Anti-inflammatory, procollagen, and wound repair properties of topical insulin gel

胰岛素 伤口愈合 医学 糖尿病 胰岛素受体 天狼星红 IRS1 内科学 蛋白激酶B 内分泌学 H&E染色 免疫组织化学 胰岛素抵抗 信号转导 外科 化学 生物化学
作者
Priscila Peruzzo Apolinário,Flávia Cristina Zanchetta,Jéssica da Silva Cunha Breder,Gary G. Adams,Sílvio Roberto Consonni,Richard B. Gillis,Mário J.A. Saad,Maria Helena Melo Lima
出处
期刊:Brazilian Journal of Medical and Biological Research [Associação Brasileira de Divulgação Científica]
卷期号:56: e12640-e12640 被引量:12
标识
DOI:10.1590/1414-431x2023e12640
摘要

Diabetes mellitus is associated with impaired wound healing. The topical use of insulin is a promising therapy because it may favor all phases of the wound healing process. This study aimed to investigate the therapeutic outcomes of insulin gel in wounds of hyperglycemic mice. After diabetes induction, a 1-cm2 full-thickness wound was created on each animal's dorsum. The lesions were treated daily for 14 days with insulin gel (insulin group) or vehicle gel without insulin (vehicle group). Tissue samples were extracted on days 4, 7, 10, and 14 after the creation of the lesion. The samples were analyzed with hematoxylin/eosin and Sirius red staining, immunohistochemistry, Bio-Plex immunoassays, and western blotting. Insulin gel favored re-epithelialization at day 10 and increased the organization and deposition of collagen. Additionally, it modulated the expression of cytokines (interleukin (IL)-4 and IL-10) and increased the expression of arginase I, VEGF receptor 1, and VEGF on day 10. Activation of the insulin signaling pathway occurred via IRβ, IRS1, and IKK on day 10 and activation of Akt and IRS1 on day 14. These results suggested that insulin gel improved wound healing in hyperglycemic mice by modulating the expression of inflammatory factors, growth factors, and proteins of the insulin signaling pathway.
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