扬州大学学报(农业与生命科学版)
颺州大學學報(農業與生命科學版)
양주대학학보(농업여생명과학판)
JOURNAL OF YANGZHOU UNIVERSITY(AGRICULTURAL AND LIFE SCIENCE EDITION)
2009年
3期
41-44
,共4页
袁玉国%李锋%郭磊%缪明星%冯亚杰%柏亚军%成勇
袁玉國%李鋒%郭磊%繆明星%馮亞傑%柏亞軍%成勇
원옥국%리봉%곽뢰%무명성%풍아걸%백아군%성용
小鼠%胚胎%体外培养%程序化冷冻
小鼠%胚胎%體外培養%程序化冷凍
소서%배태%체외배양%정서화냉동
mouse%embryo%in vitro culture%programmed freezing
取小鼠原核(220枚)、2~4细胞胚胎(227枚)、桑椹胚(127枚),将其分为3组,每一时期胚胎分成两半,一半取出后立即冷冻复苏并体外培养至囊胚,另一半体外培养至囊胚后冷冻复苏,子宫冲取囊胚(78枚)冷冻复苏为对照组;各组囊胚均移植至于宫,比较程序化冷冻对小鼠早期胚胎存活率的影响.结果表明:原核、2~4细胞胚胎、桑椹胚体外培养至囊胚后冷冻复苏率分别为56.4%、72.2%、81.6%,移植产仔率分别为38.1%、41.6%、56.8%,原核、2~4细胞组复苏率和产仔率极显著或显著低于对照组,桑椹胚组与对照组差异不显著,显示体外培养对早期胚胎冷冻存活有影响;原核、2~4细胞胚胎、桑椹胚冷冻后体外培养至囊胚,胚胎移植后产仔率分别为25.3%、28.2%、42.1%,与对应胚胎时期体外培养至囊胚冷冻复苏后移植产仔率相比,原核、2~4细胞组均存在显著差异,而桑椹胚组差异不显著,显示原核、2~4细胞的早期胚胎体外培养至囊胚后冷冻可提高冷冻存活率.
取小鼠原覈(220枚)、2~4細胞胚胎(227枚)、桑椹胚(127枚),將其分為3組,每一時期胚胎分成兩半,一半取齣後立即冷凍複囌併體外培養至囊胚,另一半體外培養至囊胚後冷凍複囌,子宮遲取囊胚(78枚)冷凍複囌為對照組;各組囊胚均移植至于宮,比較程序化冷凍對小鼠早期胚胎存活率的影響.結果錶明:原覈、2~4細胞胚胎、桑椹胚體外培養至囊胚後冷凍複囌率分彆為56.4%、72.2%、81.6%,移植產仔率分彆為38.1%、41.6%、56.8%,原覈、2~4細胞組複囌率和產仔率極顯著或顯著低于對照組,桑椹胚組與對照組差異不顯著,顯示體外培養對早期胚胎冷凍存活有影響;原覈、2~4細胞胚胎、桑椹胚冷凍後體外培養至囊胚,胚胎移植後產仔率分彆為25.3%、28.2%、42.1%,與對應胚胎時期體外培養至囊胚冷凍複囌後移植產仔率相比,原覈、2~4細胞組均存在顯著差異,而桑椹胚組差異不顯著,顯示原覈、2~4細胞的早期胚胎體外培養至囊胚後冷凍可提高冷凍存活率.
취소서원핵(220매)、2~4세포배태(227매)、상심배(127매),장기분위3조,매일시기배태분성량반,일반취출후립즉냉동복소병체외배양지낭배,령일반체외배양지낭배후냉동복소,자궁충취낭배(78매)냉동복소위대조조;각조낭배균이식지우궁,비교정서화냉동대소서조기배태존활솔적영향.결과표명:원핵、2~4세포배태、상심배체외배양지낭배후냉동복소솔분별위56.4%、72.2%、81.6%,이식산자솔분별위38.1%、41.6%、56.8%,원핵、2~4세포조복소솔화산자솔겁현저혹현저저우대조조,상심배조여대조조차이불현저,현시체외배양대조기배태냉동존활유영향;원핵、2~4세포배태、상심배냉동후체외배양지낭배,배태이식후산자솔분별위25.3%、28.2%、42.1%,여대응배태시기체외배양지낭배냉동복소후이식산자솔상비,원핵、2~4세포조균존재현저차이,이상심배조차이불현저,현시원핵、2~4세포적조기배태체외배양지낭배후냉동가제고냉동존활솔.
The three different development stages of pronuclear(n=220),2-4 cell(n=227)and morula(n=127)were recovered.For each stage,half of the embryos were cultured to the blastocyst and frozen thereafter,while the remainder as control group was frozen just recovery and cultured to the blastocyst;the experimental group of the blastocyst was obtained from uterus and frozen immediately after recovery.The effects on mouse embryos from in vitro culture of early stage to blastocyst stage and on their ability to surviving from cyropreservation were assessed.The survival and birth rate of blastocyst derived from in vitro culture of pronuelear,2-4 cell,morula and blastocyst of in vivo were 56.4%,72.2%,81.6%,95.1% and 38.1%,41.6%,56.8%,74.3%,respectively.The survival and birth rate of pronuclear and 2-4 cell were significantly lower than the control group(P<0.01,P<0.05),which suggests that the viability of early embryos is affected by in vitro culture.The rate of blastocyst derived from in vitro culture of pronuclear and 2-4 cell after thawing is lower than their counterpart(P<0.05):the results indicate that the in vitro culture of pronuclear and 2-4 cell of mouse to the blastocyst stage prior to be frozen improves their survival after thawing.