Apoptosis and p53 gene expression in male reproductive tissues of cadmium exposed rats

Biometals. 1999 Jun;12(2):131-9. doi: 10.1023/a:1009273711068.

Abstract

Reverse transcription (RT) PCR technique was used to investigate the mechanism of apoptosis induced by Cd and the change of its related genes in testes and prostate of rats. Adult male rats were given a single (s.c.) injection of CdCl2 0, 2.5, 5.0, 10 mumol/kg. 48 h and 72 h after administration of Cd, animals were sacrificed. The results indicated that Cd can induce apoptosis in testes via p53-independent pathway. No apoptosis occurred in prostate in any of the Cd-exposed groups. There was a clearly negative relationship in testes between p53 gene expression and Cd exposure and this dose-response relationship was observed both at 48 h and 72 h. There was a very small increase of this gene expression in the dorsolateral lobe of the prostate in Cd exposed groups. The other apoptosis related gene, bcl-x, was not detectable in either control or Cd-exposed group in testes and dorsal prostate. Although the MT-I gene was expressed in testes or dorsal prostate both in control and exposed groups, no overexpression of MT-I gene was found after administration of Cd. The expression of MT-I in the ventral prostate was not detected in the control group, but a weak expression was found after Cd exposure. Since p53 is a tumor suppressor gene which can inhibit tumorigenesis, the consequence of a Cd-induced decrease of p53 in testes may have a relation to the known risk of Cd tumorigenesis in this tissue.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects*
  • Cadmium / toxicity*
  • Gene Expression / drug effects
  • Genes, p53*
  • Male
  • Metallothionein / genetics
  • Prostate / drug effects*
  • Prostate / metabolism
  • Prostate / pathology
  • RNA, Messenger / analysis
  • Rats
  • Rats, Wistar
  • Reproducibility of Results
  • Testis / drug effects*
  • Testis / metabolism
  • Testis / pathology

Substances

  • RNA, Messenger
  • Cadmium
  • Metallothionein