Mechanisms behind intrauterine device-induced luteal persistence in mares
Intrauterine glass balls are used to prevent oestrous signs in sports mares, but the mechanism of action is unknown. It has been suggested that the glass ball can mimic an embryo or act via an induced chronic uterine inflammation and absent or continuous low-grade prostaglandin (PG) release. The pur...
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description | Intrauterine glass balls are used to prevent oestrous signs in sports mares, but the mechanism of action is unknown. It has been suggested that the glass ball can mimic an embryo or act via an induced chronic uterine inflammation and absent or continuous low-grade prostaglandin (PG) release. The purpose of this study was to induce prolonged luteal function in mares using a small intrauterine device (IUD) and to study the mechanisms behind prolonged IUD-induced luteal function. A uterine swab and a biopsy specimen were obtained in early oestrus. A water-filled plastic ball, diameter 20
mm and weight 3.6
g, was inserted into the uterus 2–4 days after ovulation; the control mares underwent similar cervical manipulation without ball insertion. The mares were examined three times per week until day 23 and twice weekly thereafter until they returned to oestrus (transrectal palpation, ultrasonography and progesterone determination). The location of the IUD was recorded and ultrasound scans were video-recorded to assess the frequency of uterine contractions. When the mare returned to oestrus, a uterine swab and biopsy specimen were obtained and the bacteriological, cytological and histological (inflammation and glandular dilation) results compared with the samples obtained before the IUD insertion. The PG F
2α metabolite levels were measured in the plasma of four control mares and eight IUD mares on days 11–16.
The IUD induced a prolonged luteal phase in 75% of the mares (9/12; IUD-P); the mean dioestrous length was 57.0 days. The three mares that did not respond to the IUD (IUD-N) showed a mean dioestrous length of 15.7 days and the 12 control mares 16.1 days. The inflammation and glandular dilation scores were not significantly different in pre- and post-manipulation biopsy specimens. Although locational changes of the IUD were observed, they occurred over very small distances and were mostly limited within the body-bifurcation area. The IUD-N and control mares showed increased uterine contractility 11–16 days post-ovulation, whereas the IUD-P mares did not. The control mares (
n
=
4) and IUD-N mares (
n
=
2) showed increased PG levels from day 14 post-ovulation, while the IUD-P mares (
n
=
6) showed basal levels only. We concluded that the IUD did not cause continuous PG release and suggest that close contact of the IUD with the endometrium may prevent the endometrial cells from releasing PGF
2α. |
doi_str_mv | 10.1016/j.anireprosci.2007.06.010 |
format | Article |
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mm and weight 3.6
g, was inserted into the uterus 2–4 days after ovulation; the control mares underwent similar cervical manipulation without ball insertion. The mares were examined three times per week until day 23 and twice weekly thereafter until they returned to oestrus (transrectal palpation, ultrasonography and progesterone determination). The location of the IUD was recorded and ultrasound scans were video-recorded to assess the frequency of uterine contractions. When the mare returned to oestrus, a uterine swab and biopsy specimen were obtained and the bacteriological, cytological and histological (inflammation and glandular dilation) results compared with the samples obtained before the IUD insertion. The PG F
2α metabolite levels were measured in the plasma of four control mares and eight IUD mares on days 11–16.
The IUD induced a prolonged luteal phase in 75% of the mares (9/12; IUD-P); the mean dioestrous length was 57.0 days. The three mares that did not respond to the IUD (IUD-N) showed a mean dioestrous length of 15.7 days and the 12 control mares 16.1 days. The inflammation and glandular dilation scores were not significantly different in pre- and post-manipulation biopsy specimens. Although locational changes of the IUD were observed, they occurred over very small distances and were mostly limited within the body-bifurcation area. The IUD-N and control mares showed increased uterine contractility 11–16 days post-ovulation, whereas the IUD-P mares did not. The control mares (
n
=
4) and IUD-N mares (
n
=
2) showed increased PG levels from day 14 post-ovulation, while the IUD-P mares (
n
=
6) showed basal levels only. We concluded that the IUD did not cause continuous PG release and suggest that close contact of the IUD with the endometrium may prevent the endometrial cells from releasing PGF
