Endometrial inositol phosphate turnover in pigs is reduced during pregnancy and estradiol-induced pseudopregnancy

Three experiments were conducted to examine inositol phosphate (IP) turnover in response to treatments applied in vitro to endometrium from cyclic (CYC), pregnant (PREG) and estradiol-induced pseudopregnant (PSP) gilts. In Exp. 1, treatments (in 25 microliters .1 M NaHCO3) were 1) control (NaHCO3),...

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Veröffentlicht in:Journal of animal science 1990-12, Vol.68 (12), p.4285-4291
Hauptverfasser: Mirando, M.A. (University of Florida, Gainesville), Leen, M.P.J.M, Beers, S, Harney, J.P, Bazer, F.W
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container_end_page 4291
container_issue 12
container_start_page 4285
container_title Journal of animal science
container_volume 68
creator Mirando, M.A. (University of Florida, Gainesville)
Leen, M.P.J.M
Beers, S
Harney, J.P
Bazer, F.W
description Three experiments were conducted to examine inositol phosphate (IP) turnover in response to treatments applied in vitro to endometrium from cyclic (CYC), pregnant (PREG) and estradiol-induced pseudopregnant (PSP) gilts. In Exp. 1, treatments (in 25 microliters .1 M NaHCO3) were 1) control (NaHCO3), 2) 125 ng oxytocin, 3) .25 micrograms prolactin, 4) 2.5 micrograms prolactin and 5) 5 micrograms pig conceptus secretory proteins (pCSP). Basal IP turnover on d 14 (estrus = d 0) for CYC was 3.9 to 5.0-fold greater than for PREG gilts and .6 to 1.1-fold greater than for PSP gilts (P less than .05). Oxytocin increased IP turnover 23 to 42% in CYC gilts (P less than .05), but not in PREG or PSP gilts. The treatment x reproductive status interaction (P less than .05) indicated that pCSP increased IP turnover 74 to 140% in PREG gilts but decreased it 18 to 22% in CYC and 17 to 50% in PSP gilts. In Exp. 2, treatments were applied in a 2 x 2 x 2 arrangement: 1) 0 or 125 ng oxytocin; 2) 0 or 2.5 micrograms prolactin and 3) 0 or 5 micrograms pCSP. Basal IP turnover on d 14 was 3.3 to 5.4-fold greater (P less than .05) in CYC than in PSP gilts and was affected by interaction (P less than .05) of pCSP and prolactin. Inositol phosphate turnover was increased by prolactin (12 to 22%) and by pCSP (7 to 34%) but, when combined, the stimulatory effects of each were eliminated.
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In Exp. 1, treatments (in 25 microliters .1 M NaHCO3) were 1) control (NaHCO3), 2) 125 ng oxytocin, 3) .25 micrograms prolactin, 4) 2.5 micrograms prolactin and 5) 5 micrograms pig conceptus secretory proteins (pCSP). Basal IP turnover on d 14 (estrus = d 0) for CYC was 3.9 to 5.0-fold greater than for PREG gilts and .6 to 1.1-fold greater than for PSP gilts (P less than .05). Oxytocin increased IP turnover 23 to 42% in CYC gilts (P less than .05), but not in PREG or PSP gilts. The treatment x reproductive status interaction (P less than .05) indicated that pCSP increased IP turnover 74 to 140% in PREG gilts but decreased it 18 to 22% in CYC and 17 to 50% in PSP gilts. In Exp. 2, treatments were applied in a 2 x 2 x 2 arrangement: 1) 0 or 125 ng oxytocin; 2) 0 or 2.5 micrograms prolactin and 3) 0 or 5 micrograms pCSP. Basal IP turnover on d 14 was 3.3 to 5.4-fold greater (P less than .05) in CYC than in PSP gilts and was affected by interaction (P less than .05) of pCSP and prolactin. 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In Exp. 1, treatments (in 25 microliters .1 M NaHCO3) were 1) control (NaHCO3), 2) 125 ng oxytocin, 3) .25 micrograms prolactin, 4) 2.5 micrograms prolactin and 5) 5 micrograms pig conceptus secretory proteins (pCSP). Basal IP turnover on d 14 (estrus = d 0) for CYC was 3.9 to 5.0-fold greater than for PREG gilts and .6 to 1.1-fold greater than for PSP gilts (P less than .05). Oxytocin increased IP turnover 23 to 42% in CYC gilts (P less than .05), but not in PREG or PSP gilts. The treatment x reproductive status interaction (P less than .05) indicated that pCSP increased IP turnover 74 to 140% in PREG gilts but decreased it 18 to 22% in CYC and 17 to 50% in PSP gilts. In Exp. 2, treatments were applied in a 2 x 2 x 2 arrangement: 1) 0 or 125 ng oxytocin; 2) 0 or 2.5 micrograms prolactin and 3) 0 or 5 micrograms pCSP. Basal IP turnover on d 14 was 3.3 to 5.4-fold greater (P less than .05) in CYC than in PSP gilts and was affected by interaction (P less than .05) of pCSP and prolactin. Inositol phosphate turnover was increased by prolactin (12 to 22%) and by pCSP (7 to 34%) but, when combined, the stimulatory effects of each were eliminated.