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Toxic effects of mineral oil saturated hydrocarbons (MOSH) and relation to accumulation in rat liver.

Unni Cecilie NygaardÅshild VegeTorleiv RognumKoni GrobChristel CartierJean-Pierre CravediJan Alexander
Published in: Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association (2023)
Humans are daily exposed to mineral oil saturated hydrocarbons (MOSH) from the diet. We exposed female Fischer 344 rats to a broad mixture and sub-fractions of MOSH. Chemical characterization of the MOSH mixture used and material accumulated in rat tissues were previously reported (Barp et al. 2017a, 2017b). Rats were exposed to feed containing 0-4000 mg/kg broad MOSH mixture for 30, 60, 90 and 120 days; and for 120 days to feed containing different MOSH fractions: i) mainly molecular masses < C25 (S-C25), ii) dewaxed, mainly molecular masses > C25 (L-C25) and iii) the L-C25 fraction mixed with wax largely consisting of n-alkanes > C25 (L-C25W). Treatments related effects were increased liver and spleen weight, as well as vacuolization and granuloma formation with lymphoid cell clusters in the liver, but effects varied strongly between the MOSH fractions tested. We conclude that increased liver and spleen weights were related to accumulated n-alkanes (wax) above C25, presumably not relevant for humans, but also to MOSH from S-C25, mainly consisting of iso-alkanes and substituted cycloalkanes below C25 with a small proportion of n-alkanes. Induction of liver granuloma appeared to be related to n-alkanes > C25 and not to the accumulated amount of MOSH. Immune responses to an injected antigen were not affected. Iso-alkanes and substituted cycloalkanes accumulating in rat liver and spleen were similar to those accumulating in humans.
Keyphrases
  • immune response
  • physical activity
  • oxidative stress
  • contrast enhanced
  • stem cells
  • gene expression
  • magnetic resonance
  • bone marrow
  • dendritic cells
  • molecular docking
  • inflammatory response
  • fine needle aspiration