Peroxisomicine A1 (toxin T-514) induces cell death of hepatocytes in vivo by triggering the intrinsic apoptotic pathway

Toxicon. 2018 Nov:154:79-89. doi: 10.1016/j.toxicon.2018.09.010. Epub 2018 Sep 28.

Abstract

Karwinskia parvifolia possesses the highest concentration levels of the anthracenone T-514 (PA1). Studies have demonstrated the induction of apoptosis by PA1 in cancer cell lines. The aim was to investigate the effects of PA1 on the apoptosis of the mouse liver in vivo and its underlying pathway. Sixty CD-1 mice were divided into three groups: untreated, vehicle, and treated with PA1. The animals were euthanized at 4, 8, 12, and 24 h post-treatment. To confirm the toxic effect of PA1 we determined the activity of catalase. Liver sections were prepared for morphological examination and for immunohistochemical evaluation of anti and pro-apoptotic markers. DNA fragmentation was detected by TUNEL assay and electrophoresis. Pre-apoptotic mitochondrial alterations and cytochrome c oxidase activity were analyzed by transmission electron microscopy. PA1 induced pre-apoptotic mitochondrial alterations, a high activity of the cytochrome oxidase, and apoptosis in hepatocytes. PA1 caused p53 over-expression and down regulation of PCNA. PA1 also increased the expression levels of the pro-apoptotic markers Bax and Bak, whereas the anti-apoptotic molecule Bcl-2 was decreased. PA1 induces apoptosis by activating the intrinsic mitochondrial apoptotic pathway. These results will be useful for studies regarding the use of PA1 as an antineoplastic agent.

Keywords: Apoptosis; Liver; Peroxisomicine A1; Plant toxin; T-514.

MeSH terms

  • Animals
  • Anthracenes / isolation & purification
  • Anthracenes / pharmacology*
  • Anthracenes / toxicity
  • Apoptosis / drug effects*
  • Apoptosis Regulatory Proteins / metabolism
  • Caspase 3 / metabolism
  • Catalase / metabolism
  • Cytochromes c / metabolism
  • Hepatocytes / drug effects*
  • Hepatocytes / metabolism
  • Hepatocytes / pathology
  • Mice
  • Mitochondria / metabolism
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Signal Transduction / drug effects
  • bcl-2-Associated X Protein / metabolism

Substances

  • Anthracenes
  • Apoptosis Regulatory Proteins
  • Proto-Oncogene Proteins c-bcl-2
  • bcl-2-Associated X Protein
  • Karwinskia toxin T-514
  • Cytochromes c
  • Catalase
  • Caspase 3