Lutalyse® induces uterine-ovarian PGF₂α release in sheep: a critical component of induced luteolysis

Exogenous PGF<sub>2α</sub>, (see Appendix I for definitions of abbreviations) is luteolytic in midluteal (1.e., d 9 of a 17 d estrous cycle) sheep. However, the pharmacokinetic responses to PGF<sub>2α</sub>-induced luteolysis are not known. This study (Exp. 1 and 2) was condu...

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Main Author: Wade, Dawn E.
Other Authors: Animal and Poultry Sciences
Format: Others
Language:en
Published: Virginia Tech 2014
Subjects:
Online Access:http://hdl.handle.net/10919/43803
http://scholar.lib.vt.edu/theses/available/etd-07212009-040504/
id ndltd-VTETD-oai-vtechworks.lib.vt.edu-10919-43803
record_format oai_dc
collection NDLTD
language en
format Others
sources NDLTD
topic LD5655.V855 1994.W334
Luteinizing hormone
Sheep -- Physiology
spellingShingle LD5655.V855 1994.W334
Luteinizing hormone
Sheep -- Physiology
Wade, Dawn E.
Lutalyse® induces uterine-ovarian PGF₂α release in sheep: a critical component of induced luteolysis
description Exogenous PGF<sub>2α</sub>, (see Appendix I for definitions of abbreviations) is luteolytic in midluteal (1.e., d 9 of a 17 d estrous cycle) sheep. However, the pharmacokinetic responses to PGF<sub>2α</sub>-induced luteolysis are not known. This study (Exp. 1 and 2) was conducted to determine several pharmacokinetic responses to two dosing regimens of Lutalyse® (PGF<sub>2α</sub>). Experiment 1 was a 2 x 2 factorial design, with Lutalyse and H/Ox as main effects. Lutalyse (15 mg) was injected i.m., and blood samples were collected, relative to the time of injection, from the vena cava at points cranial and caudal to the uteroovarian vein. Progesterone and PGF<sub>2α</sub>, were measured in blood plasma. The PGF<sub>2α</sub> concentrations were greater in H/Ox and sham H/Ox ewes treated-with Lutalyse® than in control ewes. Peak concentrations of PGF<sub>2α</sub> were greatest in sham H/Ox Lutalyse-treated ewes, indicating that the uterus and(or) ovaries secrete PGF<sub>2α</sub>, in response to exogenous PGF<sub>2α</sub>. In Lutalyse-treated ewes, progesterone concentrations decreased by 50% within 8 h after treatment. The design of Exp. 2 was also a 2 x 2 factorial, with Lutalyse (2 x 5mg at 3 h intervals) and H/Ox as main effects. Prostaglandin F<sub>2α</sub> and PGFM were measured in blood plasma collected, relative to the time of injections, from the vena cava at points cranial and caudal to the uteroovarian vein. The PGF<sub>2α</sub> concentrations were greater in sham H/Ox ewes treated-with Lutalyse than in control ewes. Peak concentrations of PGF<sub>2α</sub> were greater in sham H/Ox than in ewes in all other treatment groups, indicating again that the uterus and(or) ovaries secrete PGF<sub>2α</sub> in response to exogenous PGF<sub>2α</sub> In general, PGFM concentrations increased in a pattern similar to that of PGF<sub>2α</sub> after Lutalyse injection; although there was a short delay of approximately 2 min. Caudal vena caval PGF, concentrations in H/Ox Lutalyse-treated ewes were greater than that after saline injection, which indicates that metabolism may depend on the presence or absence of the uterus and(or) ovaries. In Exp. 1, caudal PGF, concentrations were greater in H/Ox ewes injected with 15 mg of Lutalyse than in ewes in all other treatments . However, in response to 5 mg Lutalyse, caudal PGF<sub>2α</sub> concentrations were greater in sham H/Ox ewes than in all other treatment groups. This indicates that the larger dose in H/Ox ewes supersedes the capacity of the lung and kidney