Effect of intermittent fasting on saving zone of stasis in burn wounds in rats

Burns. 2023 Jun;49(4):901-913. doi: 10.1016/j.burns.2022.06.010. Epub 2022 Jun 22.

Abstract

Background: Intermittent Fasting (IF) has proved to have various positive effects on life span, diseases, and healing of tissues in rodents. We evaluated the protective effect of fasting in maintaining the ischemic zones in burn wounds.

Methods: In this study, 20 rats were divided into two groups where the IF rats were deprived of food for three months. Burn wounds were created by burn comb model on the back of all rats. On days 3 and 21 after injury, five rats in each group were euthanized whereby samples were collected for histopathological, immunohistochemical (Bcl2, P53 and VEGF), and biochemical (MDA, TAC, HP) evaluations.

Results: Histopathological analysis revealed epithelial layer and zone of ischemia remained viable in the intermittent fasting group on day 3. On the 21st day, epithelialization, angiogenesis, inflammation, fibrocyte-fibroblast, and collagen density were different in the ischemic and necrotic zones between the control and intermittent fasting groups (p<0.05). We found no statistical differences in Bcl2, P53, VEGF, MDA, TAC, and HP on day 3 between the intermittent fasting and control groups.

Conclusions: Intermittent fasting before burn wounds reduces tissue damage caused by ischemia and enhanced the viability of cells in zone of stasis. It also accelerated wound healing by increasing epithelialization and collagen production in the skin and regulating inflammatory responses. This intervention appears to be related to better collagen arrangement and angiogenesis.

Keywords: Burn wound healing; Intermittent fasting; Ischemia.

MeSH terms

  • Animals
  • Burns* / pathology
  • Intermittent Fasting*
  • Ischemia / pathology
  • Rats
  • Skin / pathology
  • Tumor Suppressor Protein p53 / pharmacology
  • Vascular Endothelial Growth Factor A

Substances

  • Vascular Endothelial Growth Factor A
  • Tumor Suppressor Protein p53