role of thecal androgen production in the regulation of estradiol biosynthesis by dominant bovine follicles during the first follicular wave

• Published in: Journal of animal science 2005-03, Vol.83 (3), p.597-603
• Main Authors: Valdez, K. E, Cuneo, S. P, Gorden, P. J, Turzillo, A. M
• Format: Article
• Language: English
• Subjects: 17alpha-hydroxylase; androstenedione; Androstenedione - secretion; Animal productions; Animals; aromatase; biochemical mechanisms; Biological and medical sciences; biosynthesis; Cattle - physiology; cows; enzyme activity; estradiol; Estradiol - analysis; Estradiol - biosynthesis; Estradiol - genetics; Estradiol - secretion; Female; follicular atresia; Follicular Fluid - chemistry; Fundamental and applied biological sciences. Psychology; gene expression; gene expression regulation; Gene Expression Regulation - physiology; granulosa cells; Granulosa Cells - chemistry; Granulosa Cells - physiology; Granulosa Cells - secretion; heifers; Holstein; hormonal regulation; hormone secretion; messenger RNA; Ovarian Follicle - chemistry; Ovarian Follicle - physiology; ovulation; oxygenases; Reproduction - physiology; RNA, Messenger - metabolism; Terrestrial animal productions; Theca Cells - physiology; Theca Cells - secretion; thecal cells; Time Factors; Vertebrates
• ISSN: 0021-8812; 1525-3163
• DOI: 10.2527/2005.833597x

The first wave of follicular development following ovulation in cattle is characterized by selection and growth of a large, estrogenic dominant follicle. After the follicle becomes morphologically dominant, concentrations of estradiol in its follicular fluid decrease abruptly. The purpose of this study was to determine whether this decrease in estrogen production is caused by an insufficient supply of androgen from theca interna or decreased aromatization of androgen precursor by granulosa cells. Dominant follicles were collected from Holstein heifers on d 4, 6, or 8 of the first follicular wave (n = 5/d). Amounts of 17[alpha]-hydroxylase mRNA in theca interna were sevenfold higher (P < 0.01) on d 4 than on d 8. After 3 h in culture, secretion of androstenedione by theca interna collected on d 4 (236 ± 44 pg/[micro]g of protein) tended to be lower (P = 0.055) compared with d 6 (517 ± 162 pg/[micro]g protein) and was lower (P < 0.05) compared with d 8 (387 ± 51 pg/[micro]g of protein). In granulosa cells, amounts of aromatase mRNA decreased (P < 0.05) on d 8 compared with d 6 but not d 4. In vitro secretion of estradiol was higher in granulosa cells collected on d 4 (3.5 ± 0.8 ng/[10⁵ cells x 3 h]) compared with d 6 (1.8 ± 0.6 ng/[10⁵ cells x 3 h]; P < 0.05) and tended to be higher on d 4 than on d 8 (2.2 ± 0.2 ng/[10⁵ cells x 3 h]; P = 0.058). We conclude that the decrease in estradiol production observed during atresia of the dominant follicle is not due to lack of androgen substrate for aromatization or downregulated expression of the aromatase gene, but may be the direct result of decreased activity of the aromatase enzyme within granulosa cells.