Tetrahydropalmatine promotes random skin flap survival in rats via the PI3K/AKT signaling pathway

J Ethnopharmacol. 2024 Apr 24:324:117808. doi: 10.1016/j.jep.2024.117808. Epub 2024 Jan 26.

Abstract

Ethnopharmacological relevance: Flap necrosis is the most common complication after flap transplantation, but its prevention remains challenging. Tetrahydropalmatine (THP) is the main bioactive component of the traditional Chinese medicine Corydalis yanhusuo, with effects that include the activation of blood circulation, the promotion of qi, and pain relief. Although THP is widely used to treat various pain conditions, its impact on flap survival is unknown.

Aim of the study: To explore the effect and mechanism of THP on skin flap survival.

Materials and methods: In this study, we established a modified McFarlane flap model, and the flap survival rate was calculated after 7 days of THP treatment. Angiogenesis and blood perfusion were evaluated using lead oxide/gelatin angiography and laser Doppler, respectively. Flap tissue obtained from zone II was evaluated histopathologically, by hematoxylin and eosin staining, and in assays for malondialdehyde content and superoxide dismutase activity. Immunofluorescence was performed to detect interleukin (IL)-6, tumor necrosis factor (TNF)-α, hypoxia-inducible factor (HIF)-1α, Bcl-2, Bax, caspase-3, caspase-9, SQSTM1/P62, Beclin-1, and LC3 expression, and Western blot to assess PI3K/AKT signaling pathway activation and Vascular endothelial growth factor (VEGF) expression. The role played by the autophagy pathway in flap necrosis was examined using rapamycin, a specific inhibitor of mTOR.

Results: Experimentally, THP improved the survival rate of skin flaps, promoted angiogenesis, and improved blood perfusion. THP administration reduced the inflammatory response, oxidative stress, and apoptosis in addition to inhibiting autophagy via the PI3K/AKT/mTOR pathway. Rapamycin partially reversed these effects.

Conclusion: THP promotes skin flap survival via the PI3K/AKT signaling pathway.

Keywords: Autophagy; HIF-1α; PI3K/AKT/mTOR; Skin flap survival; Tetrahydropalmatine.

MeSH terms

  • Animals
  • Berberine Alkaloids*
  • Necrosis
  • Pain
  • Phosphatidylinositol 3-Kinases* / metabolism
  • Proto-Oncogene Proteins c-akt* / metabolism
  • Rats
  • Signal Transduction
  • Sirolimus / pharmacology
  • TOR Serine-Threonine Kinases / metabolism
  • Tumor Necrosis Factor-alpha / pharmacology
  • Vascular Endothelial Growth Factor A / metabolism

Substances

  • Proto-Oncogene Proteins c-akt
  • Phosphatidylinositol 3-Kinases
  • tetrahydropalmatine
  • Vascular Endothelial Growth Factor A
  • TOR Serine-Threonine Kinases
  • Tumor Necrosis Factor-alpha
  • Sirolimus
  • Berberine Alkaloids