Estrous cycle characterisation and artificial insemination using frozen–thawed spermatozoa in the bottlenose dolphin (Tursiops truncatus)
The reproductive endocrinology of the bottlenose dolphin, Tursiops truncatus, was characterized to facilitate the development of artificial insemination using cryopreserved spermatozoa. Specific objectives were: (i) to determine the excretory dynamics of urinary luteinizing hormone (LH) and ovarian...
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Veröffentlicht in: | Reproduction (Cambridge, England) England), 2005-05, Vol.129 (5), p.659-674 |
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description | The reproductive endocrinology of the bottlenose dolphin, Tursiops truncatus, was characterized to facilitate the development of artificial insemination using cryopreserved spermatozoa. Specific objectives were: (i) to determine the excretory dynamics of urinary luteinizing hormone (LH) and ovarian steroid metabolites during the estrous cycle; (ii) to evaluate the effect of an exogenously administered synthetic progesterone analog (altrenogest) on reproductive hormone excretion; (iii) to correlate follicular growth and ovulation (as determined by transabdominal ultrasound) to urinary LH and ovarian steroid metabolites; (iv) examine the in vivo fertilisation capacity of cryopreserved semen, and (v) to develop an intrauterine insemination technique. Based on urinary endocrine monitoring of natural estrous cycles (2 consecutive cycles) and nine post altrenogest cycles in ten females, estrous cycles were found to be 36 days long and comprised of an 8 day and 19 day follicular and luteal phase, respectively. Peak estrogen conjugates (EC; 5.4 ± 3.8 ng/mg creatinine (Cr)) occurred 8 h prior to the LH surge (70.9 ± 115.7 ng/mg Cr). The time of ovulation, as determined by ultrasonography, occurred 32.1 ± 8.9 h and 24.3 ± 7.0 h after the onset of the LH surge and LH peak, respectively. Mean preovulatory follicular diameter and circumference were 2.1 ± 0.5 cm and 6.5 ± 1.5 cm, respectively. Of the 27 estrous synchronisation attempts, 13 resulted in an ovulatory cycle, with ovulation occurring 21 days post-altrenogest treatment. Intrauterine (4 of 5) and intracornual (1 of 3) inseminations conducted across eight estrous cycles resulted in five pregnancies (63%), one pregnancy resulted from the use of liquid stored semen, whereas four were achieved using cryopreserved semen. These data provide new information on female bottlenose dolphin reproductive physiology, and demonstrate that the combination of endocrine monitoring and serial ultrasonography contributed to successful AI using liquid-stored and cryopreserved semen. |
doi_str_mv | 10.1530/rep.1.00516 |
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Specific objectives were: (i) to determine the excretory dynamics of urinary luteinizing hormone (LH) and ovarian steroid metabolites during the estrous cycle; (ii) to evaluate the effect of an exogenously administered synthetic progesterone analog (altrenogest) on reproductive hormone excretion; (iii) to correlate follicular growth and ovulation (as determined by transabdominal ultrasound) to urinary LH and ovarian steroid metabolites; (iv) examine the in vivo fertilisation capacity of cryopreserved semen, and (v) to develop an intrauterine insemination technique. Based on urinary endocrine monitoring of natural estrous cycles (2 consecutive cycles) and nine post altrenogest cycles in ten females, estrous cycles were found to be 36 days long and comprised of an 8 day and 19 day follicular and luteal phase, respectively. Peak estrogen conjugates (EC; 5.4 ± 3.8 ng/mg creatinine (Cr)) occurred 8 h prior to the LH surge (70.9 ± 115.7 ng/mg Cr). The time of ovulation, as determined by ultrasonography, occurred 32.1 ± 8.9 h and 24.3 ± 7.0 h after the onset of the LH surge and LH peak, respectively. Mean preovulatory follicular diameter and circumference were 2.1 ± 0.5 cm and 6.5 ± 1.5 cm, respectively. Of the 27 estrous synchronisation attempts, 13 resulted in an ovulatory cycle, with ovulation occurring 21 days post-altrenogest treatment. Intrauterine (4 of 5) and intracornual (1 of 3) inseminations conducted across eight estrous cycles resulted in five pregnancies (63%), one pregnancy resulted from the use of liquid stored semen, whereas four were achieved using cryopreserved semen. These data provide new information on female bottlenose dolphin reproductive physiology, and demonstrate that the combination of endocrine monitoring and serial ultrasonography contributed to successful AI using liquid-stored and cryopreserved semen.