Moore S G, Scully S, Browne J A, Fair T, Butler S T
Animal and Grassland Research and Innovation Centre, Teagasc, Moorepark, Fermoy, Co. Cork, Ireland; School of Agriculture and Food Science, University College Dublin, Belfield, Dublin 4, Ireland.
School of Agriculture and Food Science, University College Dublin, Belfield, Dublin 4, Ireland.
J Dairy Sci. 2014 Sep;97(9):5543-57. doi: 10.3168/jds.2014-8133. Epub 2014 Jun 18.
This study investigated the factors affecting circulating progesterone (P4) concentrations in cows with similar genetic merit for milk production traits, but with extremes of good (Fert+) or poor (Fert-) genetic merit for fertility traits. Study 1: 28 cows were enrolled in an ovulation synchronization protocol at 61±13 (±standard deviation) days postpartum, and data are presented for 13 Fert+ and 9 Fert- cows that remained in the study. Progesterone concentrations were determined from d 0 to 9 (d 0=estrus) and on d 7, corpus luteum (CL) volume and blood flow area (BFA) were measured by B-mode and Doppler ultrasonography, respectively. Cows were administered PGF2α on d 7 in the p.m. and d 8 in the a.m. to regress the CL, and 2 controlled internal drug release devices were inserted per vaginum on d 8 in the a.m. Liver biopsies were collected on d 9 and hepatic mRNA abundance of genes involved in P4 catabolism was determined. On d 10, the controlled internal drug release inserts were removed and frequent blood samples were collected to measure the rate of decline in circulating P4. The Fert+ cows tended to have greater dry matter intake compared with Fert- cows (+0.79kg of dry matter/d), but similar milk production (29.82kg/d). After synchronized ovulation, the rate of increase in circulating P4 concentrations was greater in Fert+ cows compared with Fert- cows. No effect of genotype on CL volume was detected, but BFA was 42% greater in Fert+ cows compared with Fert- cows. The Fert- cows had greater mRNA abundance of cytochrome P450, family 3, subfamily A (CYP3A) compared with Fert+ cows, but the mRNA abundance of aldo-keto reductase family 1, member C1 (AKR1C1), AKR1C3, AKR1C4, and cytochrome P450, family 2, subfamily C (CYP2C) were similar. The half-life and metabolic clearance rate of P4 were similar in Fert+ cows and Fert- cows. Study 2: 23 cows were enrolled in an ovulation synchronization protocol at 55±7 (±standard deviation) d postpartum, and data are presented for 13 Fert+ and 8 Fert- cows that remained in the study. On d 4, 7, 10, and 13 (d 0=estrus), CL volume and BFA were measured as in study 1. Progesterone concentrations were measured from d 1 to 13. Corpus luteum volume was 41% greater in Fert+ cows compared with Fert- cows but no effect of genotype on BFA was detected. Mean circulating P4 concentrations were 79% greater in Fert+ cows compared with Fert- cows. Milk yield was similar in both genotypes. The results indicate that greater circulating P4 concentrations were primarily due to greater CL P4 synthetic capacity rather than differences in P4 clearance in this lactating cow genetic model of fertility.
本研究调查了影响产奶性状遗传 merit 相似,但繁殖性状遗传 merit 分别为优良(Fert+)或不良(Fert-)的奶牛循环孕酮(P4)浓度的因素。研究 1:28 头奶牛在产后 61±13(±标准差)天参加排卵同步方案,本研究报告了 13 头 Fert+奶牛和 9 头 Fert-奶牛的数据。从第 0 天至第 9 天(第 0 天=发情期)测定孕酮浓度,并在第 7 天分别通过 B 型和多普勒超声测量黄体(CL)体积和血流面积(BFA)。在下午第 7 天和上午第 8 天给奶牛注射 PGF2α以消退 CL,并在上午第 8 天每个阴道插入 2 个控制内部药物释放装置。在第 9 天采集肝脏活检样本并测定参与 P4 分解代谢的基因的肝脏 mRNA 丰度。在第 10 天,取出控制内部药物释放插入物并采集频繁的血样以测量循环 P4 的下降速率。与 Fert-奶牛相比,Fert+奶牛的干物质摄入量往往更高(多 0.79 千克干物质/天),但产奶量相似(29.82 千克/天)。排卵同步后,与 Fert-奶牛相比,Fert+奶牛循环 P4 浓度的增加速率更大。未检测到基因型对 CL 体积的影响,但与 Fert-奶牛相比,Fert+奶牛的 BFA 大 42%。与 Fert+奶牛相比,Fert-奶牛细胞色素 P450 家族 3 亚家族 A(CYP3A)的 mRNA 丰度更高,但醛酮还原酶家族 1 成员 C1(AKR1C1)、AKR1C3、AKR1C4 和细胞色素 P450 家族 2 亚家族 C(CYP2C)的 mRNA 丰度相似。Fert+奶牛和 Fert-奶牛中 P4 的半衰期和代谢清除率相似。研究 2:23 头奶牛在产后 55±7(±标准差)天参加排卵同步方案,本研究报告了 13 头 Fert+奶牛和 8 头 Fert-奶牛的数据。在第 4、7、10 和 13 天(第 0 天=发情期),如研究 1 中那样测量 CL 体积和 BFA。从第 1 天至第 13 天测量孕酮浓度。与 Fert-奶牛相比,Fert+奶牛的黄体体积大 41%,但未检测到基因型对 BFA 的影响。与 Fert-奶牛相比,Fert+奶牛的平均循环 P4 浓度高 79%。两种基因型的产奶量相似。结果表明,在这种泌乳奶牛繁殖力遗传模型中,循环 P4 浓度更高主要是由于 CL 的 P4 合成能力更强,而非 P4 清除存在差异。