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从新鲜样本估计解冻后牛精子的质量。

Post-thaw bovine spermatozoal quality estimated from fresh samples.

作者信息

Thomas C A, Garner D L

机构信息

School of Veterinary Medicine, University of Nevada, Reno 89557.

出版信息

J Androl. 1994 Sep-Oct;15(5):489-500.

PMID:7860431
Abstract

Comparisons were made among flow cytometrically quantified populations of fresh and cryopreserved bovine spermatozoa, tri-stained with fluorophores rhodamine 123 (R123), 5- (and 6-) carboxy-4',5'-dimethylfluorescein diacetate (CMFDA), and propidium iodide (PI), and analyzed by dual parameter flow cytometry. The purpose was to find parameters in fresh semen samples that were potentially predictive of frozen sample parameters so that bulls with marginal cryopreservation capacity could be identified. Fresh and cryopreserved aliquots of semen from two sets of six bulls were semen processed in either milk (bulls 1-6) or egg yolk citrate (bulls 11-16). Membrane-damaged red (PI) and intact green (CMFDA + R123) populations were evaluated as percentages of 10,000-cell samples or numbers per straw. In milk, gated central subsets of membrane-damaged sperm cells in fresh samples and moribund cells in post-thaw samples were significantly correlated for sample percentages (r = 0.90, P = 0.014) and cell numbers per straw (r = 0.94, P = 0.006). In egg yolk citrate, fresh and frozen membrane-damaged populations were correlated (percentages: r = 0.81, P = 0.048; numbers: r = 0.88, P = 0.019). Additionally, post-thaw motility estimated by a photographic method was correlated with the number of sperm cells per straw in the intact central green subset (r = 0.98, P = 0.0006). These findings suggest that partitioning red and gree populations into smaller, central subset populations reveals significant relationships between fresh and cryopreserved bull ejaculates. The proportion of membrane-damaged spermatozoa in fresh semen seems to be predictive of the proportion of post-thaw membrane-damaged or moribund spermatozoa. The data consistently showed ejaculates of bulls 1 and 12 as having the greatest cryopreservation potentials, and bulls 4 and 16 the least. Thus, flow cytometric evaluation of fresh semen may be useful for identifying young sires with relatively poor fertilizing potential.

摘要

对新鲜和冷冻保存的牛精子进行流式细胞术定量分析,用罗丹明123(R123)、5-(和6-)羧基-4',5'-二甲基荧光素二乙酸酯(CMFDA)和碘化丙啶(PI)进行三色染色,并通过双参数流式细胞术进行分析。目的是在新鲜精液样本中找到可能预测冷冻样本参数的参数,以便识别冷冻保存能力边缘的公牛。从两组六头公牛采集的新鲜和冷冻保存的精液等分试样,分别在牛奶(公牛1 - 6)或蛋黄柠檬酸盐(公牛11 - 16)中进行精液处理。膜受损的红色(PI)和完整的绿色(CMFDA + R123)群体按10,000个细胞样本的百分比或每支细管中的细胞数进行评估。在牛奶中,新鲜样本中膜受损精子细胞的门控中央亚群与解冻后样本中的濒死细胞在样本百分比(r = 0.90,P = 0.014)和每支细管中的细胞数(r = 0.94,P = 0.006)方面显著相关。在蛋黄柠檬酸盐中,新鲜和冷冻的膜受损群体相关(百分比:r = 0.81,P = 0.048;数量:r = 0.88,P = 0.019)。此外,通过摄影方法估计的解冻后活力与完整中央绿色亚群中每支细管中的精子细胞数相关(r = 0.98,P = 0.0006)。这些发现表明,将红色和绿色群体划分为更小的中央亚群揭示了新鲜和冷冻保存的公牛射精之间的显著关系。新鲜精液中膜受损精子的比例似乎可以预测解冻后膜受损或濒死精子的比例。数据一致显示公牛1和12的射精具有最大的冷冻保存潜力,而公牛4和16的潜力最小。因此,对新鲜精液进行流式细胞术评估可能有助于识别受精潜力相对较差的年轻种公牛。

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