AI Article Synopsis

  • The study investigated the antagonistic effects of acrylamide (AA) and ethanol (Et) on the bone quality of adult mice divided into four groups: one receiving AA, one receiving Et, one receiving both, and a control group.
  • Individual and combined exposure to AA and Et did not significantly affect body weight or bone length/weight, but notable changes in liver enzymes and bone health markers were observed.
  • The results indicated that both toxins negatively impacted bone health parameters, with the greatest effects seen in the group that received both substances simultaneously.

Article Abstract

The aim of present study was to verify antagonistic effect of acrylamide (AA) and ethanol (Et) on bone quality parameters. Adult mice ( = 20) were segregated into four groups following 2 weeks administration of toxins: group E1, which received AA (20 mg/kg body weight daily); group E2, which received 15% Et (1.7 g 100% Et/kg body weight daily); group E12, which received simultaneously both toxins; and a control group. An insignificant impact of individual applications of AA, Et or their simultaneous supplementation on the total body weight of mice and the length and weight of their femoral bones was identified. In group E1, higher levels of alanine aminotransferase (ALT), aspartate aminotransferase (AST), triglyceride (TG), a decreased level of glutathione (GSH) and elevated endocortical bone remodelling were determined. A significantly lower relative volume of cortical bone, bone mineral density (BMD), elevated endocortical bone remodelling and cortical porosity, higher levels of ALT, AST, lower values for total proteins (TP), GSH, alkaline phosphatase (ALP), calcium, and phosphorus were recorded in group E2. In the mice from group E12, the highest endocortical bone remodelling, decreased values for BMD, TP, GSH and ALP and increased levels of ALT and AST were found. Our findings confirmed the antagonistic impact of AA and Et at doses used in this study on biochemical and morphological parameters consistent with bone health in an animal model.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7600557PMC
http://dx.doi.org/10.3390/ani10101835DOI Listing

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