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Improved cryopreservation of domestic cat sperm in a chemically defined medium

机译:在化学成分确定的培养基中改进了家猫精子的冷冻保存

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The objective was to compare a proprietary egg yolk-based cryopreservation medium with a chemically defined soy-based medium, as well as to examine effects of temperature of glycerol addition on sperm parameters and IVF after freezing and thawing of domestic cat sperm. Semen was collected from adult cats (four males and three ejaculates per male), divided in four equal aliquots, and extended in either egg yolk with 4% glycerol added before (EYG) or after (EY) cooling to 5 degrees C, or soy-lecithin with 4% glycerol added before (SLG) or after (SL) cooling to 5 degrees C. Extended sperm were frozen in straws over liquid nitrogen vapor. Sperm progressive motility (%) and rate of progressive movement (scale of 0-5) were evaluated at 0, 1, 3, 6, and 24 h post-thaw. Sperm capacitation, acrosome integrity, and DNA integrity were assessed at 15 min post-thaw. Effects of media (EY or SL) on IVF success was also examined (three males and three ejaculates per male). Sperm motility was greater (P<0.05) in soy-based compared with egg yolk-based media at 3, 6, and 24 h post-thaw. A higher (P<0.05) percentage of noncapacitated sperm (pattern F) were present in soy-based (SLG, 63.7+or-9.2%; and SL, 64.1+or-9.2%) compared with egg yolk-based (EYG, 49.9+or-7.9%; and EY, 52.4+or-18.6%) cryopreservation media, regardless of temperature of glycerol addition. Addition of glycerol at 5 degrees C increased (P<0.05) percentage of sperm motility at 6 h (EYG 16.3+or-8.3% vs. EY, 24.0+or-11.7%; SLG, 36.7+or-6.5% vs. SL, 42.9+or-10.1%) and 24 h (EYG, 2.1+or-3.3% vs. EY, 8.3+or-3.9%; SLG, 11.3+or-8.3% vs. SL, 18.8+or-7.4%) post-thaw in both media. There were no differences (P>0.05) between cryodiluents in embryo cleavage, percentage of embryos reaching blastocyst, or cell number per blastocyst. The chemically defined, soy-based medium resulted in better preservation of long-term motility and capacitation status of frozen-thawed domestic cat sperm compared with a commercial egg yolk-based extender, without compromising fertilizing ability.
机译:目的是将专有的基于蛋黄的冷冻保存培养基与化学成分确定的基于大豆的培养基进行比较,并检查甘油的添加温度对家猫精子冷冻和解冻后对精子参数和IVF的影响。从成年猫中收集精液(四只雄性,每只雄性三只射精),分成四等份,并在蛋黄中加4%甘油,然后在冷却至5摄氏度(EYG)之前或之后(EY)进行扩展,或者添加大豆(SLG)之前或之后(SL)冷却至5摄氏度后,添加含4%甘油的β-卵磷脂。将精子在液氮蒸气中用吸管冷冻。在解冻后0、1、3、6和24 h评估精子的进行性运动(%)和进行性运动的速度(0-5级)。解冻后15分钟评估精子获能,顶体完整性和DNA完整性。还检查了媒介(EY或SL)对IVF成功的影响(三名男性,每名男性三个射精)。解冻后3、6和24小时,与基于蛋黄的培养基相比,基于大豆的精子活动性更大(P <0.05)。与基于蛋黄的蛋黄(EYG)相比,基于大豆的(SLG,63.7 +或-9.2%; SL,64.1 +或-9.2%)的无能精子(模式F)百分比更高(P <0.05)。 49.9%或-7.9%;和EY,52.4%或18.6%的冷冻保存介质,与添加甘油的温度无关。在5°C时添加甘油会增加(h P <0.05)6 h精子运动百分比(EYG 16.3+或-8.3%vs. EY,24.0+或-11.7%; SLG,36.7+或-6.5%vs.SL ,42.9 +或-10.1%)和24小时(EYG,2.1%或-3.3%vs.EY,8.3+或-3.9%; SLG,11.3+或-8.3%vs SL,18.8+或-7.4%)在两种媒体中解冻。冷冻稀释剂在胚胎裂解,到达胚泡的胚百分比或每个胚泡的细胞数之间没有差异(P> 0.05)。与基于蛋黄的市售补充剂相比,基于化学成分的基于大豆的培养基可更好地保留冻融的家养猫精子的长期运动性和获能状态,而不会影响施肥能力。

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