The long persistence of pyrrolizidine alkaloid-derived pyrrole-protein adducts in vivo: Kinetic study following multiple exposures of a pyrrolizidine alkaloid containing extract of Gynura japonica

Toxicol Lett. 2020 May 1:323:41-47. doi: 10.1016/j.toxlet.2020.01.021. Epub 2020 Jan 23.

Abstract

Gynura japonica (also named Tusanqi in Chinese) is used as a folk herbal medicine for treating blood stasis or traumatic injury. However, hundreds of hepatic sinusoidal obstruction syndrome (HSOS) cases have been reported after consumption of preparations made from G. japonica because it contains large amounts of hepatotoxic pyrrolizidine alkaloids (PAs). To date, blood pyrrole-protein adducts (PPAs) are suggested as biomarkers for the diagnosis of PA-induced HSOS in clinics. However, the concentration of PPAs in the blood is greatly affected by several factors including the amount of PA exposure, herb intake period, and blood sampling time after the last exposure. In present study, the kinetic characters of PPAs in serum and liver as well as other potential target organs were studied systematically and comprehensively following multiple exposures of PAs in G. japonica extract (GJE). As results, PPAs content reached to a plateau both in serum and liver after the mice were treated with GJE for 2 weeks on daily basis. PPAs cleared significantly slower in liver (T1/2ke∼184.6 h, ∼7.7 days) than in serum (T1/2ke∼95.8 h, ∼4.0 days). Although more than 90 % PPAs were removed 2 weeks after the last dosing, PPAs still persisted in the liver until the end of the experiment, i.e. 8 weeks after the last dosing. The results would be of great help for understanding the importance of PPAs for PA-induced toxicity and its detoxification.

Keywords: Biomarker; Gynura japonica; Hepatic sinusoidal obstruction syndrome; Kinetic study; Pyrrole-protein adducts; Pyrrolizidine alkaloids.

MeSH terms

  • Animals
  • Blood Proteins / metabolism*
  • Drugs, Chinese Herbal / pharmacokinetics*
  • Drugs, Chinese Herbal / toxicity
  • Hepatic Veno-Occlusive Disease / chemically induced*
  • Kinetics
  • Liver / drug effects
  • Liver / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Plant Extracts / analysis
  • Plant Extracts / toxicity
  • Pyrroles / metabolism*
  • Pyrrolizidine Alkaloids / pharmacokinetics*
  • Pyrrolizidine Alkaloids / toxicity

Substances

  • Blood Proteins
  • Drugs, Chinese Herbal
  • Plant Extracts
  • Pyrroles
  • Pyrrolizidine Alkaloids
  • tusanqi