Effect of verbascoside against acute kidney injury induced by rhabdomyolysis in rats

Naunyn Schmiedebergs Arch Pharmacol. 2024 Oct;397(10):7939-7950. doi: 10.1007/s00210-024-03144-1. Epub 2024 May 16.

Abstract

Rhabdomyolysis is a pathological condition caused by muscle tissue degradation. In this condition, intracellular contents enter the bloodstream, and acute kidney injury (AKI) develops. Verbascoside (VB) is one of the most common phenylethanoid glycosides and has antioxidant and anti-inflammatory effects. This study investigated the effects of VB on AKI induced by rhabdomyolysis in rats. Male Wistar rats were divided into six groups (n = 6): (1) control group (normal saline), (2) 50% glycerol (10 ml/kg, IM, single injection, only on the first day), (3)-(5) 50% glycerol (same as group 2) + VB (30, 60, and 100 mg/kg, IP, 4 days), and (6) VB (100 mg/kg). Serum and kidney tissue samples were collected on day 5. Subsequently, serum creatinine (Cr), blood urea nitrogen (BUN), renal glutathione (GSH), malondialdehyde (MDA), lipocalin associated with neutrophil gelatinase (NGAL), tumor necrosis factor-alpha (TNF-α), and pathological changes were investigated. The injection of glycerol elevated levels of kidney damage markers, including Cr and BUN in serum, MDA, TNF-α, and NGAL, along with a reduction in GSH levels in the kidney tissue. The administration of VB (100 mg/kg) significantly lowered the levels of these markers, indicating the therapeutic effect of VB against AKI caused by rhabdomyolysis. Histopathological examinations revealed enhanced myoglobin cast formation and tubular necrosis in the glycerol group, which was reduced in rats that received VB, although this reduction did not reach statistical significance. VB can reduce rhabdomyolysis-induced AKI through its anti-inflammatory and antioxidant effects and decrease kidney damage severity.

Keywords: Acute kidney injury; Anti-inflammation; Antioxidant; Oxidative stress; Verbascoside.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Kidney Injury* / drug therapy
  • Acute Kidney Injury* / metabolism
  • Acute Kidney Injury* / pathology
  • Acute Kidney Injury* / prevention & control
  • Acute-Phase Proteins / metabolism
  • Animals
  • Anti-Inflammatory Agents / pharmacology
  • Antioxidants* / pharmacology
  • Blood Urea Nitrogen
  • Creatinine / blood
  • Glucosides* / pharmacology
  • Glucosides* / therapeutic use
  • Glutathione / metabolism
  • Kidney / drug effects
  • Kidney / metabolism
  • Kidney / pathology
  • Lipocalin-2
  • Lipocalins
  • Male
  • Malondialdehyde / metabolism
  • Oxidative Stress / drug effects
  • Phenols* / pharmacology
  • Polyphenols
  • Rats
  • Rats, Wistar*
  • Rhabdomyolysis* / chemically induced
  • Rhabdomyolysis* / complications
  • Rhabdomyolysis* / drug therapy
  • Tumor Necrosis Factor-alpha* / blood
  • Tumor Necrosis Factor-alpha* / metabolism

Substances

  • acteoside
  • Glucosides
  • Phenols
  • Antioxidants
  • Tumor Necrosis Factor-alpha
  • Lipocalin-2
  • Malondialdehyde
  • Glutathione
  • Lcn2 protein, rat
  • Creatinine
  • Anti-Inflammatory Agents
  • Lipocalins
  • Acute-Phase Proteins
  • Polyphenols