Inhibition of uterine contractility in labor
Uterine contractility was recorded by the direct electronic method in 4 groups of 12 women in labor, in order to study the inhibitory effect of: (1) pregnenolone sulfate, precursor of placental progesterone, expected to block the sensitivity of the myometrial cell; (2) ethanol, known to inhibit the...
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Veröffentlicht in: | American journal of obstetrics and gynecology 1971-12, Vol.111 (7), p.874-885 |
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creator | Bieniarz, Joseph Burd, Laurence Motew, Martin Scommegna, Antonio Lin, Susan Wineman, Catherine Seals, Chresteen |
description | Uterine contractility was recorded by the direct electronic method in 4 groups of 12 women in labor, in order to study the inhibitory effect of: (1) pregnenolone sulfate, precursor of placental progesterone, expected to block the sensitivity of the myometrial cell; (2) ethanol, known to inhibit the release of oxytocin; (3) rapid infusion of 1,000 ml. 5 per cent dextrose, used as the vehicle; and to compare these effects with that of all these factors, acting concomitantly through different mechanisms. Pregnenolone sulfate depressed the frequency of contractions to 67 per cent ± 5.7∗ and their activity to 75 per cent ± 8.0. The effect was immediate but transient. The effect of ethanol was delayed but prolonged and more marked (62 per cent ± 6.9 and 69 per cent ± 1.38, respectively). Rapid infusion of 5 per cent dextrose had a slight but prolonged inhibitory effect (93 per cent ± 5.7 and 83.1 per cent ± 4.1), attributed to the Henry-Gauer reflex which blocked oxytocin release. Neither of these treatments affected the intensity of contractions. The most marked synergistic effect was obtained by the combined pregnenolone-ethanol-dextrose treatment. It was immediate like pregnenolone and prolonged like ethanol; it inhibited not only the frequency (63 per cent ± 7.0) and activity (45 per cent ± 6.3) but also the intensity of uterine contractions (72 per cent ±8.6), although the latter effect tended to recover rapidly. Inhibited uterine activity was related to the elevated plasma progesterone level only during the combined treatment, not during other treatments, when inhibited uterine contractility was related to elevated plasma pregnenolone or ethanol levels, while the progesterone level remained unchanged. |
doi_str_mv | 10.1016/0002-9378(71)90942-2 |
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Pregnenolone sulfate depressed the frequency of contractions to 67 per cent ± 5.7∗ and their activity to 75 per cent ± 8.0. The effect was immediate but transient. The effect of ethanol was delayed but prolonged and more marked (62 per cent ± 6.9 and 69 per cent ± 1.38, respectively). Rapid infusion of 5 per cent dextrose had a slight but prolonged inhibitory effect (93 per cent ± 5.7 and 83.1 per cent ± 4.1), attributed to the Henry-Gauer reflex which blocked oxytocin release. Neither of these treatments affected the intensity of contractions. The most marked synergistic effect was obtained by the combined pregnenolone-ethanol-dextrose treatment. It was immediate like pregnenolone and prolonged like ethanol; it inhibited not only the frequency (63 per cent ± 7.0) and activity (45 per cent ± 6.3) but also the intensity of uterine contractions (72 per cent ±8.6), although the latter effect tended to recover rapidly. Inhibited uterine activity was related to the elevated plasma progesterone level only during the combined treatment, not during other treatments, when inhibited uterine contractility was related to elevated plasma pregnenolone or ethanol levels, while the progesterone level remained unchanged.</description><identifier>ISSN: 0002-9378</identifier><identifier>EISSN: 1097-6868</identifier><identifier>DOI: 10.1016/0002-9378(71)90942-2</identifier><identifier>PMID: 5118026</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adolescent ; Adult ; Amniotic Fluid ; Apgar Score ; Blood Pressure ; Blood Volume ; Ethanol - blood ; Ethanol - pharmacology ; Female ; Fetal Heart ; Gestational Age ; Glucose - pharmacology ; Heart Rate ; Humans ; Infant, Newborn ; Labor, Obstetric ; Muscle Contraction - drug effects ; Oxytocin - antagonists & inhibitors ; Parity ; Pregnancy ; Pregnenolone - blood ; Pregnenolone - pharmacology ; Progesterone - blood ; Uterus - drug effects ; Uterus - metabolism</subject><ispartof>American journal of obstetrics and gynecology, 1971-12, Vol.111 (7), p.874-885</ispartof><rights>1971</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c423t-2fa7bd73f1800a38948457e412264b28e9373416df771a80060e1c2d8f76d9053</citedby><cites>FETCH-LOGICAL-c423t-2fa7bd73f1800a38948457e412264b28e9373416df771a80060e1c2d8f76d9053</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/0002937871909422$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/5118026$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bieniarz, Joseph</creatorcontrib><creatorcontrib>Burd, Laurence</creatorcontrib><creatorcontrib>Motew, Martin</creatorcontrib><creatorcontrib>Scommegna, Antonio</creatorcontrib><creatorcontrib>Lin, Susan</creatorcontrib><creatorcontrib>Wineman, Catherine</creatorcontrib><creatorcontrib>Seals, Chresteen</creatorcontrib><title>Inhibition of uterine contractility in labor</title><title>American journal of obstetrics and gynecology</title><addtitle>Am J Obstet Gynecol</addtitle><description>Uterine contractility was recorded by the direct electronic method in 4 groups of 12 women in labor, in order to study the inhibitory effect of: (1) pregnenolone sulfate, precursor of placental progesterone, expected to block the sensitivity of the myometrial cell; (2) ethanol, known to inhibit the release of oxytocin; (3) rapid infusion of 1,000 ml. 5 per cent dextrose, used as the vehicle; and to compare these effects with that of all these factors, acting concomitantly through different mechanisms. Pregnenolone sulfate depressed the frequency of contractions to 67 per cent ± 5.7∗ and their activity to 75 per cent ± 8.0. The effect was immediate but transient. The effect of ethanol was delayed but prolonged and more marked (62 per cent ± 6.9 and 69 per cent ± 1.38, respectively). Rapid infusion of 5 per cent dextrose had a slight but prolonged inhibitory effect (93 per cent ± 5.7 and 83.1 per cent ± 4.1), attributed to the Henry-Gauer reflex which blocked oxytocin release. Neither of these treatments affected the intensity of contractions. The most marked synergistic effect was obtained by the combined pregnenolone-ethanol-dextrose treatment. It was immediate like pregnenolone and prolonged like ethanol; it inhibited not only the frequency (63 per cent ± 7.0) and activity (45 per cent ± 6.3) but also the intensity of uterine contractions (72 per cent ±8.6), although the latter effect tended to recover rapidly. Inhibited uterine activity was related to the elevated plasma progesterone level only during the combined treatment, not during other treatments, when inhibited uterine contractility was related to elevated plasma pregnenolone or ethanol levels, while the progesterone level remained unchanged.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Amniotic Fluid</subject><subject>Apgar Score</subject><subject>Blood Pressure</subject><subject>Blood Volume</subject><subject>Ethanol - blood</subject><subject>Ethanol - pharmacology</subject><subject>Female</subject><subject>Fetal Heart</subject><subject>Gestational Age</subject><subject>Glucose - pharmacology</subject><subject>Heart Rate</subject><subject>Humans</subject><subject>Infant, Newborn</subject><subject>Labor, Obstetric</subject><subject>Muscle Contraction - drug effects</subject><subject>Oxytocin - antagonists & inhibitors</subject><subject>Parity</subject><subject>Pregnancy</subject><subject>Pregnenolone - blood</subject><subject>Pregnenolone - pharmacology</subject><subject>Progesterone - blood</subject><subject>Uterus - drug effects</subject><subject>Uterus - metabolism</subject><issn>0002-9378</issn><issn>1097-6868</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1971</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9UE1LxDAQDaKs6-o_UOhJFKxm0jRJL4IsfiwseNFzSNMpRrqNJllh_72tu-zR0zDM-5j3CDkHegsUxB2llOVVIdWVhOuKVpzl7IBMgVYyF0qoQzLdQ47JSYyf48oqNiGTEkBRJqbkZtF_uNol5_vMt9k6YXA9Ztb3KRibXOfSJnN91pnah1Ny1Jou4tluzsj70-Pb_CVfvj4v5g_L3HJWpJy1RtaNLNrBg5pCVVzxUiIHxgSvmcLho4KDaFopwQwYQREsa1QrRVPRspiRy63uV_Dfa4xJr1y02HWmR7-OWgGUUvFiAPIt0AYfY8BWfwW3MmGjgeqxJD1G1mMDWoL-K0mzgXax01_XK2z2pF0rw_1-e8ch5I_DoKN12FtsXECbdOPd_wa_eXpziw</recordid><startdate>19711201</startdate><enddate>19711201</enddate><creator>Bieniarz, Joseph</creator><creator>Burd, Laurence</creator><creator>Motew, Martin</creator><creator>Scommegna, Antonio</creator><creator>Lin, Susan</creator><creator>Wineman, Catherine</creator><creator>Seals, Chresteen</creator><general>Elsevier Inc</general><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>19711201</creationdate><title>Inhibition of uterine contractility in labor</title><author>Bieniarz, Joseph ; Burd, Laurence ; Motew, Martin ; Scommegna, Antonio ; Lin, Susan ; Wineman, Catherine ; Seals, Chresteen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c423t-2fa7bd73f1800a38948457e412264b28e9373416df771a80060e1c2d8f76d9053</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1971</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Amniotic Fluid</topic><topic>Apgar Score</topic><topic>Blood Pressure</topic><topic>Blood Volume</topic><topic>Ethanol - blood</topic><topic>Ethanol - pharmacology</topic><topic>Female</topic><topic>Fetal Heart</topic><topic>Gestational Age</topic><topic>Glucose - pharmacology</topic><topic>Heart Rate</topic><topic>Humans</topic><topic>Infant, Newborn</topic><topic>Labor, Obstetric</topic><topic>Muscle Contraction - drug effects</topic><topic>Oxytocin - antagonists & inhibitors</topic><topic>Parity</topic><topic>Pregnancy</topic><topic>Pregnenolone - blood</topic><topic>Pregnenolone - pharmacology</topic><topic>Progesterone - blood</topic><topic>Uterus - drug effects</topic><topic>Uterus - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bieniarz, Joseph</creatorcontrib><creatorcontrib>Burd, Laurence</creatorcontrib><creatorcontrib>Motew, Martin</creatorcontrib><creatorcontrib>Scommegna, Antonio</creatorcontrib><creatorcontrib>Lin, Susan</creatorcontrib><creatorcontrib>Wineman, Catherine</creatorcontrib><creatorcontrib>Seals, Chresteen</creatorcontrib><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>American journal of obstetrics and gynecology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bieniarz, Joseph</au><au>Burd, Laurence</au><au>Motew, Martin</au><au>Scommegna, Antonio</au><au>Lin, Susan</au><au>Wineman, Catherine</au><au>Seals, Chresteen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inhibition of uterine contractility in labor</atitle><jtitle>American journal of obstetrics and gynecology</jtitle><addtitle>Am J Obstet Gynecol</addtitle><date>1971-12-01</date><risdate>1971</risdate><volume>111</volume><issue>7</issue><spage>874</spage><epage>885</epage><pages>874-885</pages><issn>0002-9378</issn><eissn>1097-6868</eissn><abstract>Uterine contractility was recorded by the direct electronic method in 4 groups of 12 women in labor, in order to study the inhibitory effect of: (1) pregnenolone sulfate, precursor of placental progesterone, expected to block the sensitivity of the myometrial cell; (2) ethanol, known to inhibit the release of oxytocin; (3) rapid infusion of 1,000 ml. 5 per cent dextrose, used as the vehicle; and to compare these effects with that of all these factors, acting concomitantly through different mechanisms. Pregnenolone sulfate depressed the frequency of contractions to 67 per cent ± 5.7∗ and their activity to 75 per cent ± 8.0. The effect was immediate but transient. The effect of ethanol was delayed but prolonged and more marked (62 per cent ± 6.9 and 69 per cent ± 1.38, respectively). Rapid infusion of 5 per cent dextrose had a slight but prolonged inhibitory effect (93 per cent ± 5.7 and 83.1 per cent ± 4.1), attributed to the Henry-Gauer reflex which blocked oxytocin release. Neither of these treatments affected the intensity of contractions. The most marked synergistic effect was obtained by the combined pregnenolone-ethanol-dextrose treatment. It was immediate like pregnenolone and prolonged like ethanol; it inhibited not only the frequency (63 per cent ± 7.0) and activity (45 per cent ± 6.3) but also the intensity of uterine contractions (72 per cent ±8.6), although the latter effect tended to recover rapidly. Inhibited uterine activity was related to the elevated plasma progesterone level only during the combined treatment, not during other treatments, when inhibited uterine contractility was related to elevated plasma pregnenolone or ethanol levels, while the progesterone level remained unchanged.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>5118026</pmid><doi>10.1016/0002-9378(71)90942-2</doi><tpages>12</tpages></addata></record> |
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subjects | Adolescent Adult Amniotic Fluid Apgar Score Blood Pressure Blood Volume Ethanol - blood Ethanol - pharmacology Female Fetal Heart Gestational Age Glucose - pharmacology Heart Rate Humans Infant, Newborn Labor, Obstetric Muscle Contraction - drug effects Oxytocin - antagonists & inhibitors Parity Pregnancy Pregnenolone - blood Pregnenolone - pharmacology Progesterone - blood Uterus - drug effects Uterus - metabolism |
title | Inhibition of uterine contractility in labor |
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