Department of Reproductive Immunology and Pathology, Institute of Animal Reproduction and Food Research, Olsztyn, Poland.
Theriogenology. 2012 Sep 1;78(4):768-76. doi: 10.1016/j.theriogenology.2012.03.024. Epub 2012 May 11.
Accurate regulation of the reproductive cycle and successful implantation depend on proper functioning of the endometrium. The aim of this study was to determine whether mRNA transcription of specific enzymes responsible for prostaglandin (PG) synthesis (prostaglandin-endoperoxide synthase, PTGS-2; prostaglandin F(2α) synthase, PGFS; and prostaglandin E(2) synthases, PGES) and PG concentrations in endometrial extracts would change in moderate (Kenney's Category II) and severe phases of fibrosis (Kenney's Category III; endometrosis), compared with healthy endometrium (Kenney's Category I), during the estrous cycle. Endometrial tissues samples were obtained from mares at the early (n = 12), mid (n = 12) and late (n = 12) luteal phases and the follicular phase (n = 12) of the estrous cycle. Additionally, all endometria were classified microscopically as belonging to Categories I and II or III according to the Kenney classification, resulting in allocation of 4 samples for each subcategory, e.g., mid luteal I, II and III. Relative mRNA transcription was quantified using Real-time PCR. Concentrations of PGE(2) and PGF(2α) in the endometrial extracts were determined using enzyme-linked immunosorbent assay (EIA). In Category I, PTGS-2 mRNA transcription was upregulated at the mid (P < 0.05) and late luteal phases (P < 0.001) and at the follicular phase (P < 0.05) compared to the early luteal phase. PGFS mRNA transcription as well as PGF(2α) concentrations increased at the mid (P < 0.01) and late (P < 0.05) luteal phases compared to the early luteal phase in Category I. PGES mRNA transcription was higher at the mid (P < 0.01) and late luteal phases (P < 0.05) compared to the early luteal and follicular phases in Category I. Prostaglandin E(2) concentration in Category I was higher at the mid luteal phase (P < 0.01) compared to all other phases of the estrous cycle. During incipient endometrosis (Category II) and under full endometrosis (Category III), PTGS-2, PGFS and PGES mRNA transcription and PG concentration were altered compared to the respective estrous phases in healthy endometria (P < 0.05). It may be concluded that serious changes in mRNA transcription of PG synthases and PG production that occur in the equine endometrium during the course of fibrosis in the estrous cycle could be responsible for disturbances leading to disorders of the estrous cycle and early embryo losses.
准确的生殖周期调节和成功的着床依赖于子宫内膜的正常功能。本研究的目的是确定在发情周期中,与健康的子宫内膜(Kenney 分类 I)相比,中度(Kenney 分类 II)和重度(Kenney 分类 III;子宫内膜异位症)纤维化阶段(Kenney 分类 II)的特定负责前列腺素(PG)合成的酶(前列腺素内过氧化物合酶,PTGS-2;前列腺素 F(2α)合酶,PGFS;和前列腺素 E(2)合酶,PGES)的 mRNA 转录和 PG 浓度是否会发生变化。在发情周期中,从发情周期的早期(n = 12)、中期(n = 12)和晚期(n = 12)黄体期以及卵泡期(n = 12)获得马的子宫内膜组织样本。此外,所有子宫内膜均根据 Kenney 分类法显微镜分类为 I 类和 II 类或 III 类,这导致每个亚类分配 4 个样本,例如,中期黄体 I、II 和 III。使用实时 PCR 定量相对 mRNA 转录。使用酶联免疫吸附测定(EIA)测定子宫内膜提取物中 PGE(2)和 PGF(2α)的浓度。在 I 类中,PTGS-2 mRNA 转录在中期(P < 0.05)和晚期黄体期(P < 0.001)以及卵泡期(P < 0.05)与早期黄体期相比上调。PGFS mRNA 转录以及 PGF(2α)浓度在 I 类中在中期(P < 0.01)和晚期(P < 0.05)黄体期与早期黄体期相比升高。PGES mRNA 转录在 I 类中在中期(P < 0.01)和晚期黄体期(P < 0.05)与早期黄体期和卵泡期相比升高。PGES 在 I 类中,与发情周期的其他阶段相比,中期黄体期(P < 0.01)的前列腺素 E(2)浓度更高。在初期子宫内膜异位症(II 类)和完全子宫内膜异位症(III 类)中,与健康子宫内膜的发情期相比,PG 合酶和 PG 产生的 mRNA 转录和 PG 浓度发生改变(P < 0.05)。可以得出结论,在发情周期中纤维化过程中马子宫内膜中 PG 合酶的 mRNA 转录和 PG 产生的严重变化可能导致导致发情周期紊乱和早期胚胎丢失的紊乱。