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在体连续采样小鼠附睾精子。

In vivo serial sampling of epididymal sperm in mice.

机构信息

Laboratorio de Criopreservación, Servicio de Experimentación Animal UMH, Instituto de Neurociencias de Alicante, Consejo Superior de Investigaciones Científicas/Universidad Miguel Hernández, Avenida Ramón y Cajal s/n, San Juan de Alicante, 03550 Alicante, Spain.

出版信息

Lab Anim. 2013 Jul;47(3):168-74. doi: 10.1177/0023677213478411.

Abstract

This study was undertaken to refine the techniques of in vivo collection of sperm in the mouse. The principal objective was to offer a viable, safe and reliable method for serial collection of in vivo epididimary sperm through the direct puncture of the epididymis. Six C57Bl/6J males were subjected to the whole experiment. First we obtain a sperm sample of the right epididymis, and perform a vasectomy on the left side. This sample was used in an in vitro fertilization (IVF) experiment while the males were individually housed for 10 days to let them recover from the surgery, and then their fertility was tested with natural matings until we obtained a litter of each one. After that, the animals were subjected another time to the same process (sampling, recover and natural mating). The results of these experiments were a fertilization average value of 56.7%, and that all the males had a litter in the first month after the natural matings. This study documented the feasibility of the epididimary puncture technique to in vivo serial sampling of sperm in the mouse.

摘要

本研究旨在完善体内采集小鼠精子的技术。主要目的是提供一种可行、安全、可靠的方法,通过直接穿刺附睾对附睾内精子进行连续采集。六只 C57Bl/6J 雄性被用于整个实验。首先,我们从右侧附睾中获取精子样本,并对左侧进行输精管切除术。该样本用于体外受精(IVF)实验,同时雄性被单独饲养 10 天,让它们从手术中恢复,然后进行自然交配以测试它们的生育能力,直到每只雄性都产下一窝幼崽。之后,这些动物再次经历相同的过程(采样、恢复和自然交配)。这些实验的结果是受精平均值为 56.7%,并且所有雄性在自然交配后的第一个月都产下了一窝幼崽。本研究证明了附睾穿刺技术在体内连续采集小鼠精子的可行性。

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