Cadmium exposure caused cardiotoxicity in common carps (Cyprinus carpio L.): miR-9-5p, oxidative stress, energetic impairment, mitochondrial division/fusion imbalance, inflammation, and autophagy

Fish Shellfish Immunol. 2023 Jul:138:108853. doi: 10.1016/j.fsi.2023.108853. Epub 2023 May 27.

Abstract

Cadmium (Cd), a toxic heavy metal pollutant, is a threat to human and eatable fish health. Common carps are widely cultivated and eaten by humans. However, there are no reports about Cd-damaged common carp hearts. Our experiment attempted to investigate the cardiotoxicity of Cd to common carps by establishing a common carp Cd exposure model. Our results showed that Cd injured hearts. Moreover, Cd treatment induced autophagy via miR-9-5p/Sirt1/mTOR/ULK1 pathway. Cd exposure caused oxidant/antioxidant imbalance and oxidative stress; and led to energetic impairment. Energetic impairment partook in oxidative stress-mediated autophagy through AMPK/mTOR/ULK1 pathway. Furthermore, Cd caused mitochondrial division/fusion imbalance and resulted in inflammatory injury via NF-κB-COX-2-PTGEs and NF-κB-COX-2-TNF-α pathways. Oxidative stress mediated mitochondrial division/fusion imbalance, further induced inflammation and autophagy via OPA1/NF-κB-COX-2-TNF-α-Beclin1 and OPA1/NF-κB-COX-2-TNF-α/P62 pathways under Cd treatment. Taken together, miR-9-5p, oxidative stress, energetic impairment, mitochondrial division/fusion imbalance, inflammation, and autophagy participated in the mechanism of Cd-cardiotoxicity to common carps. Our study revealed harmful effect of Cd on hearts, and provided new information for researches of environmental pollutant toxicity.

Keywords: Autophagic injury; Energetic impairment; Heavy metal; Mitochondrial dynamics; NF-κB-COX-2 axis; microRNA-9-5p.

MeSH terms

  • Animals
  • Autophagy
  • Cadmium / toxicity
  • Cardiotoxicity
  • Carps* / metabolism
  • Cyclooxygenase 2
  • Humans
  • Inflammation / chemically induced
  • Inflammation / veterinary
  • MicroRNAs* / metabolism
  • NF-kappa B / metabolism
  • Oxidative Stress
  • TOR Serine-Threonine Kinases / metabolism
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Cadmium
  • NF-kappa B
  • Tumor Necrosis Factor-alpha
  • Cyclooxygenase 2
  • MicroRNAs
  • TOR Serine-Threonine Kinases