ROCK1 inhibition improves wound healing in diabetes via RIPK4/AMPK pathway

Acta Pharmacol Sin. 2024 Jul;45(7):1477-1491. doi: 10.1038/s41401-024-01246-3. Epub 2024 Mar 27.

Abstract

Refractory wounds are a severe complication of diabetes mellitus that often leads to amputation because of the lack of effective treatments and therapeutic targets. The pathogenesis of refractory wounds is complex, involving many types of cells. Rho-associated protein kinase-1 (ROCK1) phosphorylates a series of substrates that trigger downstream signaling pathways, affecting multiple cellular processes, including cell migration, communication, and proliferation. The present study investigated the role of ROCK1 in diabetic wound healing and molecular mechanisms. Our results showed that ROCK1 expression significantly increased in wound granulation tissues in diabetic patients, streptozotocin (STZ)-induced diabetic mice, and db/db diabetic mice. Wound healing and blood perfusion were dose-dependently improved by the ROCK1 inhibitor fasudil in diabetic mice. In endothelial cells, fasudil and ROCK1 siRNA significantly elevated the phosphorylation of adenosine monophosphate-activated protein kinase at Thr172 (pThr172-AMPKα), the activity of endothelial nitric oxide synthase (eNOS), and suppressed the levels of mitochondrial reactive oxygen species (mtROS) and nitrotyrosine formation. Experiments using integrated bioinformatics analysis and coimmunoprecipitation established that ROCK1 inhibited pThr172-AMPKα by binding to receptor-interacting serine/threonine kinase 4 (RIPK4). These results suggest that fasudil accelerated wound repair and improved angiogenesis at least partially through the ROCK1/RIPK4/AMPK pathway. Fasudil may be a potential treatment for refractory wounds in diabetic patients.

Keywords: AMPK; ROCK1; diabetes; mitochondria; wound.

MeSH terms

  • 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine* / analogs & derivatives
  • 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine* / pharmacology
  • 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine* / therapeutic use
  • AMP-Activated Protein Kinases / metabolism
  • Animals
  • Diabetes Mellitus, Experimental* / metabolism
  • Female
  • Human Umbilical Vein Endothelial Cells
  • Humans
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Nitric Oxide Synthase Type III / metabolism
  • Protein Kinase Inhibitors / pharmacology
  • Protein Kinase Inhibitors / therapeutic use
  • Protein Serine-Threonine Kinases / antagonists & inhibitors
  • Protein Serine-Threonine Kinases / metabolism
  • Signal Transduction* / drug effects
  • Wound Healing* / drug effects
  • rho-Associated Kinases* / antagonists & inhibitors
  • rho-Associated Kinases* / metabolism

Substances

  • rho-Associated Kinases
  • 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine
  • fasudil
  • ROCK1 protein, human
  • AMP-Activated Protein Kinases
  • Rock1 protein, mouse
  • Protein Kinase Inhibitors
  • Protein Serine-Threonine Kinases
  • Nitric Oxide Synthase Type III