Green tea extract as a cryoprotectant additive to preserve the motility and DNA integrity of human spermatozoa

• Published in: Asian journal of andrology 2021-03, Vol.23 (2), p.150-156
• Main Authors: Alqawasmeh, Odai, Zhao, Mingpeng, Chan, Carol, Leung, Maran, Chow, Ki, Agarwal, Nikunj, Mak, Jennifer, Wang, Chi, Pang, Chi, Li, Tin, Chu, Wai, Chan, David
• Format: Article
• Language: English
• Subjects: Antioxidants; antioxidants; cryopreservation additives; sperm cryopreservation; sperm dna fragmentation; sperm motility; Cryopreservation; Cryoprotective Agents - pharmacology; DNA; DNA - drug effects; Green tea; Humans; Hydrogen Peroxide - pharmacology; Male; Motility; Original; Oxidants - pharmacology; Oxidative stress; Oxidative Stress - drug effects; Plant Extracts - pharmacology; Reactive oxygen species; Reactive Oxygen Species - metabolism; Semen Preservation; Sperm; Sperm Motility - drug effects; Spermatozoa; Spermatozoa - drug effects; Spermatozoa - metabolism; Tea
• ISSN: 1008-682X; 1745-7262
• DOI: 10.4103/aja.aja_58_20

Cryopreservation impairs sperm quality and functions, including motility and DNA integrity. Antioxidant additives in sperm freezing media have previously brought improvements in postthawed sperm quality. Green tea extract (GTE) is widely considered as an excellent antioxidant, and its beneficial role has been proven in other human cells. This study aims to evaluate the GTE as a potential additive in cryopreservation media of human spermatozoa. In part one, the semen of 20 normozoospermic men was used to optimize the concentration of GTE that maintains sperm motility and DNA integrity against oxidative stress, induced by hydrogen peroxide (H2O2). Spermatozoa were treated with GTE at different concentrations before incubation with H2O2. In part two, the semen of 45 patients was cryopreserved with or without 1.0 ng ml−1 GTE. After 2 weeks, the semen was thawed, and the effect on sperm motility and DNA fragmentation was observed. Our data showed that GTE significantly protected sperm motility and DNA integrity against oxidative stress induced by H2O2when added at a final concentration of 1.0 ng ml−1. We found that the addition of 1.0 ng ml−1 GTE to cryopreservation media significantly increased sperm motility and DNA integrity (both P < 0.05). More interestingly, patients with high sperm DNA damage benefited similarly from the GTE supplementation. However, there was no significant change in the reactive oxygen species (ROS) level. In conclusion, supplementing sperm freezing media with GTE has a significant protective effect on human sperm motility and DNA integrity, which may be of clinical interest.