Dovolou E, Messinis I E, Periquesta E, Dafopoulos K, Gutierrez-Adan A, Amiridis G S
Department of Obstetrics & Reproduction, Veterinary Faculty, University of Thessaly, Karditsa, Greece.
Department of Obstetrics & Gynecology, Faculty of Medicine, University of Thessaly, Larissa, Greece.
Reprod Domest Anim. 2014 Aug;49(4):665-672. doi: 10.1111/rda.12344. Epub 2014 Jun 2.
Ghrelin, apart from its metabolic role, is nowadays considered as a basic regulator of reproductive functions of mammals, acting at central and gonadal levels. Here, we investigated for possible direct actions of ghrelin on in vitro maturation of bovine oocytes and for its effects on blastocyst yield and quality. In experiment 1, cumulus oocyte complexes (COCs) were matured in the presence of four different concentrations of ghrelin (0, 200, 800 and 2000 pg/ml). In vitro fertilization and embryo culture were carried out in the absence of ghrelin, and blastocyst formation rates were examined on days 7, 8 and 9. In experiment 2, only the 800 pg/ml dose of ghrelin was used. Four groups of COCs were matured for 18 or 24 h (C18, Ghr18, C24 and Ghr24), and subsequently, they were examined for oocyte nuclear maturation and cumulus layer expansion; blastocysts were produced as in experiment 1. The relative mRNA abundance of various genes related to metabolism, oxidation, developmental competence and apoptosis was examined in snap-frozen cumulus cells, oocytes and day-7 blastocysts. In experiment 1, ghrelin significantly suppressed blastocyst formation rates. In experiment 2, more ghrelin-treated oocytes matured for 18 h reached MII compared with controls, while no difference was observed when maturation lasted for 24 h. At 18 and 24 h, the cumulus layer was more expanded in ghrelin-treated COCs than in the controls. The blastocyst formation rate was higher in Ghr18 (27.7 ± 2.4%) compared with Ghr24 (17.5 ± 2.4%). Differences were detected in various genes' expression, indicating that in the presence of ghrelin, incubation of COCs for 24 h caused over-maturation (induced ageing) of oocytes, but formed blastocysts had a higher hatching rate compared with the controls. We infer that ghrelin exerts a specific and direct role on the oocyte, accelerating its maturational process.
胃饥饿素除了具有代谢作用外,如今还被认为是哺乳动物生殖功能的一种基本调节因子,在中枢和性腺水平发挥作用。在此,我们研究了胃饥饿素对牛卵母细胞体外成熟的可能直接作用及其对囊胚产量和质量的影响。在实验1中,卵丘卵母细胞复合体(COCs)在四种不同浓度的胃饥饿素(0、200、800和2000 pg/ml)存在的情况下进行成熟培养。体外受精和胚胎培养在无胃饥饿素的条件下进行,并在第7、8和9天检查囊胚形成率。在实验2中,仅使用800 pg/ml剂量的胃饥饿素。四组COCs分别成熟培养18或24小时(C18、Ghr18、C24和Ghr24),随后检查卵母细胞核成熟情况和卵丘层扩张情况;如实验1那样产生囊胚。在速冻的卵丘细胞、卵母细胞和第7天的囊胚中检测了与代谢、氧化、发育能力和凋亡相关的各种基因的相对mRNA丰度。在实验1中,胃饥饿素显著抑制了囊胚形成率。在实验2中,与对照组相比,经胃饥饿素处理18小时成熟的卵母细胞中有更多达到了第二次减数分裂中期(MII),而当成熟培养持续24小时时未观察到差异。在18小时和24小时时,经胃饥饿素处理的COCs的卵丘层比对照组的更扩张。与Ghr24组(17.5±2.4%)相比,Ghr18组的囊胚形成率更高(27.7±2.4%)。在各种基因的表达中检测到差异,表明在胃饥饿素存在的情况下,COCs培养24小时会导致卵母细胞过度成熟(诱导老化),但形成的囊胚与对照组相比具有更高的孵化率。我们推断胃饥饿素对卵母细胞发挥着特定的直接作用,加速其成熟过程。