[Subacute toxicity metabonomics of Jinlingzi powder based on LC-MS]

Shu-Jie Shen1, Su-Fang Shui2, Bing-Kun Xiao1

  • 1Beijing Institute of Radiation Medicine, Beijing 100850, China.

Insights

Jinlingzi powder causes dose-dependent toxicity in rats, impacting liver and kidney function. Key metabolic pathways like lysine and glutathione metabolism are disrupted, leading to energy imbalance and oxidative stress.

Area of Science:

  • Toxicology
  • Metabolomics
  • Pharmacology

Background:

  • Jinlingzi powder's metabolic effects and toxicity mechanisms require further investigation.
  • Understanding its impact on biological pathways is crucial for assessing its safety.

Purpose of the Study:

  • To elucidate the metabolic characteristics of Jinlingzi powder toxicity in rats.
  • To explore the influence of Jinlingzi powder on unknown biological pathways during treatment.

Main Methods:

  • LC-MS analysis of rat urine and serum samples.
  • XCMS online analysis for metabolite identification.
  • Metpa for metabolic pathway enrichment and network analysis.

Main Results:

  • Identified 44 differential metabolites and five key metabolic pathways: steroid hormone biosynthesis, tryptophan metabolism, pentose and glucuronate interconversions, ascorbate and aldarate metabolism, and glutathione metabolism.
  • Disruptions in lysine, glucuronic acid, and hormone metabolism were linked to toxicity.
  • Lysine and glutathione metabolism imbalance correlated with energy metabolism disorders and oxidative stress.

Conclusions:

  • Jinlingzi powder exhibits dose-dependent toxicity in rats, with significant effects observed at 19.7 g•kg⁻¹ and 39.4 g•kg⁻¹.
  • Metabolic pathway alterations, particularly in lysine and glutathione metabolism, contribute to Jinlingzi powder-induced toxicity and potential irreversible organ damage.

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