Alleviative Effect of Lactoferrin Interventions Against the Hepatotoxicity Induced by Titanium Dioxide Nanoparticles

Biol Trace Elem Res. 2024 Feb;202(2):624-642. doi: 10.1007/s12011-023-03702-3. Epub 2023 May 16.

Abstract

The current study was designed to investigate the alleviative effect of lactoferrin interventions against the hepatotoxicity induced by titanium dioxide nanoparticles (TiO2-NPs). Thirty male Wistar rats were divided into six groups with 5 rats in each group. The first and second groups were intragastrically administered normal saline and TiO2-NPs (100 mg/kg body weight) as the negative control (NC) and TiO2-NP groups. The third, fourth, and fifth groups were intragastrically administered lactoferrin at concentrations of 100, 200, and 400 mg/kg body weight in addition to TiO2-NPs (100 mg/kg body weight). The sixth group was intragastrically administered Fuzheng Huayu (FZHY) capsules at a concentration of 4.6 g/kg body weight in addition to TiO2-NPs (100 mg/kg body weight) as the positive control group. After treatment for 4 weeks, the concentrations of lactoferrin were optimized based on the liver index and function results. Subsequently, the alleviative effects of lactoferrin interventions against TiO2-NP-induced hepatotoxicity in rat liver tissues, including the effects on histological damage, oxidative stress-related damage, inflammation, fibrosis, DNA damage, apoptosis, and gene expression, were investigated using histopathological, biochemical, and transcriptomic assays. The results showed that 200 mg/kg lactoferrin interventions for 4 weeks not only ameliorated the liver dysfunction and histopathological damage caused by TiO2-NP exposure but also inhibited the oxidative stress-related damage, inflammation, fibrosis, DNA damage, and apoptosis in the liver tissues of TiO2-NP-exposed rats. The transcriptomic results confirmed that the alleviative effect of lactoferrin interventions against the TiO2-NP exposure-induced hepatotoxicity was related to the activation of the PI3K/AKT signaling pathway.

Keywords: Hepatotoxicity; Lactoferrin; Oxidative stress; PI3K/AKT; Titanium dioxide nanoparticles.

MeSH terms

  • Animals
  • Body Weight
  • Chemical and Drug Induced Liver Injury* / prevention & control
  • Fibrosis
  • Inflammation
  • Lactoferrin / pharmacology
  • Male
  • Metal Nanoparticles* / toxicity
  • Nanoparticles* / toxicity
  • Oxidative Stress
  • Phosphatidylinositol 3-Kinases
  • Rats
  • Rats, Wistar
  • Titanium / toxicity

Substances

  • titanium dioxide
  • Lactoferrin
  • Phosphatidylinositol 3-Kinases
  • Titanium