2α.</description><identifier>ISSN: 0378-4320</identifier><identifier>EISSN: 1873-2232</identifier><identifier>DOI: 10.1016/j.anireprosci.2007.06.010</identifier><identifier>PMID: 17643876</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; controlled internal drug release devices ; Corpus Luteum - physiology ; Corpus luteum persistence ; Dinoprost - blood ; endometrium ; Endometrium - physiology ; European Union ; Female ; hormone supplements ; Horses - blood ; Horses - physiology ; induced luteal persistence ; intrauterine administration ; Intrauterine device ; Intrauterine Devices - veterinary ; intrauterine glass balls ; luteal cells ; luteal phase ; luteolysis ; mares ; PGF 2α metabolite ; Progesterone ; Progesterone - blood ; Time Factors ; Uterine contractions</subject><ispartof>Animal reproduction science, 2008-08, Vol.107 (1), p.94-106</ispartof><rights>2007 Elsevier B.V.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c450t-ff1a9431c1f32664edad42b5e507846159fe6862b70413fbbb3fdd0186e61fb13</citedby><cites>FETCH-LOGICAL-c450t-ff1a9431c1f32664edad42b5e507846159fe6862b70413fbbb3fdd0186e61fb13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.anireprosci.2007.06.010$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27922,27923,45993</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17643876$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rivera del Alamo, M.M.</creatorcontrib><creatorcontrib>Reilas, T.</creatorcontrib><creatorcontrib>Kindahl, H.</creatorcontrib><creatorcontrib>Katila, T.</creatorcontrib><title>Mechanisms behind intrauterine device-induced luteal persistence in mares</title><title>Animal reproduction science</title><addtitle>Anim Reprod Sci</addtitle><description>Intrauterine glass balls are used to prevent oestrous signs in sports mares, but the mechanism of action is unknown. It has been suggested that the glass ball can mimic an embryo or act via an induced chronic uterine inflammation and absent or continuous low-grade prostaglandin (PG) release. The purpose of this study was to induce prolonged luteal function in mares using a small intrauterine device (IUD) and to study the mechanisms behind prolonged IUD-induced luteal function. A uterine swab and a biopsy specimen were obtained in early oestrus. A water-filled plastic ball, diameter 20
mm and weight 3.6
g, was inserted into the uterus 2–4 days after ovulation; the control mares underwent similar cervical manipulation without ball insertion. The mares were examined three times per week until day 23 and twice weekly thereafter until they returned to oestrus (transrectal palpation, ultrasonography and progesterone determination). The location of the IUD was recorded and ultrasound scans were video-recorded to assess the frequency of uterine contractions. When the mare returned to oestrus, a uterine swab and biopsy specimen were obtained and the bacteriological, cytological and histological (inflammation and glandular dilation) results compared with the samples obtained before the IUD insertion. The PG F
2α metabolite levels were measured in the plasma of four control mares and eight IUD mares on days 11–16.
The IUD induced a prolonged luteal phase in 75% of the mares (9/12; IUD-P); the mean dioestrous length was 57.0 days. The three mares that did not respond to the IUD (IUD-N) showed a mean dioestrous length of 15.7 days and the 12 control mares 16.1 days. The inflammation and glandular dilation scores were not significantly different in pre- and post-manipulation biopsy specimens. Although locational changes of the IUD were observed, they occurred over very small distances and were mostly limited within the body-bifurcation area. The IUD-N and control mares showed increased uterine contractility 11–16 days post-ovulation, whereas the IUD-P mares did not. The control mares (
n
=
4) and IUD-N mares (
n
=
2) showed increased PG levels from day 14 post-ovulation, while the IUD-P mares (
n
=
6) showed basal levels only. We concluded that the IUD did not cause continuous PG release and suggest that close contact of the IUD with the endometrium may prevent the endometrial cells from releasing PGF
2α.</description><subject>Animals</subject><subject>controlled internal drug release devices</subject><subject>Corpus Luteum - physiology</subject><subject>Corpus luteum persistence</subject><subject>Dinoprost - blood</subject><subject>endometrium</subject><subject>Endometrium - physiology</subject><subject>European Union</subject><subject>Female</subject><subject>hormone supplements</subject><subject>Horses - blood</subject><subject>Horses - physiology</subject><subject>induced luteal persistence</subject><subject>intrauterine administration</subject><subject>Intrauterine device</subject><subject>Intrauterine Devices - veterinary</subject><subject>intrauterine glass balls</subject><subject>luteal cells</subject><subject>luteal phase</subject><subject>luteolysis</subject><subject>mares</subject><subject>PGF 2α metabolite</subject><subject>Progesterone</subject><subject>Progesterone - blood</subject><subject>Time Factors</subject><subject>Uterine contractions</subject><issn>0378-4320</issn><issn>1873-2232</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkMFO3DAQhq0KVBboK7Thwi1hbCd2cqxWQJGoeoA9W4497nqVzW7tBKlvz6x2pXLsydLom_8ff4zdcKg4cHW3qewYE-7TLrtYCQBdgaqAwye24K2WpRBSnLEFSN2WtRRwwS5z3gCBSnWf2QXXqpatVgv29BPdmtLyNhc9ruPoizhOyc4Tpjhi4fEtOixpPjv0xUBzOxR7TDnmCUeHhBdbmzBfs_Ngh4xfTu8VWz3cvy5_lM-_Hp-W359LVzcwlSFw29WSOx6kUKpGb30t-gYb0G2teNMFVK0SvYaay9D3vQzeA28VKh56Lq_Y7TGXvv9nxjyZbcwOh8GOuJuz0aAb0TQdgd0RdOQpJwxmnyKd-tdwMAePZmM-eDQHjwaUIY-0-_VUMvdb9P82T-II-HYEgt0Z-zvFbFYvArgE6IASBBHLI4Ek4y1iMlRyMOap0k3G7-J_HPIOxJyUMQ</recordid><startdate>20080801</startdate><enddate>20080801</enddate><creator>Rivera del Alamo, M.M.</creator><creator>Reilas, T.</creator><creator>Kindahl, H.</creator><creator>Katila, T.