Na Li1, Hang Kang2, Zhen Peng3, Hua-Feng Wang2, Shi-Qi Weng2, Xu-Hui Zeng4. 1. Clinical Medical Research Center, Yichun People's Hospital, Yichun, Jiangxi 336000, PR China; Institute of Life Science, Nanchang University, Nanchang, Jiangxi 330031, PR China; Laboratory Department, Affiliated Reproductive Hospital of Jiangxi University of Traditional Chinese Medicine, Nanchang, Jiangxi 330031, PR China. 2. Institute of Life Science, Nanchang University, Nanchang, Jiangxi 330031, PR China. 3. Clinical Medical Research Center, Yichun People's Hospital, Yichun, Jiangxi 336000, PR China; Institute of Life Science, Nanchang University, Nanchang, Jiangxi 330031, PR China. 4. Institute of Reproductive Medicine, School of Medicine, Nantong University, Nantong, Jiangsu 226000, PR China; Institute of Life Science, Nanchang University, Nanchang, Jiangxi 330031, PR China. Electronic address: zengxuhui@ntu.edu.cn.
Abstract
BACKGROUND: Bisphenol A (BPA), a widely used plastic monomer and plasticizer, is detectable in blood, urine and semen of a healthy people, with concentrations ranging from 0.1 nM to 10 nM. It has been shown that in vitro exposure of BPA as low as 0.001 nM could significantly inhibited mouse sperm motility and acrosome reaction. However, it is still unclear whether BPA at those physiologically detectable concentration affects human sperm. METHODS: The effects of different concentrations of BPA (0, 10-3, 10-2, 10-1, 10, 103 nM) on sperm functions were examined, including human sperm viability, kinematic parameters, hyperactivation and capacitation. RESULTS: BPA caused a remarkable decline in human sperm viability, motility and progressive motility, hyperactivation, capacitation and progesterone-induced acrosome reaction. Mechanism studies showed that BPA could suppress the protein tyrosine phosphorylation level of human sperm, but had no effect on sperm calcium signaling. CONCLUSIONS: Physiologically detectable concentrations of BPA may impair human sperm functions via suppressing protein tyrosine phosphorylation of human sperm, implying that environmental pollution of BPA might be a factor contributing to male infertility.
BACKGROUND:Bisphenol A (BPA), a widely used plastic monomer and plasticizer, is detectable in blood, urine and semen of a healthy people, with concentrations ranging from 0.1 nM to 10 nM. It has been shown that in vitro exposure of BPA as low as 0.001 nM could significantly inhibited mouse sperm motility and acrosome reaction. However, it is still unclear whether BPA at those physiologically detectable concentration affects human sperm. METHODS: The effects of different concentrations of BPA (0, 10-3, 10-2, 10-1, 10, 103 nM) on sperm functions were examined, including human sperm viability, kinematic parameters, hyperactivation and capacitation. RESULTS:BPA caused a remarkable decline in human sperm viability, motility and progressive motility, hyperactivation, capacitation and progesterone-induced acrosome reaction. Mechanism studies showed that BPA could suppress the protein tyrosine phosphorylation level of human sperm, but had no effect on sperm calcium signaling. CONCLUSIONS: Physiologically detectable concentrations of BPA may impair human sperm functions via suppressing protein tyrosine phosphorylation of human sperm, implying that environmental pollution of BPA might be a factor contributing to male infertility.