Decreased expression of AKAP4 and TyrPho proteins in testis, epididymis, and spermatozoa with low sexual performance of mice induced by modified CUMS

Andrologia. 2021 Apr;53(3):e13977. doi: 10.1111/and.13977. Epub 2021 Jan 24.

Abstract

The molecular mechanism of chronic stress especially reduced motility, a major cause of male infertility, has not been proved. It is known that A-kinase anchor protein 4 (AKAP4) and tyrosine-phosphorylated (TyrPho) proteins are involved in progressive motility. This study aimed to investigate the effect of chronic unpredictable mild stress (CUMS) on sexual behaviours, sperm quality, and expressions of AKAP4 and TyrPho proteins in testis, epididymis, and spermatozoa. Sixteen male mice were divided into control and CUMS groups (n = 8/group). Animals were induced by a stressor from twelve stressors for 36 days. Sexual behaviours, corticosterone and testosterone, sperm parameters, and histopathology were observed. The expressions of AKAP4 and TyrPho proteins in testis, epididymis, and spermatozoa were examined. Results showed that CUMS significantly increased corticosterone while serum testosterone level was decreased. Sexual behaviours and sperm parameter quality were significantly decreased. CUMS mice showed vacuolisation and pyknotic cells in seminiferous epithelium and less sperm mass was observed within epididymal lumen. CUMS decreased expressions of AKAP4 and TyrPho proteins in testis, epididymis, and spermatozoa. In conclusion, the decreased expression of AKAP4 and TyrPho proteins may be a mechanism associated with low semen qualities particularly decrease of sperm motility in CUMS.

Keywords: A-kinase anchor protein 4; chronic unpredictable mild stress; epididymis; spermatozoa; tyrosine-phosphorylated proteins.

MeSH terms

  • A Kinase Anchor Proteins / genetics*
  • A Kinase Anchor Proteins / metabolism
  • Animals
  • Epididymis* / metabolism
  • Humans
  • Male
  • Mice
  • Phosphorylation
  • Sperm Motility
  • Spermatozoa / metabolism
  • Testis* / metabolism
  • Tyrosine

Substances

  • A Kinase Anchor Proteins
  • Akap4 protein, mouse
  • Tyrosine