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超氧化物歧化酶对小鼠植入前胚胎发育的影响。

Effect of superoxide dismutase on the development of preimplantation mouse embryos.

作者信息

Chun Y S, Kim J H, Lee H T, Chung K S

机构信息

Department of Animal Science, Animal Resources Research Center Kon-Kuk University, 93-1 Mojin-Dong, Seongdong-Ku, Seoul 133-701, Korea.

出版信息

Theriogenology. 1994 Feb;41(2):511-20. doi: 10.1016/0093-691x(94)90087-y.

Abstract

The role of superoxide dismutase (SOD) was tested on preimplantation development of mouse embryos in vitro. The presence of SOD in ovarian antral follicles and in oviductal and uterine secretions was also investigated. Zygotes from superovulated ICR female mice were cultured in modified Whittingham's T6 medium supplemented with SOD (0 to 370 U) or EDTA (100 muM) at 37 degrees C under 5% CO(2) in air. Supplementation of SOD (370 U) significantly promoted the development of zygotes to the blastocyst stage (45%) as compared to that of the controls (1.4%). This favorable effect of SOD was comparable to that of EDTA and completely suppressed by anti-SOD antibody. Blastocysts cultured with SOD consisted of 78.2+/-10.4 blastomeres and possessed as many blastomeres as those (81.6+/-9.3) developing in vivo; blastocysts cultured with EDTA had significantly fewer blastomeres (42.6+/-13.7). These findings suggest that SOD protects embryos against oxidative insults and that it can be an effective substitute for EDTA for supporting mouse embryo development in vitro. The SOD activity was detected in 3 different lumina from mouse reproductive organs, and SOD was identified as a cytosolic Cu,Zn-SOD on photochemically stained polyacrylamide gels. Our results suggest that oxidative injury may be responsible for developmental retardation of preimplantation-stage mouse embryos in vitro and that Cu,Zn-SOD may play a crucial role in protecting embryos against oxygen toxicity in vivo as well as in vitro.

摘要

研究了超氧化物歧化酶(SOD)在小鼠胚胎体外植入前发育中的作用。同时还研究了SOD在卵巢窦卵泡、输卵管和子宫分泌物中的存在情况。将超排ICR雌性小鼠的合子在添加了SOD(0至370 U)或EDTA(100 μM)的改良惠廷厄姆T6培养基中,于37℃、5%二氧化碳的空气中培养。与对照组(1.4%)相比,添加SOD(370 U)显著促进了合子发育至囊胚阶段(45%)。SOD的这种有利作用与EDTA相当,并被抗SOD抗体完全抑制。用SOD培养的囊胚由78.2±10.4个卵裂球组成,其卵裂球数量与体内发育的囊胚(81.6±9.3个)一样多;用EDTA培养的囊胚卵裂球数量明显较少(42.6±13.7个)。这些发现表明,SOD可保护胚胎免受氧化损伤,并且它可以作为EDTA的有效替代品,用于支持小鼠胚胎的体外发育。在小鼠生殖器官的3种不同腔液中检测到了SOD活性,并且在光化学染色的聚丙烯酰胺凝胶上鉴定SOD为胞质铜锌超氧化物歧化酶。我们的结果表明,氧化损伤可能是体外植入前阶段小鼠胚胎发育迟缓的原因,并且铜锌超氧化物歧化酶可能在体内和体外保护胚胎免受氧毒性方面发挥关键作用。

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