特发性男性不育症内皮素受体表达改变:一个潜在的治疗靶点。

0 UROLOGY & NEPHROLOGY
Richard Weiten, Melanie V Brandenstein, Manuel Huerta, Tim Nestler, Axel Heidenreich, Enno Storz, Jan Herden
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引用次数: 0

摘要

目的:特发性男性不育症通常与精液质量受损有关,特别是在诊断为少弱畸形精子症(OAT)综合征的男性中。最近的研究表明,内皮素(ET)系统,特别是ET受体a (ETAR)和B (ETBR)在男性生殖生理中的潜在作用。此外,抗雌激素,如他莫昔芬和克罗米芬,在这种情况下通常使用的经验,可能会影响ET信号通路。然而,ET受体表达与男性不育症特定亚型之间的关系仍然知之甚少。方法:采集56例男性的精液样本,其中正常精子症可育者15例,精液参数异常的不育者41例,其中OAT综合征22例,孤立性畸形精子症19例。排除有明确女性因素导致的不孕症的男性。采用免疫荧光显微镜、Western blotting、酶联免疫抗体弯曲试验(ELISA)和流式细胞术分析种子ETAR和ETBR的表达。结果:与有生育能力的对照组相比,不育男性的ETAR表达明显降低(P < 0.05)。在OAT综合征患者的所有样本中均未检测到ETBR。值得注意的是,在OAT组中观察到2种不同的ETAR表达谱:一个亚组的ETAR水平与对照组相当,另一个亚组的ETAR表达明显降低,这表明OAT综合征中潜在的表型异质性。结论:特发性不育症患者,特别是OAT综合征患者,ETAR表达改变和ETBR缺失,突出了ET信号在男性生殖功能障碍中的潜在作用。基于ETAR表达的分层可能支持个体化治疗策略,包括以et为目标或以抗雌激素为基础的治疗,以改善这一人群的生育结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Altered Endothelin Receptor Expression in Idiopathic Male Infertility: A Potential Therapeutic Target.

Objective: Idiopathic male infertility is frequently associated with impaired semen quality, particularly in men diagnosed with oligo-astheno-teratozoospermia (OAT) syn- drome. Recent studies suggest a potential role of the endothelin (ET) system, particu- larly ET receptors A (ETAR) and B (ETBR), in male reproductive physiology. Moreover, antiestrogens such as tamoxifen and clomiphene, which are commonly used empiri- cally in this context, may influence ET signaling pathways. However, the relationship between ET receptor expression and specific subtypes of male infertility remains poorly understood. Methods: Semen samples were collected from 56 men: 15 fertile controls with normo- zoospermia and 41 infertile men with abnormal semen parameters, including 22 with OAT syndrome and 19 with isolated teratozoospermia. Men with identifiable female- factor infertility were excluded. Seminal ETAR and ETBR expression were analyzed using immunofluorescence microscopy, Western blotting, enzyme-linked immunosor- bent assay (ELISA), and flow cytometry. Results: The ETAR expression was significantly reduced in infertile men compared to fertile controls (P < .05). The ETBR was undetectable in all samples from patients with OAT syndrome. Notably, 2 distinct ETAR expression profiles were observed within the OAT group: one subgroup with ETAR levels comparable to controls and another with markedly diminished expression, indicating potential phenotypic heterogeneity within OAT syndrome. Conclusion: Altered ETAR expression and the absence of ETBR in men with idiopathic infertility, particularly those with OAT syndrome, highlight a potential role for ET sig- naling in male reproductive dysfunction. Stratification based on ETAR expression may support individualized therapeutic strategies, including ET-targeted or antiestrogen- based therapies, to improve fertility outcomes in this population.

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