Repeated administrations of Mn3O4 nanoparticles cause testis damage and fertility decrease through PPAR-signaling pathway

Nanotoxicology. 2020 Apr;14(3):326-340. doi: 10.1080/17435390.2019.1695976. Epub 2020 Jan 7.

Abstract

Potential health hazards of nanomaterials on male reproductive system have received raising concerns. Even though Mn3O4 nanoparticles (Mn3O4-NPs) is highly effective in clinical diagnostic and therapeutic applications of human disease, its potential toxic effect on the male reproductive system has not been reported. In this study, the testis damage and fertility decrease of male rats were conducted to testify the experimental reproductive injury induced by Mn3O4-NPs. After repeated tail vein injection with 10 mg/kg/week Mn3O4-NPs for 0, 60 and 120 days, Mn3O4-NPs accumulated in the testes resulted in oxidative stress and disorder of normal serum sex hormones. Experiments in vivo and in vitro indicated that mitochondria-mediated cell apoptosis were triggered via oxidative stress, demonstrated by the upregulation of malondialdehyde (MDA) and the depolarization of mitochondrial membrane potential. Notably, Mn3O4-NPs significantly resulted in a reduction of the quantity/quality of sperm and finally caused astonishing fertility decrease. Our preliminary result implied that the application of Mn3O4-NPs could be a double-edged sword and careful consideration should be given to the clinical uses.

Keywords: Mn3O4 nanoparticles; apoptosis; fertility decrease; testis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Fertility / drug effects*
  • Humans
  • Male
  • Manganese Compounds / chemistry
  • Membrane Potential, Mitochondrial / drug effects
  • Nanoparticles / chemistry
  • Nanoparticles / toxicity*
  • Oxidative Stress / drug effects
  • Oxides / chemistry
  • Oxides / toxicity*
  • Peroxisome Proliferator-Activated Receptors / metabolism*
  • Rats
  • Rats, Sprague-Dawley
  • Signal Transduction
  • Testis / drug effects*
  • Testis / metabolism
  • Testis / pathology

Substances

  • Manganese Compounds
  • Oxides
  • Peroxisome Proliferator-Activated Receptors
  • manganese oxide