Insights into the effects of chronic combined chromium-nickel exposure on colon damage in mice through transcriptomic analysis and in vitro gastrointestinal digestion assay

Ecotoxicol Environ Saf. 2024 Jul 1:279:116458. doi: 10.1016/j.ecoenv.2024.116458. Epub 2024 May 17.

Abstract

Heavy metals interact with each other in a coexisting manner to produce complex combined toxicity to organisms. At present, the toxic effects of chronic co-exposure to heavy metals hexavalent chromium [Cr(VI)] and divalent nickel [Ni(II)] on organisms are seldom studied and the related mechanisms are poorly understood. In this study, we explored the mechanism of the colon injury in mice caused by chronic exposure to Cr or/and Ni. The results showed that, compared with the control group, Cr or/and Ni chronic exposure affected the body weight of mice, and led to infiltration of inflammatory cells in the colon, decreased the number of goblet cells, fusion of intracellular mucus particles and damaged cell structure of intestinal epithelial. In the Cr or/and Ni exposure group, the activity of nitric oxide synthase (iNOS) increased, the expression levels of MUC2 were significantly down-regulated, and those of ZO-1 and Occludin were significantly up-regulated. Interestingly, factorial analysis revealed an interaction between Cr and Ni, which was manifested as antagonistic effects on iNOS activity, ZO-1 and MUC2 mRNA expression levels. Transcriptome sequencing further revealed that the expression of genes-related to inflammation, intestinal mucus and tight junctions changed obviously. Moreover, the relative contents of Cr(VI) and Ni(II) in the Cr, Ni and Cr+Ni groups all changed with in-vitro gastrointestinal (IVG)digestion, especially in the Cr+Ni group. Our results indicated that the chronic exposure to Cr or/and Ni can lead to damage to the mice colon, and the relative content changes of Cr(VI) and Ni(II) might be the main reason for the antagonistic effect of Cr+Ni exposure on the colon damage.

Keywords: Goblet cell; In vitro gastrointestinal digestion; Intestinal inflammation; RNA-seq; Tight junction.

MeSH terms

  • Animals
  • Chromium* / toxicity
  • Colon* / drug effects
  • Colon* / pathology
  • Digestion / drug effects
  • Gene Expression Profiling
  • Intestinal Mucosa / drug effects
  • Intestinal Mucosa / metabolism
  • Intestinal Mucosa / pathology
  • Male
  • Mice
  • Mucin-2* / genetics
  • Mucin-2* / metabolism
  • Nickel* / toxicity
  • Nitric Oxide Synthase Type II / genetics
  • Nitric Oxide Synthase Type II / metabolism
  • Occludin / genetics
  • Occludin / metabolism
  • Transcriptome / drug effects
  • Zonula Occludens-1 Protein / genetics
  • Zonula Occludens-1 Protein / metabolism

Substances

  • Chromium
  • Nickel
  • Mucin-2
  • Nitric Oxide Synthase Type II
  • Muc2 protein, mouse
  • chromium hexavalent ion
  • Nos2 protein, mouse
  • Zonula Occludens-1 Protein
  • Occludin
  • Tjp1 protein, mouse