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经牛卵母细胞胞浆内精子注射后正常犊牛的诞生:一种方法学途径。

Birth of normal calves after intracytoplasmic sperm injection of bovine oocytes: a methodological approach.

作者信息

Horiuch T, Emuta C, Yamauchi Y, Oikawa T, Numabe T, Yanagimachi R

机构信息

Department of Bioresources, Hiroshima Prefectural University, Shoubara, Japan.

出版信息

Theriogenology. 2002 Feb;57(3):1013-24. doi: 10.1016/s0093-691x(01)00701-4.

Abstract

Intracytoplasmic sperm injection (ICSI) is advantageous when only very few spermatozoa are available for insemination. Bovine spermatozoa were injected individually into matured oocytes using a piezo electric actuator. Spermatozoa were "immobilized", by scoring their tails immediately before injection, or "killed", by repeated freezing and thawing. About 4 h after ICSI, the oocytes with two polar bodies (activated by sperm injection) were selected and treated 5 min with 7% ethanol before further culture. When examined 19-21 h after ICSI, nearly 90% of the oocytes were fertilized normally (two pronuclei and two polar bodies) irrespective of the sperm treatment (immobilization or killing) prior to ICSI, but subsequent preimplantation embryo development was much superior (cleavage 72%: blastocysts 20%) after ICSI with immobilized spermatozoa than by using killed spermatozoa (cleavage 28%; blastocysts 1%). Ethanol activation of bovine oocytes with two polar bodies 4 h after ICSI improved the cleavage (33% versus 72%) and blastocyst (12% versus 20%) rates markedly (P < 0.05). Five normal calves were born after transplantation of ten blastocysts to ten surrogate cows. These results show that piezo-ICSI using immobilized spermatozoa, combined with ethanol treatment of sperm-injected oocytes, is an effective method to produce bovine offspring.

摘要

当仅有极少量精子可用于授精时,胞浆内单精子注射(ICSI)具有优势。使用压电驱动器将牛精子逐个注射到成熟卵母细胞中。精子在注射前通过划破其尾部使其“固定”,或通过反复冻融使其“失活”。ICSI后约4小时,选择排出两个极体(由精子注射激活)的卵母细胞,并用7%乙醇处理5分钟,然后进行进一步培养。在ICSI后19 - 21小时检查时,无论ICSI前精子的处理方式(固定或失活)如何,近90%的卵母细胞正常受精(出现两个原核和两个极体),但与使用失活精子的ICSI相比,使用固定精子的ICSI后胚胎植入前发育要好得多(卵裂率72%:囊胚率20%),而使用失活精子的ICSI卵裂率为28%,囊胚率为1%。ICSI后4小时用乙醇激活排出两个极体的牛卵母细胞,显著提高了卵裂率(33%对72%)和囊胚率(12%对20%)(P < 0.05)。将10个囊胚移植到10头代孕母牛后,产下了5头正常小牛。这些结果表明,使用固定精子的压电ICSI结合对注射精子的卵母细胞进行乙醇处理,是生产牛后代的一种有效方法。

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