Reproductive Medicine Research Group, School of Medicine, Ninewells Hospital and Medical School, University of Dundee, Dundee, UK.
Emerging Innovations Unit, Discovery Sciences, R&D, AstraZeneca, Cambridge, UK.
Hum Reprod. 2021 Feb 18;36(3):560-570. doi: 10.1093/humrep/deaa328.
Does AZD5904, a myeloperoxidase inhibitor (MPOi), have any effect on human sperm function in vitro?
AZD5904 improves sperm function in an in vitro model of oxidative stress (OS) and potentially offers a novel treatment approach for male infertility.
Male infertility is an underlying or contributory cause in half of all couples experiencing difficulties conceiving, yet there is currently no effective treatment or cure. OS is a common pathology in a significant proportion of infertile men. It can negatively affect sperm motility and the ability to fertilize a mature oocyte, as well as DNA integrity, and therefore represents an attractive target for therapeutic intervention.
STUDY DESIGN, SIZE, DURATION: This study included population-based samples from men (23-50 years) attending Ninewells Assisted Conception Unit, Dundee for diagnostic semen analysis, July 2017-September 2018. Semen samples (n = 47) from 45 patients were used.
PARTICIPANTS/MATERIALS, SETTING, METHODS: Neutrophils activated using zymosan were incubated with prepared human spermatozoa for 2 h (T2) and 24 h (T24) to create an in vitro model of OS. Parallel samples were co-incubated with AZD5904, an MPOi, to examine its effects. Sperm motility was assessed by computer-assisted sperm analysis at T2 and T24. Functional motility was assessed by sperm penetration assay. Statistical analysis was performed using GraphPad Prism.
There was no significant difference in total or progressive sperm motility between any treatment and control groups at T2 or T24. Nonetheless, significant positive effects on sperm function were observed with AZD5904, with 16/45 (35.6%) samples (with both normal and abnormal baseline semen analysis characteristics) displaying a ≥20% increase in sperm penetrated through viscous media (P < 0.003).
LIMITATIONS, REASONS FOR CAUTION: This was an in vitro study.
Treatment with AZD5904 resulted in significant increased sperm penetration in one of three samples treated, which is likely to represent improvement in sperm function required for fertilization. We are now planning a clinical trial to validate these results and hope that this could represent a new treatment for male infertility.
STUDY FUNDING/COMPETING INTEREST(S): AZD5904 was shared through the AstraZeneca Open Innovation program. The study was funded by AstraZeneca and sponsored by the University of Dundee. Additional funding was provided by Chief Scientist Office/NHS Research Scotland (S.J.M.d.S.). A.W. and H.J.S. are both full time employees of AstraZeneca. A.W. and H.J.S. are inventors on a patent filed by AstraZeneca titled MPOi for use in medicine which includes MPOi for use in the treatment of male infertility (WO 2019/016074 Al). S.J.M.d.S. is Associate Editor of Human Reproduction and Editorial Board member of Reproduction & Fertility. C.L.R.B. is Editor of RBMO and has received lecturing fees from Merck and Ferring and is on the Scientific Advisory Panel for Ohana BioSciences. C.L.R.B. was chair of the World Health Organization Expert Synthesis Group on Diagnosis of Male infertility (2012-2016). C.L.R.B. has a patent WO2013054111 A1 issued. The other authors declare no conflict of interest.
N/A.
髓过氧化物酶抑制剂(MPOi)AZD5904 是否会对体外人类精子功能产生影响?
AZD5904 可改善氧化应激(OS)体外模型中的精子功能,为男性不育提供了一种新的潜在治疗方法。
男性不育是所有有生育困难的夫妇中一半以上的潜在或促成因素,但目前尚无有效的治疗或治愈方法。氧化应激是相当一部分不育男性的常见病理。它会对精子活力和使成熟卵受精的能力以及 DNA 完整性产生负面影响,因此代表了治疗干预的有吸引力的目标。
研究设计、大小、持续时间:本研究纳入了 2017 年 7 月至 2018 年 9 月期间在邓迪九井辅助受孕中心接受诊断性精液分析的男性(23-50 岁)的人群样本。使用了来自 45 名患者的 47 份精液样本。
参与者/材料、设置、方法:使用酵母聚糖激活中性粒细胞,与制备的人类精子在 2 小时(T2)和 24 小时(T24)孵育,以建立体外氧化应激模型。平行样本与 MPOi AZD5904 共孵育,以检查其效果。在 T2 和 T24 时通过计算机辅助精子分析评估精子活力。通过精子穿透试验评估功能运动。使用 GraphPad Prism 进行统计分析。
在 T2 或 T24 时,任何治疗组与对照组之间的总或渐进性精子活力均无显着差异。尽管如此,AZD5904 对精子功能仍有显着的积极影响,有 16/45(35.6%)个样本(具有正常和异常基线精液分析特征)显示精子穿透粘性介质的增加≥20%(P <0.003)。
局限性、谨慎的原因:这是一项体外研究。
AZD5904 的治疗导致三分之一治疗的样本中精子穿透显著增加,这可能代表受精所需的精子功能得到改善。我们现在正在计划一项临床试验来验证这些结果,并希望这能成为男性不育的一种新的治疗方法。
研究资金/利益冲突:AZD5904 通过阿斯利康开放创新计划共享。该研究由阿斯利康资助,并由邓迪大学赞助。额外的资金由首席科学家办公室/苏格兰 NHS 研究提供(SJMdS)。AW 和 HJS 均为阿斯利康的全职员工。AW 和 HJS 是阿斯利康提交的一项专利的发明者,该专利题为 MPOi 用于医学,其中包括 MPOi 用于治疗男性不育症(WO 2019/016074 Al)。SJMdS 是人类生殖的编辑委员会成员和生殖与生育的编辑委员会成员。CLRB 是 RBMO 的编辑,曾从默克和 Ferring 获得演讲费,并且是 Ohana BioSciences 的科学顾问小组的成员。CLRB 担任世界卫生组织男性不育症诊断专家综合组主席(2012-2016 年)。CLRB 拥有 WO2013054111 A1 号专利。其他作者均声明不存在利益冲突。
无。