精液化学的简单测试及其对冷冻保存的潜在影响

Glenn Yeomans, Lindsay Penrose, Sam Prien
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引用次数: 0

摘要

低温保存是目前大多数物种精液长期保存的唯一有效工具。然而,众所周知的是,即使在冷冻良好的物种中,一些个体也会抵抗冷冻保存。这个实验室的工作已经证明了母体的脂质含量和它们所产生的胚胎的化学构成之间的关系。本研究的目的是确定父系身体化学和动物精液样本之间是否存在类似的关系,以及这种差异是否可以通过简单的体重测试来确定。精液样本取自身体成分已知差异的牛。样品首先进行精液分析,然后制备无细胞(CF)或整齐标本(NS)。对每个样品的已知体积进行称重,并使用一系列分光光度法和血液化学技术分析剩余样品的脂质,总蛋白质和总碳水化合物。正如预期的那样,在单个精液样本的CF和NS制剂中发现了体重差异(p < 0.001)。不同身体组成的个体在甘油三酯(p < 0.001)、葡萄糖(p < 0.001)、总蛋白(p < 0.001)和果糖(p < 0.009)方面也存在差异。统计分析表明,体重与总蛋白(p < 0.047)和甘油三酯水平(p < 0.003)呈非线性相关。总之,这些数据表明,有可能开发出一种算法,允许基于简单的称重程序调整冷冻保护剂,允许在个体基础上修改冷冻保护剂,并有可能改善目前被归类为“不良冷冻”的珍贵动物的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Simple Test of Seminal Fluid Chemistry and Its Potential Impact on Cryopreservation
Cryopreservation is currently the only effective tool for long-term storage of semen in most species. However, it is well-recognized that, even in species that freeze well, some individuals resist cryopreservation. Work from this laboratory has demonstrated a relationship between maternal lipid content and the chemical constitution of the embryos they produce. The objective of the present study was to determine if a similar relationship might exist in paternal body chemistry and the animal’s semen sample and if such a difference could be determined with a simple weight test. Semen samples were obtained from cattle with known differences in body composition. The samples first underwent semen analysis and were then prepared as either cell-free (CF) or neat specimens (NS). Known volumes of each sample were weighed, and the remainder of the samples was analyzed for lipids, total proteins, and total carbohydrates using a series of spectrophotometric assays and blood chemistry techniques. As expected, weight differences were seen in the CF vs NS preparations of individual semen samples (p < 0.001). Differences were also found in triglycerides (p < 0.001), glucose (p < 0.001), total protein (p < 0.001), and fructose (p < 0.009) of individuals with differing body composition. Statistical analysis suggested a non-linear correlation between the observed weights and total protein (p < 0.047) as well as triglyceride levels (p < 0.003). Together, these data suggest it might be possible to develop an algorithm to allow adjustment in cryoprotectants based on a simple weight procedure, allowing modification of cryoprotectants on an individual basis and potentially improving outcomes for valuable animals currently classified as “poor freezers”.
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