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mRNA transcription of prostaglandin synthases and their products in the equine endometrium in the course of fibrosis

机译:纤维化过程中马内膜中前列腺素合成酶及其产物的mRNA转录

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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-2 alpha 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(2 alpha) 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(2 alpha) 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
机译:生殖周期的精确调节和成功的植入取决于子宫内膜的正常功能。这项研究的目的是确定负责前列腺素(PG)合成的特定酶(前列腺素-过氧化物过氧化物合酶,PTGS-2;前列腺素F-2αPGFS;前列腺素E-2合成酶,PGES)和PG浓度的mRNA转录与健康的子宫内膜(肯尼的I类)相比,在动情周期中,子宫内膜提取物的中度纤维化(肯尼的II类)和严重的纤维化阶段(肯尼的III类;子宫内膜异位)会发生变化。在发情周期的黄体早期(n = 12),中期(n = 12)和晚期(n = 12)以及卵泡期(n = 12)从母马获得子宫内膜组织样品。另外,根据肯尼分类法,所有子宫内膜在显微镜下被分类为属于I类和II类或III类,从而为每个亚类例如黄体中部I,II和III分配4个样品。相对mRNA转录使用实时PCR定量。使用酶联免疫吸附测定(EIA)确定子宫内膜提取物中PGE(2)和PGF(2 alpha)的浓度。在I类中,与黄体早期相比,PTGS-2 mRNA的转录在中黄体期(P <0.05)和黄体后期(P <0.001)和卵泡期(P <0.05)上调。与第一类黄体早期相比,在黄体中期(P <0.01)和后期(P <0.05)PGFS mRNA转录以及PGF(2 alpha)浓度增加。在中期(P与I类的早期黄体和卵泡期相比,<0.01)和黄体后期(P <0.05).I类中的黄体中相(P <0.01)与I期的黄体中和卵泡期相比更高。发情周期。在早期子宫内膜异位期间(II类)和完全子宫内膜异位(III类),与健康子宫内膜中各个发情期相比,PTGS-2,PGFS和PGES mRNA的转录和PG浓度发生了改变(P <0.05)。可以得出结论,在发情周期的纤维化过程中,马内膜中PG合酶mRNA转录和PG产生的mRNA转录的严重变化可能是导致发情周期异常和早期胚胎丢失的障碍的原因。

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