The α-1 Adrenergic Receptor Antagonist Doxazosin Attenuates Liver Fibrosis by Alleviating Sinusoidal Capillarization and Liver Angiogenesis

Adv Biol (Weinh). 2024 Jun;8(6):e2300513. doi: 10.1002/adbi.202300513. Epub 2024 Mar 17.

Abstract

Liver fibrosis and cirrhosis, which are caused by chronic liver injury, represent common and intractable clinical challenges of global importance. However, effective therapeutics are lacking. Therefore, the study examines the effect of doxazosin on liver fibrosis. Carbon tetrachloride (CCl4) is injected into mice to establish a liver fibrosis model. Doxazosin (5 and 10 mg/kg) is administered daily by gavage. HE staining, Masson staining, Sirius Red staining, scanning electron microscopy, western blotting, real-time PCR, and immunofluorescence analysis are performed to estimate liver fibrosis and sinusoidal capillarization in mice. Cell Counting Kit-8 assays, western blotting, immunofluorescence analysis, tube formation, and transwell migration assays are performed on human umbilical vein endothelial cells (HUVECs) and human hepatic sinusoidal endothelial cells (HHSECs) to elucidate the potential mechanism of doxazosin. Doxazosin alleviates liver fibrosis and sinusoidal capillarization in CCl4-induced mice. Angiogenesis is attenuated by doxazosin in HUVECs and HHSECs. This study demonstrates that doxazosin attenuated liver fibrosis by alleviating sinusoidal capillarization and liver angiogenesis.

Keywords: angiogenesis; doxazosin; hepatic sinusoidal endothelial cell; liver fibrosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic alpha-1 Receptor Antagonists* / pharmacology
  • Adrenergic alpha-1 Receptor Antagonists* / therapeutic use
  • Angiogenesis
  • Animals
  • Capillaries / drug effects
  • Capillaries / pathology
  • Carbon Tetrachloride / toxicity
  • Disease Models, Animal
  • Doxazosin* / pharmacology
  • Doxazosin* / therapeutic use
  • Human Umbilical Vein Endothelial Cells* / drug effects
  • Humans
  • Liver Cirrhosis* / drug therapy
  • Liver Cirrhosis* / pathology
  • Liver* / blood supply
  • Liver* / drug effects
  • Liver* / pathology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Neovascularization, Pathologic* / drug therapy
  • Neovascularization, Pathologic* / pathology

Substances

  • Doxazosin
  • Adrenergic alpha-1 Receptor Antagonists
  • Carbon Tetrachloride