Boersma Auke, Olszanska Olga, Walter Ingrid, Rülicke Thomas
Institute of Laboratory Animal Science and Biomodels, University of Veterinary Medicine Vienna, Vienna, Austria.
VetCore Facility for Research, VetBiobank Unit, and Institute of Anatomy, Histology, and Embryology, University of Veterinary Medicine Vienna, Vienna, Austria.
J Am Assoc Lab Anim Sci. 2015 Sep;54(5):471-7.
Spermatozoa for in vitro fertilization of mouse oocytes and other methods of assisted reproduction typically are collected from the cauda epididymis of euthanized male mice. As an alternative to this terminal protocol, we developed and examined 2 methods for collecting sperm from anesthetized male mice without decreasing subsequent fertility: microsurgical epididymal sperm aspiration and, as a refinement, percutaneous epididymal sperm aspiration. Collected sperm was evaluated in terms of motility, concentration and in vitro fertilization ability. After recovery, both treated and untreated control male mice underwent in vivo fertility testing and subsequent histologic analysis of the treated male reproductive tract (epididymis and testis). In vitro fertilization using sperm recovered by the 2 collection methods was successfully achieved in all cases. The in vivo fertility test and the histologic analysis revealed no impairment of fertility and no permanent histologic alteration in the treated mice. Therefore, we recommend both techniques as simple and effective methods for recovering high-quality epididymal mouse sperm without having to euthanize fertile male mice.
用于小鼠卵母细胞体外受精及其他辅助生殖方法的精子通常从安乐死雄性小鼠的附睾尾部采集。作为这种终末方案的替代方法,我们开发并研究了两种在不降低后续生育力的情况下从麻醉雄性小鼠采集精子的方法:显微外科附睾精子抽吸术,以及作为改进的经皮附睾精子抽吸术。对采集的精子进行活力、浓度和体外受精能力评估。恢复后,对处理过的和未处理的对照雄性小鼠进行体内生育力测试,并对处理过的雄性生殖道(附睾和睾丸)进行后续组织学分析。使用通过这两种采集方法回收的精子成功实现了体外受精。体内生育力测试和组织学分析显示,处理过的小鼠生育力未受损,也没有永久性组织学改变。因此,我们推荐这两种技术作为简单有效的方法,用于在不必安乐死可育雄性小鼠的情况下回收高质量的附睾小鼠精子。