Abstract

The aim of this study was to characterize the regulation pattern of prostaglandin family members namely prostaglandin F2alpha (PTGF), prostaglandin E2 (PTGE), their receptors (PTGFR, PTGER2, PTGER4), cyclooxygenase 2 (COX-2), PTGF synthase (PTGFS), and PTGE synthase (PTGES) in the bovine follicles during preovulatory period and early corpus luteum (CL). Ovaries containing preovulatory follicles or CL were collected by transvaginal ovariectomy (n = 5 cows/group), and the follicles were classified: (I) before GnRH treatment; (II) 4 h after GnRH; (III) 10 h after GnRH; (IV) 20 h after GnRH; (V) 25 h after GnRH, and (VI) 60 h after GnRH (early CL). In these samples, the concentrations of progesterone (P4), estradiol (E2), PTGF and PTGE were investigated in the follicular fluid (FF) by validated EIA. Relative mRNA abundance of genes encoding for prostaglandin receptors (PTGFR, PTGER2, PTGER4), COX-2, PTGFS and PTGES were quantified by RT-qPCR. The localization of COX-2 and PTGES were investigated by established immunohistochemistry in fixed follicular and CL tissue samples. The high E2 concentration in the FF of the follicle group before GnRH treatment (495.8 ng/ml) and during luteinizing hormone (LH) surge (4 h after GnRH, 574.36 ng/ml), is followed by a significant (P<0.05) downregulation afterwards with the lowest level during ovulation (25 h after GnRH, 53.11 ng/ml). In contrast the concentration of P4 was very low before LH surge (50.64 mg/ml) followed by a significant upregulation (P < 0.05) during ovulation (537.18 ng/ml). The mRNA expression of COX-2 increased significantely (P < 0.05) 4 h after GnRH and again 20 h after GnRH, followed by a significant decrease (P < 0.05) after ovulation (early CL). The mRNA of PTGFS in follicles before GnRH was high followed by a continuous and significant downregulation (P < 0.05) afterwards. In contrast, PTGES mRNA abundance increased significantely (P < 0.05) in follicles 20 h after GnRH treatment and remained high afterwards. The mRNA abundance of PTGFR, PTGER2, and PTGER4 in follicles before GnRH was high, followed by a continuous and significant down regulation afterwards and significant increase (P < 0.05) only after ovulation (early CL). The low concentration of PTGF (0.04 ng/ml) and PTGE (0.15 ng/ml) in FF before GnRH, increased continuously in follicle groups before ovulation and displayed a further significant and dramatic increase (P < 0.05) around ovulation (101.01 ng/ml, respectively, 484.21 ng/ml). Immunohistochemically, the granulosa cells showed an intensive signal for COX-2 and PTGES in follicles during preovulation and in granulosa-luteal cells of the early CL. In conclusion, our results indicate that the examined bovine prostaglandin family members are involved in the local mechanisms regulating final follicle maturation and ovulation during the folliculo-luteal transition and CL formation.

Highlights

  • The ovarian cycle in bovine is characterized by regularly repeating patterns of cellular proliferation, differentiation and transformation that accompanies follicular maturation and ovulation during the folliculo-luteal transition and corpus lutem (CL) formation and function [1,2,3,4,5]

  • Recent studies have demonstrated the important role of steroid hormones and prostaglandins during follicle development, ovulation and CL formation in different species and various study models [8, 22, 31, 47, 48]

  • Our present study demonstrates the expression pattern of steroid hormones (E2 and P4) and prostaglandin family members (COX-2, prostaglandin F2alpha (PTGF) synthase (PTGFS), prostaglandin E2 (PTGE) synthase (PTGES), PTGF, PTGE, and their receptors) in different timely defined follicle classes before and after GnRH application and after ovulation in the cow

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Summary

Introduction

The ovarian cycle in bovine is characterized by regularly repeating patterns of cellular proliferation, differentiation and transformation that accompanies follicular maturation and ovulation during the folliculo-luteal transition and corpus lutem (CL) formation and function [1,2,3,4,5]. Ovulation occurs as a result of a dynamic interaction between the luteinising hormone (LH) surge and local follicular factors including steroid hormones, extracellular matrix (ECM) proteases, prostaglandins, vasoactive peptides and growth factors in a time-dependent manner [1, 13,14,15]. During these developments in the bovine ovary, steroid hormones and prostaglandins seem to be highly important regulatory mediators playing a central role in the regulation of the estrous cycle [16,17,18,19,20,21,22]. The later stage of follicular development, ovulation and CL formation depends upon growth of new blood vessels (angiogenesis) and the establishment of a functional blood supply [12, 26, 27]

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