Co-exposure to polystyrene nanoplastics and hexachlorocyclohexane induces enhanced human sperm toxicity in vitro

  • Reprod Toxicol. 2026 Apr:141:109201. doi: 10.1016/j.reprotox.2026.109201.
Pengbin Liu  1 Dan Wang  2 Yan Zeng  3 Hailang Wang  1 Fenglong Wan  1 Jiancheng Wu  1 Yong Huang  1 Lichen Zeng  1 Liyan Yan  4
Affiliations
  • 1. Affiliated Hospital of Jinggangshan University, Ji'an, Jiangxi, China.
  • 2. Ji'an Central People's Hospital, Ji'an, Jiangxi, China.
  • 3. Ji'an Kangming Eye Hospital, Ji'an, Jiangxi, China.
  • 4. Ji'an Central People's Hospital, Ji'an, Jiangxi, China. Electronic address: [email protected].
Abstract

The decline in global male fertility has been increasingly linked to exposure to environmental contaminants. This study investigates the combined toxicity of polystyrene nanoplastics (PS-NPs) and hexachlorocyclohexane (HCH, a type of persistent organic pollutants (POPs)) on human sperm function in vitro. Sperm samples from healthy donors were exposed to PS-NPs, HCH, or both, and key functional parameters, including motility, penetration ability, capacitation, acrosome reaction, Reactive Oxygen Species (ROS) content, and mitochondrial membrane potential (MMP) were assessed. Results demonstrated that co-exposure to PS-NPs and HCH could enhance toxicity to cause a marked decline in sperm viability, motility, and penetration capacity compared to individual exposures. Moreover, co-treatment markedly elevated intracellular ROS ([ROS]i), reduced MMP, and inhibited progesterone-induced capacitation and acrosome reaction. Network pharmacology and the followed western blot (WB) analysis demonstrated an upregulation of pro-apoptotic proteins (Caspase-3 and Bax) and downregulation of Bcl-2, indicating activation of mitochondrial apoptotic pathways. These findings provide the first evidence that co-exposure to PS-NPs and HCH could induce enhanced spermatotoxicity, likely attributable to oxidative stress and mitochondrial dysfunction, highlighting a potential environmental risk factor in idiopathic male infertility.

Keywords
Co-exposure; Human sperm; Mitochondrial dysfunction; Network pharmacology; Oxidative stress.
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