Syringin alleviates bisphenol A-induced spermatogenic defects and testicular injury by suppressing oxidative stress and inflammation in male zebrafish

•SRG shields zebrafish testes from BPA-induced damage, preserving sperm quality and reproductive function.•This study uncovers SRG's molecular mechanisms for protecting against oxidative stress and inflammation.•SRG holds promise as a therapeutic candidate for mitigating spermatogenic defects a...

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Veröffentlicht in:International immunopharmacology 2024-04, Vol.131, p.111830-111830, Article 111830
Hauptverfasser: Zhao, Ye, Luo, Xu, Hu, Jinyuan, Panga, Mogellah John, Appiah, Clara, Du, Zhanxiang, Zhu, Lin, Retyunskiy, Vladimir, Gao, Xing, Ma, Bo, Zhang, Qi
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Sprache:eng
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Zusammenfassung:•SRG shields zebrafish testes from BPA-induced damage, preserving sperm quality and reproductive function.•This study uncovers SRG's molecular mechanisms for protecting against oxidative stress and inflammation.•SRG holds promise as a therapeutic candidate for mitigating spermatogenic defects and testicular injury, benefiting male reproductive health. Syringin (SRG) is a bioactive principle possessing extensive activities including scavenging of free radicals, inhibition of apoptosis, and anti-inflammatory properties. However, its effects on spermatogenic defects and testicular injury as well as the underlying mechanisms are still unclear. This study aims to investigate the protective effect of SRG on testis damage in zebrafish and explore its potential molecular events. Zebrafish testicular injury was induced by exposure to bisphenol A (BPA) (3000 μg/L) for two weeks. Fish were treated with intraperitoneal injection of SRG at different doses (5 and 50 mg/kg bodyweight) for two more weeks under BPA induction. Subsequently, the testis and sperm were collected for morphological, histological, biochemical and gene expression examination. It was found that the administration of SRG resulted in a significant protection from BPA-caused impact on sperm concentration, morphology, motility, fertility rate, testosterone level, spermatogenic dysfunction and resulted in increased apoptotic and reactive oxygen species’ levels. Furthermore, testicular transcriptional profiling alterations revealed that the regulation of inflammatory response and oxidative stress were generally enriched in differentially expressed genes (DEGs) after SRG treatment. Additionally, it was identified that SRG prevented BPA-induced zebrafish testis injury through upregulation of fn1a, krt17, fabp10a, serpina1l and ctss2. These results indicate that SRG alleviated spermatogenic defects and testicular injury by suppressing oxidative stress and inflammation in male zebrafish.
ISSN:1567-5769
1878-1705
DOI:10.1016/j.intimp.2024.111830