Horizonte, MG, Brazil
关键词
alpha-melanocyte-stimulating hormone and scarless healing inflammation; scars; wound healing; MELANOCORTIN PEPTIDES; SCAR FORMATION; ANTIINFLAMMATORY ACTIONS; FUTURE PERSPECTIVES; IMMUNE-SYSTEM; IN-VITRO; SKIN; MSH; FETAL; INFLAMMATION;
D O I
10.1111/exd.12609
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Skin wound healing is a complex process involving many types of cells and molecules and often results in scar tissue formation in adult mammals. However, scarless healing occurs in foetal skin and minimal scars may occur after cutaneous healing in the adult with reduced inflammation. Alpha-melanocyte-stimulating hormone (alpha-MSH) is widely distributed within the central nervous system and in other body regions, such as the skin, and has strong anti-inflammatory activity. The aim in the present experiments was to learn whether intraperitoneal (i.p) injection of alpha-MSH just before skin wounds antagonize inflammation and improves skin wound healing in adult mice. C57BL/6 young adult mice received an i.p. injection of 1 mg/kg of alpha-MSH and, 30 min later, two circular through-and-through holes (6.5 mm diameter) were made in their dorsal skin under anaesthesia. Control mice were wounded after vehicle injection. The wound healing process was analysed macroscopically and microscopically at 3, 7, 40 and 60 days. Skin samples were fixed in formalin, embedded in paraffin, sectioned at 5 mu m, stained with H&E or toluidine blue for cell analysis or Gomori's trichrome for extracellular matrix (ECM) analysis. Other samples were fixed in DMSO+methanol, embedded in paraplast and incubated with anti-CD45, antismooth muscle actin, anticollagen-I and anticollagen-III for immunofluorescence analysis. Alpha-MSH significantly reduced the number of leucocytes, mast cells and fibroblasts at 3 and 7 days after injury. On days 40 and 60, alpha-MSH reduced scar area and improved the organization of the collagen fibres indicating that it may direct the healing into a more-regenerative/less-scarring pathway.
引用
收藏
页码:198 / 203
页数:6
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