Rho Kinase Inhibitor, Fasudil, Attenuates Contrast-induced Acute Kidney Injury

Basic Clin Pharmacol Toxicol. 2018 Feb;122(2):278-287. doi: 10.1111/bcpt.12895. Epub 2017 Sep 19.

Abstract

In this study, we tested the hypothesis that fasudil, a Rho kinase inhibitor, would protect against contrast-induced acute kidney injury (CI-AKI) in a mouse model and attempted to elucidate the mechanism involved. Mice subjected to unilateral ligation of the left anterior renal pedicle were divided into four groups: (1) control group, (2) CI-AKI induced by contrast media (CM group), (3) CI-AKI plus low-dose fasudil (LD group) and (4) CI-AKI plus high-dose fasudil (HD group). Animals from groups 2-4 received iodixanol (4.0 g iodine/kg), and the control group received saline. At 12, 2 hr before iodixanol injection and 4 hr after iodixanol administration, the animals in groups 3-4 received 3 or 10 mg/kg fasudil, respectively. Renal blood flow, renal function parameters, kidney histology and the expression of proteins that regulates apoptosis and inflammation were determined 24 hr later. Fasudil treatment notably ameliorated contrast medium-induced medullary damage, restored renal function, suppressed renal tubular apoptosis, ameliorated redox imbalance and DNA damage. Fasudil had a nephroprotective effect that was partially attributed to its anti-inflammatory, anti-apoptotic and antioxidant effects of inhibiting the Rho/ROCK pathway.

MeSH terms

  • 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine / analogs & derivatives*
  • 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine / pharmacology
  • Acute Kidney Injury / chemically induced
  • Acute Kidney Injury / enzymology
  • Acute Kidney Injury / pathology
  • Acute Kidney Injury / prevention & control*
  • Animals
  • Apoptosis / drug effects
  • Biomarkers / blood
  • Biomarkers / urine
  • Contrast Media*
  • Cytoprotection
  • DNA Damage / drug effects
  • Disease Models, Animal
  • Inflammation Mediators / blood
  • Kidney / drug effects*
  • Kidney / enzymology
  • Kidney / pathology
  • Male
  • Mice, Inbred BALB C
  • Oxidation-Reduction
  • Oxidative Stress / drug effects
  • Protein Kinase Inhibitors / pharmacology*
  • Renal Circulation / drug effects
  • Signal Transduction / drug effects
  • Triiodobenzoic Acids*
  • rho-Associated Kinases / antagonists & inhibitors*
  • rho-Associated Kinases / metabolism

Substances

  • Biomarkers
  • Contrast Media
  • Inflammation Mediators
  • Protein Kinase Inhibitors
  • Triiodobenzoic Acids
  • 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine
  • rho-Associated Kinases
  • iodixanol
  • fasudil