PFOA evokes extracellular Ca influx and compromises progesterone-induced response in human sperm.

Chemosphere

Department of Physiology, School of Basic Medical Sciences, Jiangxi Provincial Key Laboratory of Reproductive Physiology and Pathology, Nanchang University, Nanchang, 330006, PR China. Electronic address:

Published: February 2020

Perfluorooctane acid (PFOA), a persistent organic pollutant, is ubiquitously present in the environment and may detrimentally affect male reproductive health. In this study, mature human sperm were in vitro exposed to different concentrations of PFOA (0.25, 2.5 or 25 μg/ml) alone or in combination with progesterone (P4) to evaluate the toxicity and the potential mechanism of action. Exposure to high-dose PFOA (25 μg/ml) alone for 4 h caused a decline in capacity of human spermatozoa to penetrate synthetic mucus, with an increased production of reactive oxygen species (ROS). Furthermore, PFOA treatment (2.5 and 25 μg/ml) evoked a transient rise in intracellular calcium concentration [Ca] by activating the sperm-specific CatSper channel. However, preincubation with PFOA (2.5-25 μg/ml) for 4 h significantly suppressed P4-stimulated extracellular Ca influx in human spermatozoa. Moreover, PFOA pretreatment at all concentrations evaluated markedly compromised P4-induced acrosome reaction and sperm penetration into viscous medium. Taken together, these results suggest that PFOA exposure may impair human sperm function through inducing oxidative stress and disturbing P4-induced Ca signaling.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.chemosphere.2019.125074DOI Listing

Publication Analysis

Top Keywords

human sperm
12
pfoa
8
extracellular influx
8
human spermatozoa
8
human
5
pfoa evokes
4
evokes extracellular
4
influx compromises
4
compromises progesterone-induced
4
progesterone-induced response
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!