Effects of subchronic samarium exposure on the histopathological structure and apoptosis regulation in mouse testis

Environ Toxicol Pharmacol. 2014 Mar;37(2):505-12. doi: 10.1016/j.etap.2014.01.007. Epub 2014 Jan 21.

Abstract

To evaluate the reproductive toxicity of samarium, a widely used rare earth element, male ICR mice were orally exposed to samarium nitrate for 90 days for lesion evaluation in the testis. Decreased organ coefficients, disorganized seminiferous tubules, and decreased spermatogenic cells and sperm of the testis were observed extensively in the treated groups, indicating that the testis is a target organ of samarium. Electron microscopy confirmed that the lesions inside the spermatogenic cells and sperm mainly included mitochondrial swelling, mitochondrial vacuolization, fuzzy nuclear membranes, and marginated chromatin. Increased spermatogenic cell apoptosis rate in the testis was confirmed with a TUNEL assay. And expression up-regulation of p53 and Bax, and down-regulation of Bcl-2 were observed (p<0.05), indicating the apoptosis is related to p53 mediated pathway.

Keywords: Apoptosis; Bcl-2; Mouse testis; Samarium nitrate; Ultra-structure.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Luteinizing Hormone / blood
  • Male
  • Mice, Inbred ICR
  • Proto-Oncogene Proteins c-bcl-2 / genetics
  • Samarium / toxicity*
  • Testis / drug effects*
  • Testis / metabolism
  • Testis / pathology
  • Testosterone / blood
  • bcl-2-Associated X Protein / genetics

Substances

  • Bax protein, mouse
  • Proto-Oncogene Proteins c-bcl-2
  • bcl-2-Associated X Protein
  • Testosterone
  • Samarium
  • Luteinizing Hormone