Abstract
Hair sheep ewes were used to evaluate the influence of various levels of mating stimuli on the duration and timing of estrus and LH concentrations around estrus. Ewes were treated with PGF2α (15 mg, im) 10 d apart. At the time of the second PGF2α treatment (Day 0) ewes were placed in groups and exposed to different types of mating stimuli. One group of ewes (n = 16) was exposed to an epididymectomized ram (RAM), a second group of ewes (n = 16) was exposed to an epididymectomized ram wearing an apron to prevent intromission (APRON) and a third group of ewes (n = 17) was exposed to an androgenized ovariectomized ewe (T-EWE). Jugular blood samples were collected from ewes at 6-h intervals through Day 5. Plasma was harvested and LH concentration was determined by RIA. The ewes were observed at 6-h intervals to detect estrus. A ewe was considered to be out of estrus when she no longer stood to be mounted by the teaser animal. There was no difference (P > 0.10) in the proportion of ewes expressing estrus (79.6%) or having an LH surge (85.7%) among the treatments. Neither the time to estrus nor the duration of estrus were different (P > 0.10) among APRON, RAM or T-EWE groups (41.6 ± 3.8 vs 43.6 ± 3.6 vs 46.1 ± 3.6 h, respectively, and 26.5 ± 2.2 vs 24.8 ± 2.3 vs 30.5 ± 2.2 h, respectively). The time to LH surge was similar (P > 0.10) among APRON, RAM and T-EWE groups (51.2 ± 4.5 vs 51.2 ± 4.7 vs 52.7 ± 4.5 h, respectively). The magntude of the LH surge was similar (P > 0.10) in the T-EWE, APRON and RAM ewes (99.7 ± 4.9 vs 87.2 ± 4.9 vs 85.8 ± 5.0 ng/ml, respectively). The time from estrus to the LH surge was no different (P > 0.10) among APRON, RAM or T-EWE ewes (10.1 ± 2.2 vs 9.8 ± 2.3 vs 11.6 ± 2.3 h, respectively). These results show that the expression and duration of estrus are not influenced by different types of mating stimuli in hair sheep ewes. In addition, the timing and the magnitude of LH release does not appear to be influenced by mating stimuli around the time of estrus.
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