Liao Tian-Long, He Cai-Mei, Xiao Di, Zhang Zhi-Rong, He Zuping, Yang Xiao-Ping
Key Laboratory of Study and Discovery of Small Targeted Molecules of Hunan Province, The Key Laboratory of Model Animals and Stem cell Biology in Hunan Province, The Engineering Research Center of Reproduction and Translational Medicine of Hunan Province, Hunan Normal University School of Medicine, Changsha 410013, China.
Department of Cardiology, Zhuzhou Hospital, The Affiliated Hospital of Xiangya Medical College of Central South University, Zhuzhou 412001, China.
Asian J Androl. 2025 Jul 1;27(4):543-549. doi: 10.4103/aja2024106. Epub 2025 Jan 7.
Icariin is a pure compound derived from Epimedium brevicornu Maxim, and it helps the regulation of male reproduction. Nevertheless, the role and underlying mechanisms of Icariin in mediating male germ cell development remain to be clarified. Here, we have demonstrated that Icariin promoted proliferation and DNA synthesis of mouse spermatogonial stem cells (SSCs). Furthermore, surface plasmon resonance iron (SPRi) and molecular docking (MOE) assays revealed that phosphodiesterase 5A (PDE5A) was an important target of Icariin in mouse SSCs. Mechanically, Icariin decreased the expression level of PDE5A. Interestingly, hydrogen peroxides (H 2 O 2 ) enhanced the expression level of phosphorylation H2A.X (p-H2A.X), whereas Icariin diminished the expression level of p-H2A.X and DNA damage caused by H 2 O 2 in mouse SSCs. Finally, our in vivo animal study indicated that Icariin protected male reproduction. Collectively, these results implicate that Icariin targets PDE5A to regulate mouse SSC viability and DNA damage and improves male reproductive capacity. This study thus sheds new insights into molecular mechanisms underlying the fate decisions of mammalian SSCs and offers a scientific basis for the clinical application of Icariin in male reproduction.
淫羊藿苷是一种从短角淫羊藿中提取的纯化合物,它有助于调节雄性生殖。然而,淫羊藿苷在介导雄性生殖细胞发育中的作用及潜在机制仍有待阐明。在此,我们证明了淫羊藿苷可促进小鼠精原干细胞(SSCs)的增殖和DNA合成。此外,表面等离子体共振铁(SPRi)和分子对接(MOE)分析表明,磷酸二酯酶5A(PDE5A)是淫羊藿苷在小鼠SSCs中的重要靶点。机制上,淫羊藿苷降低了PDE5A的表达水平。有趣的是,过氧化氢(H2O2)可提高磷酸化H2A.X(p-H2A.X)的表达水平,而淫羊藿苷可降低小鼠SSCs中p-H2A.X的表达水平以及由H2O2引起的DNA损伤。最后,我们的体内动物研究表明淫羊藿苷可保护雄性生殖。总的来说,这些结果表明淫羊藿苷靶向PDE5A来调节小鼠SSC的活力和DNA损伤,并提高雄性生殖能力。因此,本研究为哺乳动物SSCs命运决定的分子机制提供了新的见解,并为淫羊藿苷在雄性生殖中的临床应用提供了科学依据。