</creator><general>Elsevier B.V</general><general>[Amsterdam]: Elsevier Science</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>20080801</creationdate><title>Mechanisms behind intrauterine device-induced luteal persistence in mares</title><author>Rivera del Alamo, M.M. ; Reilas, T. ; Kindahl, H. ; Katila, T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c450t-ff1a9431c1f32664edad42b5e507846159fe6862b70413fbbb3fdd0186e61fb13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animals</topic><topic>controlled internal drug release devices</topic><topic>Corpus Luteum - physiology</topic><topic>Corpus luteum persistence</topic><topic>Dinoprost - blood</topic><topic>endometrium</topic><topic>Endometrium - physiology</topic><topic>European Union</topic><topic>Female</topic><topic>hormone supplements</topic><topic>Horses - blood</topic><topic>Horses - physiology</topic><topic>induced luteal persistence</topic><topic>intrauterine administration</topic><topic>Intrauterine device</topic><topic>Intrauterine Devices - veterinary</topic><topic>intrauterine glass balls</topic><topic>luteal cells</topic><topic>luteal phase</topic><topic>luteolysis</topic><topic>mares</topic><topic>PGF 2α metabolite</topic><topic>Progesterone</topic><topic>Progesterone - blood</topic><topic>Time Factors</topic><topic>Uterine contractions</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rivera del Alamo, M.M.</creatorcontrib><creatorcontrib>Reilas, T.</creatorcontrib><creatorcontrib>Kindahl, H.</creatorcontrib><creatorcontrib>Katila, T.</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>Animal reproduction science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rivera del Alamo, M.M.</au><au>Reilas, T.</au><au>Kindahl, H.</au><au>Katila, T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mechanisms behind intrauterine device-induced luteal persistence in mares</atitle><jtitle>Animal reproduction science</jtitle><addtitle>Anim Reprod Sci</addtitle><date>2008-08-01</date><risdate>2008</risdate><volume>107</volume><issue>1</issue><spage>94</spage><epage>106</epage><pages>94-106</pages><issn>0378-4320</issn><eissn>1873-2232</eissn><abstract>Intrauterine glass balls are used to prevent oestrous signs in sports mares, but the mechanism of action is unknown. It has been suggested that the glass ball can mimic an embryo or act via an induced chronic uterine inflammation and absent or continuous low-grade prostaglandin (PG) release. The purpose of this study was to induce prolonged luteal function in mares using a small intrauterine device (IUD) and to study the mechanisms behind prolonged IUD-induced luteal function. A uterine swab and a biopsy specimen were obtained in early oestrus. A water-filled plastic ball, diameter 20
mm and weight 3.6
g, was inserted into the uterus 2–4 days after ovulation; the control mares underwent similar cervical manipulation without ball insertion. The mares were examined three times per week until day 23 and twice weekly thereafter until they returned to oestrus (transrectal palpation, ultrasonography and progesterone determination). The location of the IUD was recorded and ultrasound scans were video-recorded to assess the frequency of uterine contractions. When the mare returned to oestrus, a uterine swab and biopsy specimen were obtained and the bacteriological, cytological and histological (inflammation and glandular dilation) results compared with the samples obtained before the IUD insertion. The PG F
2α metabolite levels were measured in the plasma of four control mares and eight IUD mares on days 11–16.
The IUD induced a prolonged luteal phase in 75% of the mares (9/12; IUD-P); the mean dioestrous length was 57.0 days. The three mares that did not respond to the IUD (IUD-N) showed a mean dioestrous length of 15.7 days and the 12 control mares 16.1 days. The inflammation and glandular dilation scores were not significantly different in pre- and post-manipulation biopsy specimens. Although locational changes of the IUD were observed, they occurred over very small distances and were mostly limited within the body-bifurcation area. The IUD-N and control mares showed increased uterine contractility 11–16 days post-ovulation, whereas the IUD-P mares did not. The control mares (
n
=
4) and IUD-N mares (
n
=
2) showed increased PG levels from day 14 post-ovulation, while the IUD-P mares (
n
=
6) showed basal levels only. We concluded that the IUD did not cause continuous PG release and suggest that close contact of the IUD with the endometrium may prevent the endometrial cells from releasing PGF
2α.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>17643876</pmid><doi>10.1016/j.anireprosci.2007.06.010</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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source | Elsevier ScienceDirect Journals Complete - AutoHoldings; MEDLINE |
subjects | Animals controlled internal drug release devices Corpus Luteum - physiology Corpus luteum persistence Dinoprost - blood endometrium Endometrium - physiology European Union Female hormone supplements Horses - blood Horses - physiology induced luteal persistence intrauterine administration Intrauterine device Intrauterine Devices - veterinary intrauterine glass balls luteal cells luteal phase luteolysis mares PGF 2α metabolite Progesterone Progesterone - blood Time Factors Uterine contractions |
title | Mechanisms behind intrauterine device-induced luteal persistence in mares |
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