Diagnosis, toxicological mechanism, and detoxification for hepatotoxicity induced by pyrrolizidine alkaloids from herbal medicines or other plants

Crit Rev Toxicol. 2024 Feb;54(2):123-133. doi: 10.1080/10408444.2024.2310597. Epub 2024 Feb 27.

Abstract

Pyrrolizidine alkaloids (PAs) are one type of phytotoxins distributed in various plants, including many medicinal herbs. Many organs might suffer injuries from the intake of PAs, and the liver is the most susceptible one. The diagnosis, toxicological mechanism, and detoxification of PAs-induced hepatotoxicity have been studied for several decades, which is of great significance for its prevention, diagnosis, and therapy. When the liver was exposed to PAs, liver sinusoidal endothelial cells (LSECs) loss, hemorrhage, liver parenchymal cells death, nodular regeneration, Kupffer cells activation, and fibrogenesis occurred. These pathological changes classified the PAs-induced liver injury as acute, sub-acute, and chronic type. PAs metabolic activation, mitochondria injury, glutathione (GSH) depletion, inflammation, and LSECs damage-induced activation of the coagulation system were well recognized to play critical roles in the pathological process of PAs-induced hepatotoxicity. A lot of natural compounds like glycyrrhizic acid, (-)-epicatechin, quercetin, baicalein, chlorogenic acid, and so on were demonstrated to be effective in alleviating PAs-induced liver injury, which rendered them huge potential to be developed into therapeutic drugs for PAs poisoning in clinics. This review presents updated information about the diagnosis, toxicological mechanism, and detoxification studies on PAs-induced hepatotoxicity.

Keywords: Pyrrolizidine alkaloids; detoxification; diagnosis; hepatotoxicity; toxicological mechanism.

Publication types

  • Review

MeSH terms

  • Chemical and Drug Induced Liver Injury, Chronic* / pathology
  • Endothelial Cells / metabolism
  • Endothelial Cells / pathology
  • Glutathione / metabolism
  • Plant Extracts
  • Plants, Medicinal* / metabolism
  • Pyrrolizidine Alkaloids* / metabolism
  • Pyrrolizidine Alkaloids* / toxicity

Substances

  • Pyrrolizidine Alkaloids
  • Glutathione
  • Plant Extracts