NAC attenuates adriamycin-induced nephrotic syndrome in rats through regulating TLR4 signaling pathway

Eur Rev Med Pharmacol Sci. 2017 Apr;21(8):1938-1943.

Abstract

Objective: Nephrotic syndrome (NS) is a detrimental renal disease that affects a large population. It is suggested that Toll-like Receptor 4 (TLR4) signaling pathway plays an important role in NS. The aim of this study was to evaluate the immunosuppressive effect of N-acetylcysteine (NAC) in the treatment of NS elucidate its interaction with TLR4 pathway in a rat model.

Materials and methods: Rat NS model was constructed using the Bertain method by injecting adriamycin (4.5 mg/kg) intravenously at day 1, and injecting 2 mg/kg adriamycin (ADR) at day 7. NS rats were treatment with NAC of 150 mg/kg daily through gavage. Control rats received equivalent amounts of saline daily. Quantitative Real-time PCR was used to evaluate TLR4 expression in kidney tissues after treatments. Western blot analysis was used to evaluate NF-κBp65 expression. ELISA was used to evaluate the expression of immunological factors, including TNF-α, IL-6, and IL-1β.

Results: Rat NS models demonstrated higher protein levels in urine, accompanied by an increased in the TLR4 level. After NAC treatment, TLR4 level was reduced. NAC treatment also attenuated the NF-κBp65 overexpression in NS rats. Concomitantly, TNF-α, IL-6, and IL-1β levels, which are indicators of immunological and informatory responses, were also decreased after NAC treatment.

Conclusions: NAC treatment ameliorated nephrotic syndrome in NS rat models by suppressing TLR4 signaling, as well as immunological and inflammatory responses.

MeSH terms

  • Acetylcysteine / pharmacology*
  • Animals
  • Cytokines / analysis
  • Doxorubicin / toxicity*
  • Male
  • NF-kappa B / analysis
  • Nephrotic Syndrome / chemically induced
  • Nephrotic Syndrome / drug therapy*
  • Nephrotic Syndrome / immunology
  • Proteinuria / drug therapy
  • Rats
  • Rats, Wistar
  • Signal Transduction / drug effects*
  • Toll-Like Receptor 4 / physiology*

Substances

  • Cytokines
  • NF-kappa B
  • Tlr4 protein, rat
  • Toll-Like Receptor 4
  • Doxorubicin
  • Acetylcysteine