Abstract

Reproductive performance in seasonally anestrous ewes is poor even after the use of current controlled breeding protocols. Anestrous ewes treated with a medroxyprogesterone acetate sponge, for 12 or 14 d, and estradiol-17β (E2) have synchronized follicular wave emergence. The objective of this study was to determine the effects of an E2 injection 6 d after CIDR insertion on follicles, E2 and LH concentrations, and estrus in seasonally anestrous ewes. Ewes (n = 13) received CIDRs (Day -12) followed by an injection of eCG (500 IU; i.m.; Day 0) at CIDR removal and an injection of sesame oil without (1 mL; i.m.; Control) or with E2 (350µg; i.m.; Day -6) 6 d before CIDR removal. Treatments were balanced for age, parity, and BCS. Blood samples were collected every 6 h for 48 h after E2 injection and every 3 h for 60 h starting 18 h after eCG injection to determine LH concentrations. Blood samples were collected on Day -6 and 0 and every 6 h for 60 h starting 18 h after eCG injection to determine E2 concentrations. Ovarian ultrasonography was done on Day -6 and 0. A ram was introduced on Day 1 to observe estrus. Ewes treated with E2 had higher LH concentrations (0.37 ± 0.05 ng/mL) than ewes treated with oil alone (0.12±0.05 ng/mL) during the 48 h after E2 injection (P < 0.005). Concentrations of LH were highest at 18 h after E2 injection (1.11 ± 0.12 ng/mL; P < 0.001). Ewes treated with E2 had higher LH concentrations (2.10 ± 0.18 ng/mL) than ewes treated with oil alone (0.12 ± 0.16 ng/mL) at 18 h after E2 injection (P < 0.001). The interval from eCG injection to the start of the pre-ovulatory LH surge was similar (37.1 ± 4.4 h; P > 0.05), but was more synchronized in ewes treated with E2 (2.3 ± 0.6 h) than ewes treated with oil alone (12.0 ± 5.1 h; P < 0.01). Concentrations of E2 were similar between treatments on Day -6 (2.1 ± 0.3 pg/mL; P > 0.05) and Day 0 (2.3 ± 0.4 pg/mL; P > 0.05). Concentrations of E2 tended to be highest at 18 h after eCG injection (3.5 ± 0.5 pg/mL; P = 0.076). Maximum follicular diameter was larger on Day 0 (4.8 ± 0.2 mm) than Day -6 (3.4 ± 0.2 mm; P < 0.001). There were no differences in the interval from eCG treatment to the start (37.6 ± 2.7 h) or end (74.7 ± 1.9 h) of estrus (P > 0.05). Adding an E2 treatment during a CIDR-eCG estrus synchronization protocol increased LH concentrations after E2 treatment and stimulated a more synchronized pre-ovulatory LH surge in seasonally anestrous ewes.

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