Nirmatrelvir has detrimental effects on sperm function by altering the PI3K/PDK1/AKT signaling pathway

Eun Ju Jung, Jae Hwan Jo, Claudine Uwamahoro, Seung Ik Jang, Ju Mi Hwang, Woo Jin Lee, Jeong Won Bae, Do Yeal Ryu, Woo Sung Kwon

Research output: Contribution to journalArticlepeer-review

Abstract

Nirmatrelvir (NMV) is a recently developed selective inhibitor of the main protease of Sars-Cov-2 that reduces the severity of infection. Despite its widespread use and various side effects, NMV's effect on male fertility is still unclear. This study was thus established to investigate how NMV affects male fertility. For experiments, Duroc spermatozoa were incubated with various concentrations of NMV (0, 0.1, 1, 10, 50, and 100 μM). Then, sperm motility, motion kinematics, capacitation status, intracellular ATP level, and cell viability were evaluated. In addition, the expression levels of phospho-PKA substrates, tyrosine-phosphorylated proteins, and PI3K/PDK1/AKT signaling pathway-related proteins were measured by western blotting. Our results showed that sperm motility, motion kinematics, proportion of capacitated spermatozoa, and intracellular ATP level were significantly decreased by NMV in a dose-dependent manner. Moreover, PKA activation was significantly suppressed by NMV, and expression levels of PI3K, phospho-PDK1, AKT, and phospho-AKT (Thr308 and Ser473) were significantly increased in a dose-dependent manner. Combining these findings, it is suggested that NMV has detrimental effects on sperm function by inducing abnormal changes in the PI3K/PDK1/AKT signaling pathway, resulting in PKA deactivation. Therefore, there is a need to pay particular attention to its male reproductive toxicity when NMV is administered.

Original languageEnglish
Article number105848
JournalToxicology in Vitro
Volume99
DOIs
StatePublished - Aug 2024

Keywords

  • Capacitation
  • Nirmatrelvir
  • PI3K/PDK1/AKT signaling pathway
  • Sperm function

Fingerprint

Dive into the research topics of 'Nirmatrelvir has detrimental effects on sperm function by altering the PI3K/PDK1/AKT signaling pathway'. Together they form a unique fingerprint.

Cite this