to dispose of PGF<sub>2α</sub>, and PGF<sub>2α</sub> is more tightly regulated in intact ewes. The lungs and kidney are capable of metabolizing the smaller dose of Lutalyse but not the resulting PGF<sub>2α</sub> production in intact ewes. A short validation experiment was conducted to determine the effects of sampling location on progesterone, PGF<sub>2α</sub> and PGFM concentrations. Sampling location did not affect the mean concentration of progesterone or PGFM. However, location affected the mean PGF<sub>2α</sub> concentration. The concentration of PGF<sub>2α</sub>, was greater (P < .05) in saphenous vein and caudal vena caval blood plasma than in jugular plasma. In summary, the uterus and(or) ovaries produce and regulate PGF<sub>2α</sub> concentration in response to Lutalyse. It is speculated that a threshold PGF<sub>2α</sub> concentration or duration of the PGF<sub>2α</sub> peak concentration exists because these PGF<sub>2α</sub>, responses differed in intact Lutalyse-treated and saline-treated ewes in both experiments. The mean cranial PGF<sub>2α</sub> concentration, peak concentration, duration of the peak, increase in PGF<sub>2α</sub> and AUC were greater in response to 15 mg of Lutalyse, although the two smaller doses have been shown to be more efficacious in inducing luteolysis. The second dose of PGF<sub>2α</sub> may act by mimicking pulses of PGF<sub>2α</sub> and initiate the luteolytic cascade two times. === Master of Science
author2 Animal and Poultry Sciences
author_facet Animal and Poultry Sciences
Wade, Dawn E.
author Wade, Dawn E.
author_sort Wade, Dawn E.
title Lutalyse® induces uterine-ovarian PGF₂α release in sheep: a critical component of induced luteolysis
title_short Lutalyse® induces uterine-ovarian PGF₂α release in sheep: a critical component of induced luteolysis
title_full Lutalyse® induces uterine-ovarian PGF₂α release in sheep: a critical component of induced luteolysis
title_fullStr Lutalyse® induces uterine-ovarian PGF₂α release in sheep: a critical component of induced luteolysis
title_full_unstemmed Lutalyse® induces uterine-ovarian PGF₂α release in sheep: a critical component of induced luteolysis
title_sort lutalyse® induces uterine-ovarian pgf₂α release in sheep: a critical component of induced luteolysis
publisher Virginia Tech
publishDate 2014
url http://hdl.handle.net/10919/43803
http://scholar.lib.vt.edu/theses/available/etd-07212009-040504/
work_keys_str_mv AT wadedawne lutalyseinducesuterineovarianpgf2areleaseinsheepacriticalcomponentofinducedluteolysis
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spelling ndltd-VTETD-oai-vtechworks.lib.vt.edu-10919-438032021-05-26T05:48:30Z Lutalyse® induces uterine-ovarian PGF₂α release in sheep: a critical component of induced luteolysis Wade, Dawn E. Animal and Poultry Sciences LD5655.V855 1994.W334 Luteinizing hormone Sheep -- Physiology Exogenous PGF<sub>2α</sub>, (see Appendix I for definitions of abbreviations) is luteolytic in midluteal (1.e., d 9 of a 17 d estrous cycle) sheep. However, the pharmacokinetic responses to PGF<sub>2α</sub>-induced luteolysis are not known. This study (Exp. 1 and 2) was conducted to determine several pharmacokinetic responses to two dosing regimens of Lutalyse® (PGF<sub>2α</sub>). Experiment 1 was a 2 x 2 factorial design, with Lutalyse and H/Ox as main effects. Lutalyse (15 mg) was injected i.m., and blood samples were collected, relative to the time of injection, from the vena cava at points cranial and caudal to the uteroovarian vein. Progesterone and PGF<sub>2α</sub>, were measured in blood plasma. The PGF<sub>2α</sub> concentrations