</description><subject>Animals</subject><subject>AZUCARES FOSFATOS</subject><subject>CERDAS</subject><subject>Endometrium - drug effects</subject><subject>Endometrium - metabolism</subject><subject>Estradiol - pharmacology</subject><subject>ESTROGENOS</subject><subject>Estrus - metabolism</subject><subject>Female</subject><subject>Fetal Proteins - pharmacology</subject><subject>FETO</subject><subject>FOETUS</subject><subject>GESTACION</subject><subject>GESTATION</subject><subject>INOSITOL</subject><subject>Inositol Phosphates - metabolism</subject><subject>OCYTOCINE</subject><subject>OESTROGENE</subject><subject>OESTROGENS</subject><subject>Organ Culture Techniques</subject><subject>OXITOCINA</subject><subject>OXYTOCIN</subject><subject>Oxytocin - pharmacology</subject><subject>PREGNANCY</subject><subject>Pregnancy, Animal - metabolism</subject><subject>PROLACTIN</subject><subject>Prolactin - pharmacology</subject><subject>PROLACTINA</subject><subject>PROLACTINE</subject><subject>PROTEINAS</subject><subject>PROTEINE</subject><subject>PROTEINS</subject><subject>PSEUDOGESTATION</subject><subject>PSEUDOPREGNANCY</subject><subject>Pseudopregnancy - metabolism</subject><subject>Pseudopregnancy - veterinary</subject><subject>SEUDOGESTACION</subject><subject>SOWS</subject><subject>SUCRE PHOSPHATE</subject><subject>SUGAR PHOSPHATES</subject><subject>Swine - metabolism</subject><subject>Swine Diseases - metabolism</subject><subject>TRUIE</subject><subject>UTERO</subject><subject>UTERUS</subject><issn>0021-8812</issn><issn>1525-3163</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kM1L5DAYh8Oi6KzudQ8LQk7uqWPeZNKmRxH3A4Q9qOeQSd52Im1Sk3bV_94OHeaUw_O8P8JDyHdgay55dQN1zdalAr7hSr5_ISuQXBYCSnFCVoxxKNQMz8nXnF8YAy5reUbOOFelLOsVeb0PLvY4Jm866kPMfowdHXYxDzszIh2nFOJ_TDOjg28z9ZkmdJNFR92UfGjpkLANJtgPaoKjmMdknI9d4cOiDRknF4_WJTltTJfx2-G9IM-_7p_u_hQP_37_vbt9KKzYwFgIVzOrHLcCUdoanLIgnHWgqtJaUwKrDBhToRWMbyuutpWxdeOwAa5Aorgg18vukOLrNH9L9z5b7DoTME5ZK8blRqhqFteLaFPMOWGjh-R7kz40ML1vrPeN9bHxfHB1WJ62Pbqjfog6858L3_l29-YT6tybrptt0C8ml0oD1_up2fyxmI2J2rTJZ_38WAMIqYT4BCp6kBE</recordid><startdate>19901201</startdate><enddate>19901201</enddate><creator>Mirando, M.A. (University of Florida, Gainesville)</creator><creator>Leen, M.P.J.M</creator><creator>Beers, S</creator><creator>Harney, J.P</creator><creator>Bazer, F.W</creator><general>Am Soc Animal Sci</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19901201</creationdate><title>Endometrial inositol phosphate turnover in pigs is reduced during pregnancy and estradiol-induced pseudopregnancy</title><author>Mirando, M.A. (University of Florida, Gainesville) ; Leen, M.P.J.M ; Beers, S ; Harney, J.P ; Bazer, F.W</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c341t-3d90c8d2c3ee5c91d8c13dcd1876cca6107a1aa7ec302b728b7ac9fdef12815e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>Animals</topic><topic>AZUCARES FOSFATOS</topic><topic>CERDAS</topic><topic>Endometrium - drug effects</topic><topic>Endometrium - metabolism</topic><topic>Estradiol - pharmacology</topic><topic>ESTROGENOS</topic><topic>Estrus - metabolism</topic><topic>Female</topic><topic>Fetal Proteins - pharmacology</topic><topic>FETO</topic><topic>FOETUS</topic><topic>GESTACION</topic><topic>GESTATION</topic><topic>INOSITOL</topic><topic>Inositol Phosphates - metabolism</topic><topic>OCYTOCINE</topic><topic>OESTROGENE</topic><topic>OESTROGENS</topic><topic>Organ Culture Techniques</topic><topic>OXITOCINA</topic><topic>OXYTOCIN</topic><topic>Oxytocin - pharmacology</topic><topic>PREGNANCY</topic><topic>Pregnancy, Animal - metabolism</topic><topic>PROLACTIN</topic><topic>Prolactin - pharmacology</topic><topic>PROLACTINA</topic><topic>PROLACTINE</topic><topic>PROTEINAS</topic><topic>PROTEINE</topic><topic>PROTEINS</topic><topic>PSEUDOGESTATION</topic><topic>PSEUDOPREGNANCY</topic><topic>Pseudopregnancy - metabolism</topic><topic>Pseudopregnancy - veterinary</topic><topic>SEUDOGESTACION</topic><topic>SOWS</topic><topic>SUCRE PHOSPHATE</topic><topic>SUGAR PHOSPHATES</topic><topic>Swine - metabolism</topic><topic>Swine Diseases - metabolism</topic><topic>TRUIE</topic><topic>UTERO</topic><topic>UTERUS</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mirando, M.A. (University of Florida, Gainesville)</creatorcontrib><creatorcontrib>Leen, M.P.J.M</creatorcontrib><creatorcontrib>Beers, S</creatorcontrib><creatorcontrib>Harney, J.P</creatorcontrib><creatorcontrib>Bazer, F.W</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of animal science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mirando, M.A. (University of Florida, Gainesville)</au><au>Leen, M.P.J.M</au><au>Beers, S</au><au>Harney, J.P</au><au>Bazer, F.W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Endometrial inositol phosphate turnover in pigs is reduced during pregnancy and estradiol-induced pseudopregnancy</atitle><jtitle>Journal of animal science</jtitle><addtitle>J Anim Sci</addtitle><date>1990-12-01</date><risdate>1990</risdate><volume>68</volume><issue>12</issue><spage>4285</spage><epage>4291</epage><pages>4285-4291</pages><issn>0021-8812</issn><eissn>1525-3163</eissn><abstract>Three experiments were conducted to examine inositol phosphate (IP) turnover in response to treatments applied in vitro to endometrium from cyclic (CYC), pregnant (PREG) and estradiol-induced pseudopregnant (PSP) gilts. In Exp. 1, treatments (in 25 microliters .1 M NaHCO3) were 1) control (NaHCO3), 2) 125 ng oxytocin, 3) .25 micrograms prolactin, 4) 2.5 micrograms prolactin and 5) 5 micrograms pig conceptus secretory proteins (pCSP). Basal IP turnover on d 14 (estrus = d 0) for CYC was 3.9 to 5.0-fold greater than for PREG gilts and .6 to 1.1-fold greater than for PSP gilts (P less than .05). Oxytocin increased IP turnover 23 to 42% in CYC gilts (P less than .05), but not in PREG or PSP gilts. The treatment x reproductive status interaction (P less than .05) indicated that pCSP increased IP turnover 74 to 140% in PREG gilts but decreased it 18 to 22% in CYC and 17 to 50% in PSP gilts. In Exp. 2, treatments were applied in a 2 x 2 x 2 arrangement: 1) 0 or 125 ng oxytocin; 2) 0 or 2.5 micrograms prolactin and 3) 0 or 5 micrograms pCSP. Basal IP turnover on d 14 was 3.3 to 5.4-fold greater (P less than .05) in CYC than in PSP gilts and was affected by interaction (P less than .05) of pCSP and prolactin. Inositol phosphate turnover was increased by prolactin (12 to 22%) and by pCSP (7 to 34%) but, when combined, the stimulatory effects of each were eliminated.</abstract><cop>United States</cop><pub>Am Soc Animal Sci</pub><pmid>2286569</pmid><doi>10.2527/1990.68124285x</doi><tpages>7</tpages></addata></record>
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subjects Animals
AZUCARES FOSFATOS
CERDAS
Endometrium - drug effects
Endometrium - metabolism
Estradiol - pharmacology
ESTROGENOS
Estrus - metabolism
Female
Fetal Proteins - pharmacology
FETO
FOETUS
GESTACION
GESTATION
INOSITOL
Inositol Phosphates - metabolism
OCYTOCINE
OESTROGENE
OESTROGENS
Organ Culture Techniques
OXITOCINA
OXYTOCIN
Oxytocin - pharmacology
PREGNANCY
Pregnancy, Animal - metabolism
PROLACTIN
Prolactin - pharmacology
PROLACTINA
PROLACTINE
PROTEINAS
PROTEINE
PROTEINS
PSEUDOGESTATION
PSEUDOPREGNANCY
Pseudopregnancy - metabolism
Pseudopregnancy - veterinary
SEUDOGESTACION
SOWS
SUCRE PHOSPHATE
SUGAR PHOSPHATES
Swine - metabolism
Swine Diseases - metabolism
TRUIE
UTERO
UTERUS
title Endometrial inositol phosphate turnover in pigs is reduced during pregnancy and estradiol-induced pseudopregnancy
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