Cocoplum (Chrysobalanus icaco L.) decreases doxorubicin-induced DNA damage and downregulates Gadd45a, Il-1β, and Tnf-α in vivo

Food Res Int. 2018 Mar:105:996-1002. doi: 10.1016/j.foodres.2017.12.009. Epub 2017 Dec 6.

Abstract

DNA damage and inflammation are promising targets in disease prevention studies. Since these pathways have shown to be modulated by dietary components, investigating the molecular effects of food becomes relevant. This study aimed at investigating the protective effects of cocoplum (Chrysobalanus icaco L.) against doxorubicin (DXR)-induced damage. Rats were treated with cocoplum (100, 200 or 400mg/kg/day) for 14days, associated or not with DXR (15mg/kg b.w.). Tissue-targeted comet assay and the oxidative stress parameters oxidized/reduced glutathione and catalase were investigated in liver, kidney, and heart. The expressions of DNA damage/repair (Gadd45a, Parp1, Xrcc2) and proinflammatory genes (Il-1β, Il-6, Nf-κb, Tnf-α) were performed by real-time quantitative PCR. Cocoplum decreased DNA damage and the expressions of Gadd45a, Il-1β, and Tnf-α induced by DXR. These findings demonstrate that cocoplum fruits possess antigenotoxic and anti-inflammatory effects against DXR-induced damage and encourage other in vivo/clinical studies with this fruit.

Keywords: Chrysobalanus icaco; Comet assay; Genotoxicity; In vivo; Inflammation; Phytochemicals.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / isolation & purification
  • Anti-Inflammatory Agents / pharmacology*
  • Antimutagenic Agents / isolation & purification
  • Antimutagenic Agents / pharmacology*
  • Catalase / metabolism
  • Cell Cycle Proteins / genetics
  • Cell Cycle Proteins / metabolism*
  • Chrysobalanaceae / chemistry*
  • Comet Assay
  • DNA Damage / drug effects*
  • Down-Regulation
  • Doxorubicin / toxicity*
  • Glutathione / metabolism
  • Interleukin-1beta / genetics
  • Interleukin-1beta / metabolism*
  • Kidney / drug effects
  • Kidney / metabolism
  • Liver / drug effects
  • Liver / metabolism
  • Male
  • Myocytes, Cardiac / drug effects
  • Myocytes, Cardiac / metabolism
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism*
  • Oxidation-Reduction
  • Oxidative Stress / drug effects
  • Plant Extracts / isolation & purification
  • Plant Extracts / pharmacology*
  • Rats, Wistar
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / metabolism*

Substances

  • Anti-Inflammatory Agents
  • Antimutagenic Agents
  • Cell Cycle Proteins
  • Gadd45a protein, rat
  • IL1B protein, rat
  • Interleukin-1beta
  • Nuclear Proteins
  • Plant Extracts
  • Tumor Necrosis Factor-alpha
  • Doxorubicin
  • Catalase
  • Glutathione