富血小板血浆和纳米姜黄素对弱异精子症男性冻融精液中精子质量参数影响的比较:实验室试验研究。

IF 1.8 Q3 OBSTETRICS & GYNECOLOGY
International Journal of Reproductive Biomedicine Pub Date : 2025-08-27 eCollection Date: 2025-07-01 DOI:10.18502/ijrm.v23i7.19481
Mahsa Soltani, Elham Shojafar, Ali Asghar Ghafarizadeh, Azam Moslemi, Farideh Jalali Mashayekhi, Maryam Baazm
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引用次数: 0

摘要

背景:精子低温保存会对精子质量产生不利影响,特别是对弱异精子症患者。在低温保存培养基中加入各种物质以防止细胞损伤。目的:本研究旨在评价富血小板血浆(PRP)和纳米姜黄素(nCur)对冷冻精液中精子参数、DNA断裂和氧化应激水平的影响。材料和方法:在本实验室试验研究中,收集了2024年6 - 8月在伊朗阿拉克的Rastak和Ghavamzadeh不育中心就诊的20名弱异卵精子症男性的精液样本。每个样本分为5组:对照组(未处理)、PRP50组、PRP100组、nCur10组和nCur20组。对照样品在不添加添加剂的情况下进行冷冻。解冻后评估包括精子活力、活力、DNA断裂指数和丙二醛水平,以评估氧化应激。结果:与对照组相比,PRP50 (p = 0.001)和nCur20 (p = 0.001)治疗显著提高了精子活力。所有治疗组均显示冷冻后活精子数量显著增加(p 0.001), PRP50表现出最显著的效果(p 0.001)。虽然冷冻后精子形态没有改善,但PRP和nCur显著降低了冷冻后的DNA片段化指数(p 0.001),其中PRP50最有效(p 0.001)。此外,与对照组相比,PRP和nCur均显著降低丙二醛水平(p 0.001)。结论:PRP和nCur能有效改善弱异精子症患者冷冻精液中的精子参数,尤其强调了PRP浓度为50时改善精子质量的优越性。这些结果支持这些药物作为精子冷冻保存方案添加剂的潜在用途,以改善生殖结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Comparison of the effects of platelet-rich plasma and nanocurcumin on the sperm quality parameters in frozen-thawed semen of men with asthenoteratozoospermia: A lab trial study.

Comparison of the effects of platelet-rich plasma and nanocurcumin on the sperm quality parameters in frozen-thawed semen of men with asthenoteratozoospermia: A lab trial study.

Comparison of the effects of platelet-rich plasma and nanocurcumin on the sperm quality parameters in frozen-thawed semen of men with asthenoteratozoospermia: A lab trial study.

Comparison of the effects of platelet-rich plasma and nanocurcumin on the sperm quality parameters in frozen-thawed semen of men with asthenoteratozoospermia: A lab trial study.

Background: Cryopreservation of sperm can adversely affect sperm quality, particularly in individuals with asthenoteratozoospermia. Various substances are added to the cryopreservation medium to prevent cellular damage.

Objective: This study aimed to evaluate the effects of platelet-rich plasma (PRP) and nanocurcumin (nCur) on sperm parameters, DNA fragmentation, and oxidative stress levels in cryopreserved semen.

Materials and methods: In this lab trial study, semen samples of 20 men with asthenoteratozoospermia who referred to Rastak and Ghavamzadeh Infertility Centers, Arak, Iran from June-August 2024 were collected. Each sample was divided into 5 groups: control (no treatment), PRP50, PRP100, nCur10, and nCur20. The control samples underwent freezing without additives. Post-thawing assessments included sperm motility, viability, DNA fragmentation index, and malondialdehyde levels to evaluate oxidative stress.

Results: Treatment with PRP50 (p < 0.001) and nCur20 (p = 0.001) significantly increased sperm motility compared to the control group. All treatment groups showed a significant increase in viable sperm following freezing (p < 0.001), with PRP50 demonstrating the most pronounced effects (p < 0.001). While no improvements in sperm morphology were observed after freezing, PRP and nCur significantly reduced DNA fragmentation index after freezing (p < 0.001), with PRP50 being the most effective (p < 0.001). Additionally, both PRP and nCur significantly decreased malondialdehyde levels compared to the control group (p < 0.001).

Conclusion: PRP and nCur effectively improve sperm parameters in cryopreserved semen from individuals with asthenoteratozoospermia, particularly emphasizing the superior efficacy of PRP at a concentration of 50 in improving sperm quality. These results support the potential use of these agents as additives in sperm cryopreservation protocols to improve reproductive outcomes.

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来源期刊
CiteScore
2.40
自引率
7.70%
发文量
93
审稿时长
16 weeks
期刊介绍: The International Journal of Reproductive BioMedicine (IJRM), formerly published as "Iranian Journal of Reproductive Medicine (ISSN: 1680-6433)", is an international monthly scientific journal for who treat and investigate problems of infertility and human reproductive disorders. This journal accepts Original Papers, Review Articles, Short Communications, Case Reports, Photo Clinics, and Letters to the Editor in the fields of fertility and infertility, ethical and social issues of assisted reproductive technologies, cellular and molecular biology of reproduction including the development of gametes and early embryos, assisted reproductive technologies in model system and in a clinical environment, reproductive endocrinology, andrology, epidemiology, pathology, genetics, oncology, surgery, psychology, and physiology. Emerging topics including cloning and stem cells are encouraged.
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