Effect of protein malnutrition on the metabolism and toxicity of cisplatin, 5-fluorouracil and mitomycin C in rat stomach

Food Chem Toxicol. 2013 Jun:56:467-82. doi: 10.1016/j.fct.2013.02.042. Epub 2013 Feb 28.

Abstract

This study investigated the effect of protein malnutrition on metabolism and toxicity of cisplatin (CP), 5-fluorouracil (FU) and mitomycin C (MMC) in rat stomach. Weanling male Wistar rats received a normal (24%) or low (2.5%) protein diet for 28 days and were allocated into: normally-fed control, protein-malnourished control (PM), 3 normally-fed drug-treated groups and 3 protein-malnourished drug-treated groups (PM-CP, PM-FU and PM-MMC). Cisplatin and MMC were injected intraperitoneally (8 mg/kg on day 26 and 1 mg/kg/day for 7 days, respectively). 5-Fluorouracil was given orally (50 mg/kg/day for 5 days). Compared with normally-fed counterparts, PM-CP rats exhibited higher glutathione S-transferase, aminopeptidase N and cysteine S-conjugate beta-lyase (CCBL) and lower gamma-glutamyltransferase activities, PM-FU rats exhibited decreased dihydropyrimidine dehydrogenase and cytochrome P450 1A1/2 activities and PM-MMC rats showed higher quinone reductase and depleted xanthine oxidase activities. Protein-malnourished drug-treated groups exhibited exacerbated gastrotoxicity, relative to normally-fed counterparts, manifested by lower mucus levels, higher permeability and histopathological deterioration, along with increased oxidative stress in PM-CP rats and exaggerated prostaglandin E2 production in PM-MMC rats. Conclusively, protein malnutrition alters CP, FU and MMC metabolism in rat stomach by enhancing CCBL pathway for CP activation, delaying FU elimination and activating two-electron reduction of MMC, potentiating their gastrotoxicity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carbon-Sulfur Lyases / metabolism
  • Cisplatin / administration & dosage
  • Cisplatin / toxicity*
  • Cytochrome P-450 CYP1A1 / metabolism
  • Cytochrome P-450 CYP1A2 / metabolism
  • Dihydrouracil Dehydrogenase (NADP) / metabolism
  • Fluorouracil / administration & dosage
  • Fluorouracil / toxicity*
  • Gastric Mucosa / metabolism
  • Glutathione Transferase / metabolism
  • Male
  • Mitomycin / administration & dosage
  • Mitomycin / toxicity*
  • NAD(P)H Dehydrogenase (Quinone) / metabolism
  • Protein-Energy Malnutrition / chemically induced
  • Protein-Energy Malnutrition / pathology*
  • Rats
  • Rats, Wistar
  • Stomach / drug effects*
  • Xanthine Oxidase / metabolism
  • gamma-Glutamyltransferase / metabolism

Substances

  • Mitomycin
  • Cytochrome P-450 CYP1A1
  • Cytochrome P-450 CYP1A2
  • Xanthine Oxidase
  • Dihydrouracil Dehydrogenase (NADP)
  • NAD(P)H Dehydrogenase (Quinone)
  • gamma-Glutamyltransferase
  • Glutathione Transferase
  • Carbon-Sulfur Lyases
  • cysteine-S-conjugate beta-lyase
  • Cisplatin
  • Fluorouracil