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重组胰蛋白酶与猪胰提取物在用于体外生产牛胚胎的精子上的比较。

Comparison of a recombinant trypsin with the porcine pancreatic extract on sperm used for the in vitro production of bovine embryos.

作者信息

Mattson K J, Devlin B R, Loskutoff N M

机构信息

The Bill and Bernice Grewcock Center for Conservation and Research, Omaha's Henry Doorly Zoo, NE 68107-2200, USA.

出版信息

Theriogenology. 2008 Apr 1;69(6):724-7. doi: 10.1016/j.theriogenology.2007.11.018. Epub 2008 Feb 15.

Abstract

The objective was to compare the effects of treating bovine semen with two trypsin products (the porcine pancreas extract and a recombinant) and a control (no trypsin) on in vitro embryo production. Our hypothesis was that the trypsin treatments would not cause any significant difference in fertilization and embryo development as compared to the control. Semen was washed through a gradient system containing a porcine-origin trypsin, a recombinant bovine-sequence trypsin, or the control (no trypsin). Oocytes (n=3036) were collected from abbatoir-derived ovaries, matured for 24h, and allocated into three groups: porcine trypsin (n=1040), recombinant trypsin (n=972), and control (n=1024). Ova were inseminated with 1 x 10(6) motile sperm/mL and cultured for 18-24h. Thereafter, presumptive zygotes were cultured for 7 days in 50 microL G1/G2 micro-droplets under mineral oil. Overall, sperm motility was lower before than after each treatment (mean of 51.4% versus 70.2%, respectively; P<0.001); however, motility was not significantly different among the three groups (porcine-origin trypsin=68.8%, recombinant trypsin=69.0%, and control=72.6%). Similarly, there was no significant difference among these groups for cleavage rates (70.1, 70.9, and 73.9%), or the number of morula/blastocyst stage embryos (53.4, 53.3, and 48.7%). In conclusion, treatment of bovine sperm with either porcine-origin trypsin or recombinant trypsin prior to insemination had no detrimental effects on in vitro embryo development.

摘要

目的是比较两种胰蛋白酶产品(猪胰腺提取物和重组胰蛋白酶)以及一种对照(无胰蛋白酶)处理牛精液对体外胚胎生产的影响。我们的假设是,与对照相比,胰蛋白酶处理在受精和胚胎发育方面不会导致任何显著差异。精液通过含有猪源胰蛋白酶、重组牛序列胰蛋白酶或对照(无胰蛋白酶)的梯度系统洗涤。从屠宰场获取的卵巢中收集卵母细胞(n = 3036),培养24小时,然后分为三组:猪胰蛋白酶组(n = 1040)、重组胰蛋白酶组(n = 972)和对照组(n = 1024)。用每毫升1×10(6)个活动精子对卵子进行授精,并培养18 - 24小时。此后,将推定的受精卵在矿物油下的50微升G1/G2微滴中培养7天。总体而言,每次处理前精子活力低于处理后(分别为51.4%和70.2%;P<0.001);然而,三组之间的活力没有显著差异(猪源胰蛋白酶组 = 68.8%,重组胰蛋白酶组 = 69.0%,对照组 = 72.6%)。同样,这些组在分裂率(70.1%、70.9%和73.9%)或桑葚胚/囊胚阶段胚胎数量(53.4%、53.3%和48.7%)方面也没有显著差异。总之,授精前用猪源胰蛋白酶或重组胰蛋白酶处理牛精子对体外胚胎发育没有不利影响。

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