Paragon Veterinary Group, Carlisle House, Townhead Rd, Dalston, Cumbria, CA7 7JF, UK; School of Biosciences, University of Nottingham, Sutton Bonington Campus, Leicestershire, LE12 5RD, UK.
School of Biosciences, University of Nottingham, Sutton Bonington Campus, Leicestershire, LE12 5RD, UK.
Theriogenology. 2023 Mar 15;199:77-85. doi: 10.1016/j.theriogenology.2023.01.003. Epub 2023 Jan 4.
The in vitro production (IVP) of cattle embryos requires that germinal-vesicle stage oocytes undergo a period of maturation in vitro prior to fertilization and culture to the blastocyst stage. Success of IVP in taurine cattle is enhanced following ovarian stimulation prior to oocyte retrieval (OPU), particularly if preceded by a short period of FSH withdrawal ('coasting'). However, evidence regarding the importance of progesterone (P4) support during OPU-IVP is equivocal. The current study, therefore, determined the effects of increased peripheral P4 concentrations during FSH-stimulated ('coasted') cycles of OPU. Progesterone support was provided by either an active corpus luteum (CL) and/or one of two intravaginal P4 releasing devices (i.e., CIDR® [1.38 g P4] or PRID® Delta [1.55 g P4]). Expt. 1 established an initial estrus prior to OPU, allowing CL formation (single luteal phase) spanning the first two of five cycles of OPU; the remaining three cycles were supported by either a CIDR® or PRID® Delta. Expt. 2 commenced with two cycles of dominant follicle removal (including prostaglandin F) undertaken seven days apart prior to six cycles of OPU. The absence of a CL meant that these cycles were supported only by a CIDR® or PRID® Delta. As each experiment involved several sequential cycles of OPU, the cumulative effects of device use on vaginal discharges were also assessed. Each experiment involved 10 sexually mature Holstein heifers. In the absence of a CL, peak plasma P4 concentrations were greater (P = 0.002) for the PRID® Delta (4.3 ± 0.22) than for the CIDR® (2.9 ± 0.22). In Expt. 1 there was an interaction (P < 0.05) between CL presence at OPU and P4 device on Day 8 blastocyst yields, indicating an effect of P4 device only when the CL was absent. The percentage hatching/hatched blastocysts of matured oocytes for the CIDR® and PRID® Delta was 44.3 ± 5.04 and 41.0 ± 5.40 in the presence, and 17.1 ± 3.48 and 42.2 ± 3.76 in the absence, of a CL (P = 0.018). Combined analyses of data from Expt. 1 and 2, when no CL was present, confirmed that Day 8 blastocyst yields were greater (P = 0.022) for the PRID® Delta than the CIDR®. Vaginal discharge scores were higher (P < 0.001) for the PRID® Delta than the CIDR® in Expt. 1 but not in Expt 2; however scores were low, did not increase with repeated use, and thus were deemed of no clinical or welfare concern. In conclusion, enhanced P4 support during FSH-stimulated cycles of OPU-IVP can improve in vitro embryo development.
牛胚胎的体外生产(IVP)要求卵母细胞在受精和培养到囊胚阶段之前,在体外经历一个成熟阶段。在卵巢刺激后进行卵母细胞采集(OPU)前,牛的 IVP 成功率得到提高,特别是如果在此之前进行短暂的 FSH 停药(“滑行”)。然而,关于 OPU-IVP 期间孕酮(P4)支持的重要性的证据尚无定论。因此,本研究旨在确定在 FSH 刺激的(“滑行”)OPU 周期中增加外周 P4 浓度的影响。孕酮支持通过活性黄体(CL)和/或两种阴道内 P4 释放装置(即 CIDR®[1.38 g P4]或 PRID®Delta[1.55 g P4])提供。实验 1 在 OPU 前建立了一个初始发情期,允许 CL 形成(单一黄体期)跨越 OPU 的前两个五个周期中的两个;剩余的三个周期由 CIDR®或 PRID®Delta 支持。实验 2 从两个单独的优势卵泡去除(包括前列腺素 F)周期开始,间隔七天,然后进行六个 OPU 周期。由于没有 CL,这些周期仅由 CIDR®或 PRID®Delta 支持。由于每个实验都涉及多个连续的 OPU 周期,因此还评估了设备使用对阴道分泌物的累积影响。每个实验都涉及 10 头性成熟的荷斯坦奶牛。在没有 CL 的情况下,PRID®Delta(4.3±0.22)的峰值血浆 P4 浓度高于 CIDR®(2.9±0.22)(P=0.002)。在实验 1 中,在 OPU 时 CL 的存在和 P4 装置之间存在相互作用(P<0.05),这表明仅在没有 CL 时才存在 P4 装置的影响。CIDR®和 PRID®Delta 成熟卵母细胞的孵化/孵化囊胚百分比为 44.3±5.04 和 41.0±5.40,CL 存在时为 17.1±3.48 和 42.2±3.76(CL 不存在时)(P=0.018)。实验 1 和 2 的数据分析综合分析,当不存在 CL 时,PRID®Delta 的第 8 天囊胚产量高于 CIDR®(P=0.022)。在实验 1 中,PRID®Delta 的阴道分泌物评分高于 CIDR®(P<0.001),但在实验 2 中则不然;然而,评分较低,随着重复使用而没有增加,因此被认为没有临床或福利问题。总之,在 FSH 刺激的 OPU-IVP 周期中增加 P4 支持可以提高体外胚胎发育。