Intrauterine infusion of BQ-610, an endothelin type A receptor antagonist, delays luteolysis in dairy heifers

Three separate in vivo experiments were conducted to evaluate the putative role of endothelin-1 (ET-1) during luteal regression in heifers. In Experiment 1, a single intraluteal injection of 500μg BQ-610 [(N,N-hexamethylene) carbamoyl-Leu-d-Trp (CHO)-d-Trp], a highly specific endothelin A (ETA) rece...

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Veröffentlicht in:Domestic animal endocrinology 2008-05, Vol.34 (4), p.411-418
Hauptverfasser: Keator, Christopher S., Schreiber, David T., Hoagland, Thomas A., McCracken, John A., Milvae, Robert A.
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Sprache:eng
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Zusammenfassung:Three separate in vivo experiments were conducted to evaluate the putative role of endothelin-1 (ET-1) during luteal regression in heifers. In Experiment 1, a single intraluteal injection of 500μg BQ-610 [(N,N-hexamethylene) carbamoyl-Leu-d-Trp (CHO)-d-Trp], a highly specific endothelin A (ETA) receptor antagonist, did not diminish the decline in plasma progesterone following a single exogenous injection of 25mg prostaglandin F2 alpha (PGF2α) administered at midcycle of the estrous cycle. In Experiment 2, six intrauterine infusions of 500μg BQ-610 given every 12h on days 16–18 delayed spontaneous luteolysis, as evidenced by an extended elevation (P=0.054) of plasma progesterone concentration. In Experiment 3, heifers were administered six intrauterine infusions of BQ-610 or saline on days 16–19, and peripheral blood samples were collected from day 11 to 16 (before infusion), hourly on days 16–19 (during infusion), and on days 20–25 (after infusion). BQ-610 treated heifers had markedly higher (P
ISSN:0739-7240
1879-0054
DOI:10.1016/j.domaniend.2007.11.002