Enhancing the efficacy of low doses of N-acetyl-L-cysteine in mitigating CCl4-induced hepatotoxicity in animal model using physical cold plasma

Ecotoxicol Environ Saf. 2025 Jan 1:289:117642. doi: 10.1016/j.ecoenv.2024.117642. Epub 2025 Jan 6.

Abstract

Liver diseases have become widespread especially due to various factors of modern life. Although the effect of N-acetyl-L-cysteine (NAC) is investigated in the recovery of liver damage, gas plasma therapy can be identified as a promising candidate. Our study aimed to enhance the effectiveness of ineffective doses of NAC in stopping CCl4-induced hepatotoxicity in rats by physical cold plasma. The plasma-treated NAC (PTN) structural changes were investigated through FTIR and LCMS/MS analysis. It was observed that the PTN consists of various chemical bioproducts with different molecular weights. We investigated an ineffective dose of NAC and its parallel effect through the administration of PTN on liver and kidney morphology and several biochemical factors including ALT, AST, and ALP. Additionally, we examined oxidative stress, antioxidant parameters, and glutathione (GSH) levels. Results showed that PTN exhibited greater antioxidant properties and increased GSH levels, contributing to its therapeutic effects. Also, the antioxidant enzymes and oxidative stress activities improved after receiving PTN. It also enhanced histological parameters, although various damages were detected in both liver and kidney tissues after CCl4 injection, PTN remarkably prevented the tissue changes caused by CCl4. PTN could protect against liver damage even at a very low dose of NAC, acting as a prophylactic drug with a high margin of safety for hepatotoxicity.

Keywords: CCl(4)-induced hepatotoxicity; Cold atmospheric pressure plasma; N-acetyl-L-cysteine; Reactive oxygen and nitrogen species.

MeSH terms

  • Acetylcysteine* / pharmacology
  • Animals
  • Antioxidants*
  • Carbon Tetrachloride* / toxicity
  • Chemical and Drug Induced Liver Injury* / prevention & control
  • Disease Models, Animal
  • Glutathione / metabolism
  • Kidney / drug effects
  • Kidney / pathology
  • Liver* / drug effects
  • Liver* / pathology
  • Male
  • Oxidative Stress* / drug effects
  • Plasma Gases*
  • Rats
  • Rats, Sprague-Dawley
  • Rats, Wistar

Substances

  • Acetylcysteine
  • Carbon Tetrachloride
  • Plasma Gases
  • Antioxidants
  • Glutathione