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

比较富血小板血浆和纳米姜黄素对弱精子症畸形男性冷冻解冻精液中精子质量参数的影响:一项实验室试验研究

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Abstract

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), PRP(50), PRP(100), nCur(10), and nCur(20). 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 PRP(50) (p  <  0.001) and nCur(20) (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 PRP(50) 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 PRP(50) 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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