were greater in H/Ox and sham H/Ox ewes treated-with Lutalyse® than in control ewes. Peak concentrations of PGF<sub>2α</sub> were greatest in sham H/Ox Lutalyse-treated ewes, indicating that the uterus and(or) ovaries secrete PGF<sub>2α</sub>, in response to exogenous PGF<sub>2α</sub>. In Lutalyse-treated ewes, progesterone concentrations decreased by 50% within 8 h after treatment. The design of Exp. 2 was also a 2 x 2 factorial, with Lutalyse (2 x 5mg at 3 h intervals) and H/Ox as main effects. Prostaglandin F<sub>2α</sub> and PGFM were measured in blood plasma collected, relative to the time of injections, from the vena cava at points cranial and caudal to the uteroovarian vein. The PGF<sub>2α</sub> concentrations were greater in sham H/Ox ewes treated-with Lutalyse than in control ewes. Peak concentrations of PGF<sub>2α</sub> were greater in sham H/Ox than in ewes in all other treatment groups, indicating again that the uterus and(or) ovaries secrete PGF<sub>2α</sub> in response to exogenous PGF<sub>2α</sub> In general, PGFM concentrations increased in a pattern similar to that of PGF<sub>2α</sub> after Lutalyse injection; although there was a short delay of approximately 2 min. Caudal vena caval PGF, concentrations in H/Ox Lutalyse-treated ewes were greater than that after saline injection, which indicates that metabolism may depend on the presence or absence of the uterus and(or) ovaries. In Exp. 1, caudal PGF, concentrations were greater in H/Ox ewes injected with 15 mg of Lutalyse than in ewes in all other treatments . However, in response to 5 mg Lutalyse, caudal PGF<sub>2α</sub> concentrations were greater in sham H/Ox ewes than in all other treatment groups. This indicates that the larger dose in H/Ox ewes supersedes the capacity of the lung and kidney to dispose of PGF<sub>2α</sub>, and PGF<sub>2α</sub> is more tightly regulated in intact ewes. The lungs and kidney are capable of metabolizing the smaller dose of Lutalyse but not the resulting PGF<sub>2α</sub> production in intact ewes. A short validation experiment was conducted to determine the effects of sampling location on progesterone, PGF<sub>2α</sub> and PGFM concentrations. Sampling location did not affect the mean concentration of progesterone or PGFM. However, location affected the mean PGF<sub>2α</sub> concentration. The concentration of PGF<sub>2α</sub>, was greater (P < .05) in saphenous vein and caudal vena caval blood plasma than in jugular plasma. In summary, the uterus and(or) ovaries produce and regulate PGF<sub>2α</sub> concentration in response to Lutalyse. It is speculated that a threshold PGF<sub>2α</sub> concentration or duration of the PGF<sub>2α</sub> peak concentration exists because these PGF<sub>2α</sub>, responses differed in intact Lutalyse-treated and saline-treated ewes in both experiments. The mean cranial PGF<sub>2α</sub> concentration, peak concentration, duration of the peak, increase in PGF<sub>2α</sub> and AUC were greater in response to 15 mg of Lutalyse, although the two smaller doses have been shown to be more efficacious in inducing luteolysis. The second dose of PGF<sub>2α</sub> may act by mimicking pulses of PGF<sub>2α</sub> and initiate the luteolytic cascade two times. Master of Science 2014-03-14T21:40:47Z 2014-03-14T21:40:47Z 1994 2009-07-21 2009-07-21 2009-07-21 Thesis Text etd-07212009-040504 http://hdl.handle.net/10919/43803 http://scholar.lib.vt.edu/theses/available/etd-07212009-040504/ en OCLC# 30506005 LD5655.V855_1994.W334.pdf In Copyright http://rightsstatements.org/vocab/InC/1.0/ ix, 111 leaves BTD application/pdf application/pdf Virginia Tech