AI Article Synopsis

  • The study evaluated the toxic effects of paracetamol and oxytetracycline on the marine rotifer Brachionus rotundiformis, finding that even low concentrations can induce oxidative stress and increase detoxification enzyme activity.
  • Despite the oxidative stress, the rotifers showed no significant changes in population growth, indicating they can tolerate these pharmaceuticals better than previously thought.
  • Gene expression analysis revealed specific cytochrome P450 and glutathione S-transferase genes are involved in detoxifying these drugs, supporting the idea that low-level exposure does not adversely affect rotifer populations.

Article Abstract

To investigate the adverse effect of two widely used pharmaceuticals, paracetamol (acetaminophen [APAP]) and oxytetracycline (OTC) on the marine rotifer Brachionus rotundiformis (B. rotundiformis), the animals were exposed to various environmentally-relevant concentrations. Up to date, acetaminophen and oxytetracycline have been considered as toxic, if used above threshold concentration, i.e. overdosed. However, this study demonstrated these two pharmaceuticals even at low concentration (i.e., μg/L scale) elicited oxidative stress through the generation of reactive oxygen species (ROS) along with the increased glutathione S-transferase activity, despite no-observed effect in in-vivo population growth. To validate the adverse effects of the two pharmaceuticals at relatively low concentrations, mRNA expression analysis was performed of the entire set of genes encoding 26 cytochrome P450s (CYPs) of phase I and 19 glutathione S-transferases (GSTs) of phase II of the rotifer B. rotundiformis. The mRNA expression analysis suggested specific genes CYP3045A2 and GSTσ1, GSTσ4, and GSTω1 take part in detoxification of APAP and OTC, resulting in no significant changes in the population growth and undetermined no observed effect concentration (NOEC) in the marine rotifer B. rotundiformis.

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Source
http://dx.doi.org/10.1016/j.aquatox.2018.08.018DOI Listing

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