Effects of fluoxetine on behavior, antioxidant enzyme systems, and multixenobiotic resistance in the Asian clam Corbicula fluminea

Chemosphere. 2015 Jan:119:856-862. doi: 10.1016/j.chemosphere.2014.08.062. Epub 2014 Sep 19.

Abstract

Fluoxetine (FLX), a selective serotonin reuptake inhibitor, is widespread in aquatic environments. Despite its reported effects on behavior and reproduction in aquatic species, little is known about the effects of FLX on cellular detoxification and defense system in bivalves. Here, the adult Asian clam (Corbicula fluminea) was exposed to 0.5, 5, and 50 μg L(-1) FLX for 30 d. Siphoning behavior was inhibited by treatment with 50 μg L(-1) FLX. Additionally, superoxide dismutase (SOD) activity in the gills and digestive glands significantly decreased (p<0.05) with 5 and 50 μg L(-1) FLX treatments, whereas catalase (CAT) activity and malondialdehyde (MDA) content markedly increased (p<0.05). Moreover, transcription of thioredoxin reductase (TR), glutathione peroxidase (GPx) and Glutathione S-transferase pi class (GSTpi) was significantly upregulated (p<0.05), whereas glutathione reductase (GR) was markedly downregulated (p<0.05). These findings suggest that FLX affects behavior and induces oxidative stress in C. fluminea. The downregulation of ATP-binding cassette (ABC) transportor genes (ABCB1, ABCC1 and ABCG2) transporter genes indicated that FLX might suppress the multixenobiotic resistance (MXR) system in C. fluminea. Our results provide new insights into the adverse effects of FLX on the cellular detoxification and MXR system of C. fluminea.

Keywords: Antioxidant enzymes; C. fluminea; Fluoxetine; Multixenobiotic resistance; Siphoning behavior.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analysis of Variance
  • Animals
  • Antioxidants / metabolism
  • Behavior, Animal / drug effects*
  • Catalase / metabolism
  • China
  • Corbicula / drug effects*
  • Corbicula / genetics
  • DNA Primers / genetics
  • DNA, Complementary / genetics
  • Dose-Response Relationship, Drug
  • Fluoxetine / metabolism
  • Fluoxetine / toxicity*
  • Gills / metabolism
  • Glutathione Peroxidase / metabolism
  • Glutathione Reductase / metabolism
  • Malondialdehyde / metabolism
  • Oxidative Stress / drug effects
  • Real-Time Polymerase Chain Reaction
  • Superoxide Dismutase / metabolism
  • Thioredoxin-Disulfide Reductase / metabolism
  • Water Pollutants, Chemical / analysis
  • Water Pollutants, Chemical / toxicity*

Substances

  • Antioxidants
  • DNA Primers
  • DNA, Complementary
  • Water Pollutants, Chemical
  • Fluoxetine
  • Malondialdehyde
  • Catalase
  • Glutathione Peroxidase
  • Superoxide Dismutase
  • Glutathione Reductase
  • Thioredoxin-Disulfide Reductase