Effects of Pemafibrate on Reducing Oxidative Stress and Augmenting Angiogenesis in Ischemic Limb Tissue

Kurume Med J. 2024 May 14;69(3.4):167-174. doi: 10.2739/kurumemedj.MS6934006. Epub 2024 Jan 16.

Abstract

Objective: Oxidative damage is observed in the ischemic limbs of patients with arteriosclerosis obliterans. We investigated whether pemafibrate, a selective peroxisome proliferator-activated receptor alpha modulator, reduced oxidative stress in ischemic limbs and consequently rescued limb damage in model mice.

Materials and methods: We surgically induced hind-limb ischemia in mice and orally administered pemafibrate solution (P-05 group, 0.5 mg/kg/day; P-10 group, 1.0 mg/kg/day) or control solution (control group). Seven days after the surgery, differences in reactive oxygen species (ROS) contents, antioxidative enzyme and transcription factor expression, blood flow, and capillary density in ischemic limbs were assessed.

Results: Tissue ROS levels were lower in the P-05 and P-10 groups compared with those in the control group. Although the tissue expression levels of nuclear factor-erythroid 2-related factor 2 increased in the P-10 group compared with that in the control group, no corresponding changes were observed in the tissue expression of four antioxidative enzymes. The limb salvage rates and capillary densities in ischemic limbs were higher in the P-05 and P-10 groups than that in the control group.

Conclusion: Pemafibrate treatment reduced oxidative stress and augmented angiogenesis in ischemic limbs, contributing to prevention of limb damage in mice.

Keywords: antioxidant; arteriosclerosis obliterans; limb salvage; necrosis; pemafibrate.

MeSH terms

  • Angiogenesis
  • Animals
  • Antioxidants / pharmacology
  • Benzoxazoles* / pharmacology
  • Benzoxazoles* / therapeutic use
  • Butyrates* / pharmacology
  • Butyrates* / therapeutic use
  • Disease Models, Animal*
  • Hindlimb* / blood supply
  • Ischemia* / drug therapy
  • Ischemia* / metabolism
  • Limb Salvage
  • Male
  • Mice
  • NF-E2-Related Factor 2 / metabolism
  • Neovascularization, Physiologic* / drug effects
  • Oxidative Stress* / drug effects
  • PPAR alpha / metabolism
  • Reactive Oxygen Species* / metabolism
  • Regional Blood Flow / drug effects