Topical Insulin Accelerates Wound Healing in Diabetes by Enhancing the AKT and ERK Pathways: A Double-Blind Placebo-Controlled Clinical Trial


Autoria(s): Lima, Maria H. M.; Caricilli, Andrea Moro; de Abreu, Lelia L.; Araujo, Eliana Pereira de; Pelegrinelli, Fabiana F.; Thirone, Ana C. P.; Tsukumo, Daniela M.; Pessoa, Ana Flavia M.; Santos, Marinilce Fagundes dos; de Moraes, Maria A.; Carvalheira, José Barreto Campello; Velloso, Lício Augusto; Saad, Mario Jose Abdalla
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

04/11/2013

04/11/2013

2012

Resumo

Background: Wound healing is impaired in diabetes mellitus, but the mechanisms involved in this process are virtually unknown. Proteins belonging to the insulin signaling pathway respond to insulin in the skin of rats. Objective: The purpose of this study was to investigate the regulation of the insulin signaling pathway in wound healing and skin repair of normal and diabetic rats, and, in parallel, the effect of a topical insulin cream on wound healing and on the activation of this pathway. Research Design and Methods: We investigated insulin signaling by immunoblotting during wound healing of control and diabetic animals with or without topical insulin. Diabetic patients with ulcers were randomized to receive topical insulin or placebo in a prospective, double-blind and placebo-controlled, randomized clinical trial (NCT 01295177) of wound healing. Results and Conclusions: Expression of IR, IRS-1, IRS-2, SHC, ERK, and AKT are increased in the tissue of healing wounds compared to intact skin, suggesting that the insulin signaling pathway may have an important role in this process. These pathways were attenuated in the wounded skin of diabetic rats, in parallel with an increase in the time of complete wound healing. Upon topical application of insulin cream, the wound healing time of diabetic animals was normalized, followed by a reversal of defective insulin signal transduction. In addition, the treatment also increased expression of other proteins, such as eNOS (also in bone marrow), VEGF, and SDF-1 alpha in wounded skin. In diabetic patients, topical insulin cream markedly improved wound healing, representing an attractive and cost-free method for treating this devastating complication of diabetes.

Sao Paulo Research Foundation (FAPESP)

Sao Paulo Research Foundation (FAPESP)

National Institute of Science and Technology (INCT)

National Institute of Science and Technology (INCT)

National Council for Scientific and Technological Development (CNPq)

National Council for Scientific and Technological Development (CNPq)

Identificador

PLOS ONE, SAN FRANCISCO, v. 7, n. 5, supl. 1, Part 2, pp. 174-181, MAY 25, 2012

1932-6203

http://www.producao.usp.br/handle/BDPI/37807

10.1371/journal.pone.0036974

http://dx.doi.org/10.1371/journal.pone.0036974

Idioma(s)

eng

Publicador

PUBLIC LIBRARY SCIENCE

SAN FRANCISCO

Relação

PLOS ONE

Direitos

openAccess

Copyright PUBLIC LIBRARY SCIENCE

Palavras-Chave #RECEPTOR TYROSINE KINASE #HUMAN-SKIN FIBROBLASTS #NITRIC-OXIDE SYNTHASE #GROWTH FACTOR-BB #PROTEIN-KINASE #EPIDERMAL-KERATINOCYTES #ENDOTHELIAL-CELLS #ULCERS #ACTIVATION #GLUCOSE #MULTIDISCIPLINARY SCIENCES
Tipo

article

original article

publishedVersion