Hill J, Gilbert R
Department of Clinical Sciences, College of Veterinary Medicine, Cornell University, New York 14853-6401, USA.
Aust Vet J. 2008 Aug;86(8):312-6. doi: 10.1111/j.1751-0813.2008.00326.x.
A suboptimal uterine environment contributes to the bovine repeat breeder syndrome. Subclinical endometritis is a component, so the mechanism by which inflammation affects embryo survival was investigated by assessing the effect of non-cellular products of an inflamed endometrium on embryo development to blastocyst.
Endometrial fluid from a lactating dairy cow was collected by lavage using embryo culture medium. Aseptic inflammation was then induced by infusion of glycogen and lavage was repeated 6 h later. The recovered fluid was used to culture Day 5 in-vitro-derived embryos for 2 days. Embryo development and quality were compared for two treatment groups (culture media conditioned by inflamed or non-inflamed endometrium) and two controls (control or control + serum).
Development to blastocyst was higher for conditioned media or media + serum (inflamed 42.2%; non-inflamed 49.3%; control + serum 50.9%; control 16.9%; P < 0.001). Blastocyst cell numbers were lower for the conditioned-inflamed group (inflamed, 83.1; non-inflamed, 99.8; control + serum, 100.6; control, 110.1; P < 0.001). Trophectoderm cell number, but not inner cell mass number, was reduced in the conditioned-inflamed group and the inner cell mass:trophectoderm ratio was increased (P < 0.001).
Altering the embryo culture environment with the products of endometrial inflammation had a subtle effect on embryo quality. An increased inner cell mass:trophoblast ratio is likely to negatively affect embryonic survival. Altered embryo quality is a mechanism for early embryonic failure in cows with subclinical endometritis. Culture of embryos with normal endometrial fluid may improve in vitro embryo production.
子宫环境欠佳会导致奶牛屡配不孕综合征。亚临床子宫内膜炎是其中一个因素,因此通过评估炎症子宫内膜的无细胞产物对胚胎发育至囊胚的影响,来研究炎症影响胚胎存活的机制。
使用胚胎培养基通过灌洗收集泌乳奶牛的子宫内膜液。然后通过注入糖原诱导无菌性炎症,并在6小时后重复灌洗。回收的液体用于将第5天的体外衍生胚胎培养2天。比较两个处理组(由炎症或非炎症子宫内膜调节的培养基)和两个对照组(对照或对照+血清)的胚胎发育和质量。
调节培养基或培养基+血清的囊胚发育率更高(炎症组42.2%;非炎症组49.3%;对照+血清组50.9%;对照组16.9%;P<0.001)。炎症调节组的囊胚细胞数量较低(炎症组83.1;非炎症组99.8;对照+血清组100.6;对照组110.1;P<0.001)。炎症调节组的滋养外胚层细胞数量减少,但内细胞团数量未减少,内细胞团:滋养外胚层比例增加(P<0.001)。
用子宫内膜炎症产物改变胚胎培养环境对胚胎质量有微妙影响。内细胞团:滋养层比例增加可能会对胚胎存活产生负面影响。胚胎质量改变是亚临床子宫内膜炎奶牛早期胚胎失败的一种机制。用正常子宫内膜液培养胚胎可能会提高体外胚胎生产效率。