Comar Vanessa A, Petersen Claudia G, Mauri Ana L, Mattila Mariana, Vagnini Laura D, Renzi Adriana, Petersen Bruna, Nicoletti Andreia, Dieamant Felipe, Oliveira Joao Batista A, Baruffi Ricardo L R, Franco José G
Center for Human Reproduction Prof. Franco Jr., Ribeirão Preto, SP, Brazil.
Paulista Center for Diagnosis Research and Training, Ribeirão Preto, SP, Brazil.
JBRA Assist Reprod. 2017 Dec 1;21(4):306-312. doi: 10.5935/1518-0557.20170052.
The aim of this study was to evaluate the influence of different periods of abstinence on conventional semen parameters as well as functional parameters in human semen, including mitochondrial function, chromatin packing and sperm DNA fragmentation.
We recruited a cohort of 2,458 men undergoing infertility investigation. Semen analyses were performed according to WHO guidelines/morphology-motile sperm organelle morphology examination/MSOME. For DNA integrity analysis, the percentages of DNA fragmentation (TUNEL), abnormal chromatin packaging/underprotamination (chromomycin A3/CMA3), abnormal mitochondrial membrane potential (MMP/MitoTracker Green), and apoptosis (annexin-V) were recorded. Associations between the sexual abstinence period and sperm parameters were assessed using Spearman correlation. For group comparisons, the subjects were categorized according to the sexual abstinence period (SAP) into three groups: SAP <2 days, SAP 2-5 days, and SAP >5 days.
The duration of abstinence had a statistically significant positive influence on sperm concentration and volume, the number of leukocytes and a statistically significant negative influence on sperm motility and vitality. The percentages of DNA fragmentation and MMP (mitochondrial damage) worsened with the increased duration of abstinence. The percentage of sperm protamination was statistically significantly increased with abstinence.
Increase in the sexual abstinence period influences sperm quality. This study reinforces the importance of the duration of ejaculatory abstinence on semen parameter variation. It highlights the deleterious effect of increased abstinence on DNA damage, which is most likely associated with ROS (mitochondrial damage/number of leukocytes). The increase in chromatin packaging can represent a protective feature for DNA.
本研究旨在评估不同禁欲期对人类精液常规参数以及功能参数的影响,包括线粒体功能、染色质包装和精子DNA片段化。
我们招募了2458名接受不孕症检查的男性。根据世界卫生组织指南/形态学-活动精子细胞器形态检查/MSOME进行精液分析。对于DNA完整性分析,记录DNA片段化(TUNEL)、染色质包装异常/鱼精蛋白不足(放线菌素A3/CMA3)、线粒体膜电位异常(MMP/线粒体追踪绿)和凋亡(膜联蛋白-V)的百分比。使用Spearman相关性评估性禁欲期与精子参数之间的关联。为了进行组间比较,根据性禁欲期(SAP)将受试者分为三组:SAP<2天、SAP 2-5天和SAP>5天。
禁欲时间对精子浓度和体积、白细胞数量有统计学显著的正向影响,对精子活力和存活率有统计学显著的负向影响。DNA片段化和MMP(线粒体损伤)的百分比随着禁欲时间的延长而恶化。精子鱼精蛋白的百分比随着禁欲而在统计学上显著增加。
性禁欲期的增加会影响精子质量。本研究强化了射精禁欲时间对精液参数变化的重要性。它突出了禁欲增加对DNA损伤的有害影响,这很可能与ROS(线粒体损伤/白细胞数量)有关。染色质包装的增加可能代表对DNA的一种保护特征。