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Phosphopeptide Analysis of Rodent Epididymal Spermatozoa
Published on: December 30, 2014
Abamectin disrupts sperm function through the alteration of PKA activity and tyrosine phosphorylation in boar
Claudine Uwamahoro1, Jae-Hwan Jo1, Seung-Ik Jang1
1Department of Animal Science and Biotechnology, Kyungpook National University, Sangju 37224, Republic of Korea.
Abstract:
The potential toxicity of abamectin (ABM), a macrocyclic lactone insecticide widely used in agriculture, in non-target organisms has raised concerns. Therefore, this study aimed to investigate the effects of ABM on sperm function, focusing on motility, kinematics, ATP levels, viability, protein kinase A (PKA) activity, and tyrosine phosphorylation. Boar spermatozoa were incubated with various ABM concentrations (0, 1, 5, 10, 15, 25, 50, and 100 µM) under capacitating conditions and assessed through computer-assisted sperm analysis, Hoechst 33258/chlortetracycline staining, ATP and viability assays, and Western blotting. The results revealed a dose-dependent decline in sperm motility and ATP levels starting at 10 µM. Sperm capacitation was significantly altered at concentrations of at least 25 µM, with an increase in capacitated spermatozoa and a decrease in non-capacitated spermatozoa. However, overall cell viability remained unaffected. Western blot analysis showed abnormal alterations in PKA substrates and tyrosine-phosphorylated proteins. These findings suggest ABM disrupts sperm function and key fertilization pathways, indicating potential risks to male fertility.

