Zhang T, Wang R Y, Bao Q-Y, Rawson D M
Luton Institute of Research in the Applied Natural Sciences, University of Luton, The Spires, 2 Adelaide Street, Luton, Bedfordshire LU1 5DU, UK.
Theriogenology. 2006 Sep 1;66(4):982-8. doi: 10.1016/j.theriogenology.2006.02.038. Epub 2006 Apr 3.
Information on fish embryo membrane permeability is vital in their cryopreservation. Whilst conventional volumetric measurement based assessment methods have been widely used in fish embryo membrane permeability studies, they are lengthy and reduce the capacity for multi-embryo measurement during an experimental run. A new rapid 'real-time' measurement technique is required to determine membrane permeability during cryoprotectant treatment. In this study, zebrafish (Danio rerio) embryo membrane permeability to cryoprotectants was investigated using impedance spectroscopy. An embryo holding cell, capable of holding up to 10 zebrafish embryos was built incorporating the original system electrods for measuring the impedance spectra. The holding cell was tested with deionised water and a series of KCl solutions with known conductance values to confirm the performance of the modified system. Untreated intact embryos were then tested to optimise the loading capacity and sensitivity of the system. To study the impedance changes of zebrafish embryos during cryoprotectant exposure, three, six or nine embryos at 50% epiboly stage were loaded into the holding cell in egg water, which was then removed and replaced by 0.5, 1.0, 2.0 or 3M methanol or dimethyl sulfoxide (DMSO). The impedance changes of the loaded embryos in different cryoprotectant solutions were monitored over 30 min at 22 degrees C, immediately following embryo exposure to cryoprotectants, at the frequency range of 10-10(6)Hz. The impedance changes of the embryos in egg water were used as controls. Results from this study showed that the optimum embryo loading level was six embryos per cell for each experimental run. The optimum frequency was identified at 10(3.14) or 1,380 Hz which provided good sensitivity and reproducibility. Significant impedance changes were detected after embryos were exposed to different concentrations of cryoprotectants. The results agreed well with those obtained from conventional volumetric based studies.
鱼类胚胎膜通透性的信息对于其冷冻保存至关重要。虽然基于传统体积测量的评估方法已广泛应用于鱼类胚胎膜通透性研究,但这些方法耗时较长,且在实验过程中降低了多胚胎测量的能力。需要一种新的快速“实时”测量技术来确定冷冻保护剂处理过程中的膜通透性。在本研究中,使用阻抗谱研究了斑马鱼(Danio rerio)胚胎膜对冷冻保护剂的通透性。构建了一个能够容纳多达10个斑马鱼胚胎的胚胎容纳池,该容纳池结合了用于测量阻抗谱的原始系统电极。用去离子水和一系列已知电导率值的KCl溶液对容纳池进行测试,以确认改进系统的性能。然后对未处理的完整胚胎进行测试,以优化系统的加载能力和灵敏度。为了研究斑马鱼胚胎在暴露于冷冻保护剂期间的阻抗变化,将处于50%外包期的3个、6个或9个胚胎放入盛有卵水的容纳池中,然后去除卵水,并用0.5M、1.0M、2.0M或3M的甲醇或二甲基亚砜(DMSO)替换。在胚胎暴露于冷冻保护剂后,立即在22摄氏度下,在10 - 10(6)Hz的频率范围内,对不同冷冻保护剂溶液中加载的胚胎的阻抗变化进行30分钟的监测。将胚胎在卵水中的阻抗变化用作对照。本研究结果表明,每次实验运行的最佳胚胎加载水平为每个细胞6个胚胎。确定的最佳频率为10(3.14)或1380Hz,该频率具有良好的灵敏度和可重复性。胚胎暴露于不同浓度的冷冻保护剂后检测到显著的阻抗变化。结果与基于传统体积测量的研究结果吻合良好。