Styrax camporum, a typical species of the Brazilian cerrado, attenuates DNA damage, preneoplastic lesions and oxidative stress in experimental rat colon carcinogenesis

J Toxicol Environ Health A. 2021 Jul 18;84(14):582-592. doi: 10.1080/15287394.2021.1910090. Epub 2021 Apr 7.

Abstract

Styrax camporum Pohl, a typical species from the Brazilian cerrado, commonly known as "benjoeiro", is used to treat gastroduodenal diseases. In previous studies carried out by our research group, hydroalcoholic extract of S. camporum stems (SCHE) exhibited antigenotoxic and antiproliferative effects. For a comparative analysis of the chemopreventive effect of SCHE, the aim of this study was to investigate the influence of SCHE against carcinogen 1,2-dimethylhydrazine (DMH)-induced DNA damage and pre-neoplastic lesions in Wistar rat colon. Animals were treated orally with SCHE at 250, 500 or 1000 mg/kg body weight in conjunction with a subcutaneous injection of DMH. DNA damage was assessed using the comet assay while tpre-neoplastic lesions by aberrant crypt foci (ACF) assay. The following hepatic oxidative stress markers were determined including activities of catalase (CAT) and glutathione S-transferase (GST) as well as levels of reduced glutathione (GSH) and malondialdehyde (MDA). Treatment with SCHE was not genotoxic or carcinogenic at the highest dose tested (1000 mg/kg b.w.). The extract effectively inhibited DNA damage and pre-neoplastic lesions induced by DMH administration at all concentrations tested. Measurement of CAT, and GST activities and levels of GSH showed that SCHE did not reduce oxidative processes. In contrast, treatment with SCHE (1000 mg/kg b.w.) decreased liver MDA levels. Taken together, these findings suggested the chemopreventive effect attributed to SCHE in colon carcinogenesis, may be related to its capacity to inhibit DNA damage as well as an antioxidant action associated with its chemical constituents egonol and homoegonol.

Keywords: Styrax camporum; aberrant crypt foci; chemoprevention; comet assay; oxidative stress.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anticarcinogenic Agents / pharmacology*
  • Carcinogens / pharmacology
  • Carcinogens / toxicity
  • Colonic Neoplasms / drug therapy
  • Colonic Neoplasms / pathology
  • Comet Assay
  • DNA Damage / drug effects*
  • Dimethylhydrazines / pharmacology
  • Dimethylhydrazines / toxicity
  • Male
  • Oxidative Stress / drug effects*
  • Plant Extracts / chemistry
  • Plant Extracts / pharmacology*
  • Plant Stems / chemistry
  • Protective Agents / chemistry
  • Protective Agents / pharmacology*
  • Rats
  • Rats, Wistar
  • Styrax / chemistry*

Substances

  • Anticarcinogenic Agents
  • Carcinogens
  • Dimethylhydrazines
  • Plant Extracts
  • Protective Agents