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Volume 74, Issue 3, Pages 384-392 (August 2010)


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Stimulation of pulses of 13,14-dihydro-15-keto-PGF2α (PGFM) with estradiol-17β and changes in circulating progesterone concentrations within a PGFM pulse in heifers

O.J. GintherabCorresponding Author Informationemail address, H.K. Shresthaa, M.J. Fuenzalidaa, S. Imama, M.A. Begb

Received 19 January 2010; received in revised form 19 February 2010; accepted 24 February 2010. published online 23 April 2010.

Abstract 

A single physiologic dose (0.1 mg) of estradiol-17β in sesame-oil vehicle or vehicle alone (n = 8) was given to heifers on day 14 after ovulation to study the effect on circulating 13-14-dihydro-15-keto-PGF2α (PGFM), PGFM pulses, and changes in progesterone concentrations within a PGFM pulse. Blood samples were collected hourly for 16 h after treatment. The estradiol group had a greater mean concentration of PGFM, greater number of heifers with PGFM pulses and number of pulses/heifer, and greater prominence of the PGFM pulses. Changes in progesterone concentrations were not detected during the 16 h sampling session in the vehicle group, indicating that the heifers were in preluteolysis. Progesterone decreased after 12 h in the estradiol group, indicating a luteolytic effect of the estradiol-induced PGF secretion as represented by PGFM concentrations. Intrapulse changes in progesterone were detected during a PGFM pulse in the estradiol group (P < 0.006), but not in the vehicle group. Progesterone increased (P < 0.01) between Hours −2 and −1 of an estradiol-induced PGFM pulse (Hour 0 = peak of pulse), decreased (P < 0.004) between Hours −1 and 0, and increased (P < 0.01) or rebounded between Hours 0 and 1. Results were compatible with previous reports of a role for estradiol in the induction of PGFM pulses in cattle and demonstrated intrapulse changes in progesterone concentrations during an induced PGFM pulse.

a Eutheria Foundation, Cross Plains, Wisconsin 53528, USA

b Department of Pathobiological Sciences, University of Wisconsin, Madison, Wisconsin 53706, USA

Corresponding Author InformationCorresponding author. Tel.: +1 608 798 3777; fax: +1 608 798 4910

PII: S0093-691X(10)00136-6

doi:10.1016/j.theriogenology.2010.02.021


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