Abstract

Aspiration of bovine follicles 12–36 hours after induced corpus luteum lysis serendipitously identified two populations of cows, one with High androstenedione (A4; >40 ng/ml; mean = 102) and another with Low A4 (<20 ng/ml; mean = 9) in follicular fluid. We hypothesized that the steroid excess in follicular fluid of dominant follicles in High A4 cows would result in reduced fertility through altered follicle development and oocyte maternal RNA abundance. To test this hypothesis, estrous cycles of cows were synchronized and ovariectomy was performed 36 hours later. HPLC MS/MS analysis of follicular fluid showed increased dehydroepiandrosterone (6-fold), A4 (158-fold) and testosterone (31-fold) in the dominant follicle of High A4 cows. However, estrone (3-fold) and estradiol (2-fold) concentrations were only slightly elevated, suggesting a possible inefficiency in androgen to estrogen conversion in High A4 cows. Theca cell mRNA expression of LHCGR, GATA6, CYP11A1, and CYP17A1 was greater in High A4 cows. Furthermore, abundance of ZAR1 was decreased 10-fold in cumulus oocyte complexes from High A4 cows, whereas NLRP5 abundance tended to be 19.8-fold greater (P = 0.07). There was a tendency for reduction in stage 4 follicles in ovarian cortex samples from High A4 cows suggesting that progression to antral stages were impaired. High A4 cows tended (P<0.07) to have a 17% reduction in calving rate compared with Low A4 cows suggesting reduced fertility in the High A4 population. These data suggest that the dominant follicle environment of High A4 cows including reduced estrogen conversion and androgen excess contributes to infertility in part through altered follicular and oocyte development.

Highlights

  • Ovarian steroidogenesis is regulated in a spatial and temporal manner within the granulosa and theca cells of the follicle

  • Cholesterol is transported from the cytosol into the mitochondria by the steroidogenic acute regulatory protein (STAR) [2,3] where it is converted to pregnenolone by cytochrome P450 side-chain cleavage (P450scc or CYP11A1) enzyme

  • As expected we reported increased mRNA abundance of both CYP11A1 and CYP17A1 in High A4 compared with Low A4 theca cells

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Summary

Introduction

Ovarian steroidogenesis is regulated in a spatial and temporal manner within the granulosa and theca cells of the follicle. This regulation is achieved by cell-specific expression of steroidogenic enzymes which regulate conversion of cholesterol to steroid hormones [1]. Cholesterol is transported from the cytosol into the mitochondria by the steroidogenic acute regulatory protein (STAR) [2,3] where it is converted to pregnenolone by cytochrome P450 side-chain cleavage (P450scc or CYP11A1) enzyme. The third carbon of DHEA is subsequently dehydrogenated by 3b-hydroxysteroid dehydrogenase (HSD3B) to form androstenedione (A4) [1]. A4 can first be converted to testosterone (T) by HSD17B and hydroxylated via CYP19A1 to form E2 [1]

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