Telomere length and genotoxicity in the lung of rats following intragastric exposure to food-grade titanium dioxide and vegetable carbon particles.
A549 Cells
Animals
Caco-2 Cells
Carbon
/ toxicity
DNA Damage
/ drug effects
Epithelial Cells
/ drug effects
Female
Food Additives
/ toxicity
Humans
Intestines
/ drug effects
Lung
/ drug effects
Nanoparticles
/ toxicity
Occludin
/ genetics
Particle Size
Rats
Rats, Zucker
Reactive Oxygen Species
/ metabolism
Stomach
Telomere
/ drug effects
Tight Junctions
/ drug effects
Titanium
/ toxicity
Journal
Mutagenesis
ISSN: 1464-3804
Titre abrégé: Mutagenesis
Pays: England
ID NLM: 8707812
Informations de publication
Date de publication:
29 05 2019
29 05 2019
Historique:
received:
08
11
2018
revised:
28
01
2019
accepted:
08
02
2019
pubmed:
11
3
2019
medline:
19
5
2020
entrez:
11
3
2019
Statut:
ppublish
Résumé
Vegetable carbon (E153) and titanium dioxide (E171) are widely used as black and white food colour additives. The aim of this study was to assess gastrointestinal tight junction and systemic genotoxic effects in rats following exposure to E153 and E171 for 10 weeks by oral gavage once a week. The expression of tight junction proteins was assessed in intestinal tissues. Levels of DNA strand breaks, oxidatively damaged DNA and telomere length were assessed in secondary organs. Hydrodynamic suspensions of E153 and E173 indicated mean particles sizes of 230 and 270 nm, respectively, and only E153 gave rise to intracellular production of reactive oxygen species in colon epithelial (Caco-2) cells. Rats exposed to E153 (6.4 mg/kg/week) or E171 (500 mg/kg/week) had decreased gene expression of the tight junction protein TJP1 (P < 0.05). E153 (6.4 mg/kg/week) also decreased OCLN (P < 0.05) in the colon and occludin protein expression in the small intestine (P < 0.05). Furthermore, E153 or E171 exposed rats had shorter telomeres in the lung (P < 0.05). Plasma from particle-exposed rats also produced telomere shortening in cultured lung epithelial cells. There were unaltered levels of oxidatively damaged DNA in the liver and lung and no changes in the DNA repair activity of oxidatively damaged DNA in the lung. Altogether, these results indicate that intragastric exposure to E153 and E171 is associated with reduced tight junction protein expression in the intestinal barrier and telomere length shortening in the lung in rats.
Identifiants
pubmed: 30852617
pii: 5372975
doi: 10.1093/mutage/gez003
doi:
Substances chimiques
Food Additives
0
Occludin
0
Ocln protein, rat
0
Reactive Oxygen Species
0
titanium dioxide
15FIX9V2JP
Carbon
7440-44-0
Titanium
D1JT611TNE
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
203-214Informations de copyright
© The Author(s) 2019. Published by Oxford University Press on behalf of the UK Environmental Mutagen Society. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.