Nagai T, Takenaka A, Mori T, Hirayama M
Department of Animal Production, Tohoku National Agricultural Experiment Station, Iwate, Japan.
Mol Reprod Dev. 1994 Apr;37(4):452-6. doi: 10.1002/mrd.1080370412.
Two experiments were conducted to assess the effects of caffeine and casein phosphopeptides (CPPs). One experiment tested the ability of frozen-thawed epididymal spermatozoa from boar (A, B, C), of proven low in vitro fertilization rates, to penetrate pig follicular oocytes. The other experiment tested the ability of ejaculated spermatozoa to uptake Ca2+. In Experiment 1, oocytes matured in vitro were inseminated with spermatozoa (Boar A) in medium that contained 0, 2, 5, 10, 15, and 20 mM caffeine and CPPs (1 mg/ml), or in medium that contained the same caffeine concentrations without CPPs. When CPPs were added to the caffeine-containing medium, significantly higher penetration rates were obtained than when the oocytes were inseminated in the CPPs-free medium. When the oocytes were inseminated with the spermatozoa (Boar A, B, C) in medium that contained 5 mM caffeine and dephosphorylated CPPs (dCPP:1 mg/ml), the penetration rate was significantly lower than when the oocytes were inseminated with the spermatozoa in medium containing 5 mM caffeine and CPPs (1 mg/ml). In Experiment 2, the concentration of Ca2+ in ejaculated spermatozoa of proven low in vitro fertilization rates during incubation in the fertilization medium was determined with fluorescence, Fura2/AM. When the medium contained CPPs, the intracellular concentration of Ca2+ in spermatozoa increased with a peak of 113 nM after 90 min of incubation. The concentration of Ca2+ was gradually decreased in the medium without CPPs. However, addition of CPPs in the medium had no effect on the motility of spermatozoa in Experiments 1 and 2.(ABSTRACT TRUNCATED AT 250 WORDS)
进行了两项实验来评估咖啡因和酪蛋白磷酸肽(CPPs)的作用。一项实验测试了来自体外受精率经证实较低的公猪(A、B、C)的冻融附睾精子穿透猪卵泡卵母细胞的能力。另一项实验测试了射出精子摄取Ca2+的能力。在实验1中,将体外成熟的卵母细胞与精子(公猪A)在含有0、2、5、10、15和20 mM咖啡因以及CPPs(1 mg/ml)的培养基中进行受精,或者在含有相同咖啡因浓度但不含CPPs的培养基中进行受精。当将CPPs添加到含咖啡因的培养基中时,与在不含CPPs的培养基中受精的卵母细胞相比,获得了显著更高的穿透率。当卵母细胞与精子(公猪A、B、C)在含有5 mM咖啡因和去磷酸化CPPs(dCPP:1 mg/ml)的培养基中受精时,穿透率显著低于在含有5 mM咖啡因和CPPs(1 mg/ml)的培养基中受精的卵母细胞。在实验2中,使用荧光染料Fura2/AM测定了体外受精率经证实较低的射出精子在受精培养基中孵育期间Ca2+的浓度。当培养基中含有CPPs时,精子细胞内Ca2+浓度在孵育90分钟后升高,峰值为113 nM。在不含CPPs的培养基中,Ca2+浓度逐渐降低。然而,在实验1和实验2中,向培养基中添加CPPs对精子活力没有影响。(摘要截断于250字)