</description><identifier>ISSN: 1470-1626</identifier><identifier>EISSN: 1741-7899</identifier><identifier>DOI: 10.1530/rep.1.00516</identifier><identifier>PMID: 15855629</identifier><language>eng</language><publisher>Colchester: Society for Reproduction and Fertility</publisher><subject>acrosome ; Animals ; anovulation ; artificial insemination ; Biological and medical sciences ; Cryopreservation ; dolphins ; Dolphins - physiology ; Estrogens - urine ; estrous cycle ; Estrous Cycle - physiology ; Estrus Detection - methods ; Estrus Synchronization - methods ; Female ; follicular atresia ; Fundamental and applied biological sciences. Psychology ; Insemination, Artificial - methods ; Insemination, Artificial - veterinary ; luteinizing hormone ; Luteinizing Hormone - urine ; Male ; Mammalian male genital system ; Morphology. Physiology ; Ovary - diagnostic imaging ; ovulation ; polyspermy ; Pregnancy ; Progesterone - urine ; Progesterone Congeners - pharmacology ; Semen Preservation - methods ; Semen Preservation - veterinary ; synthetic progestogens ; Trenbolone Acetate - analogs & derivatives ; Trenbolone Acetate - pharmacology ; Tursiops truncatus ; Ultrasonography ; urine ; Vertebrates: reproduction</subject><ispartof>Reproduction (Cambridge, England), 2005-05, Vol.129 (5), p.659-674</ispartof><rights>2005 Society for Reproduction and Fertility</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b526t-1dba1869f45d60841cdc50d3ece2d9b84e90e4a6bad8aa12bad459f9e641ff683</citedby><cites>FETCH-LOGICAL-b526t-1dba1869f45d60841cdc50d3ece2d9b84e90e4a6bad8aa12bad459f9e641ff683</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16768994$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15855629$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Robeck, TR</creatorcontrib><creatorcontrib>Steinman, KJ</creatorcontrib><creatorcontrib>Yoshioka, M</creatorcontrib><creatorcontrib>Jensen, E</creatorcontrib><creatorcontrib>O’Brien, JK</creatorcontrib><creatorcontrib>Katsumata, E</creatorcontrib><creatorcontrib>Gili, C</creatorcontrib><creatorcontrib>McBain, JF</creatorcontrib><creatorcontrib>Sweeney, J</creatorcontrib><creatorcontrib>Monfort, SL</creatorcontrib><title>Estrous cycle characterisation and artificial insemination using frozen–thawed spermatozoa in the bottlenose dolphin (Tursiops truncatus)</title><title>Reproduction (Cambridge, England)</title><addtitle>Reproduction</addtitle><description>The reproductive endocrinology of the bottlenose dolphin, Tursiops truncatus, was characterized to facilitate the development of artificial insemination using cryopreserved spermatozoa. Specific objectives were: (i) to determine the excretory dynamics of urinary luteinizing hormone (LH) and ovarian steroid metabolites during the estrous cycle; (ii) to evaluate the effect of an exogenously administered synthetic progesterone analog (altrenogest) on reproductive hormone excretion; (iii) to correlate follicular growth and ovulation (as determined by transabdominal ultrasound) to urinary LH and ovarian steroid metabolites; (iv) examine the in vivo fertilisation capacity of cryopreserved semen, and (v) to develop an intrauterine insemination technique. Based on urinary endocrine monitoring of natural estrous cycles (2 consecutive cycles) and nine post altrenogest cycles in ten females, estrous cycles were found to be 36 days long and comprised of an 8 day and 19 day follicular and luteal phase, respectively. Peak estrogen conjugates (EC; 5.4 ± 3.8 ng/mg creatinine (Cr)) occurred 8 h prior to the LH surge (70.9 ± 115.7 ng/mg Cr). The time of ovulation, as determined by ultrasonography, occurred 32.1 ± 8.9 h and 24.3 ± 7.0 h after the onset of the LH surge and LH peak, respectively. Mean preovulatory follicular diameter and circumference were 2.1 ± 0.5 cm and 6.5 ± 1.5 cm, respectively. Of the 27 estrous synchronisation attempts, 13 resulted in an ovulatory cycle, with ovulation occurring 21 days post-altrenogest treatment. Intrauterine (4 of 5) and intracornual (1 of 3) inseminations conducted across eight estrous cycles resulted in five pregnancies (63%), one pregnancy resulted from the use of liquid stored semen, whereas four were achieved using cryopreserved semen. These data provide new information on female bottlenose dolphin reproductive physiology, and demonstrate that the combination of endocrine monitoring and serial ultrasonography contributed to successful AI using liquid-stored and cryopreserved semen.</description><subject>acrosome</subject><subject>Animals</subject><subject>anovulation</subject><subject>artificial insemination</subject><subject>Biological and medical sciences</subject><subject>Cryopreservation</subject><subject>dolphins</subject><subject>Dolphins - physiology</subject><subject>Estrogens - urine</subject><subject>estrous cycle</subject><subject>Estrous Cycle - physiology</subject><subject>Estrus Detection - methods</subject><subject>Estrus Synchronization - methods</subject><subject>Female</subject><subject>follicular atresia</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Insemination, Artificial - methods</subject><subject>Insemination, Artificial - veterinary</subject><subject>luteinizing hormone</subject><subject>Luteinizing Hormone - urine</subject><subject>Male</subject><subject>Mammalian male genital system</subject><subject>Morphology. Physiology</subject><subject>Ovary - diagnostic imaging</subject><subject>ovulation</subject><subject>polyspermy</subject><subject>Pregnancy</subject><subject>Progesterone - urine</subject><subject>Progesterone Congeners - pharmacology</subject><subject>Semen Preservation - methods</subject><subject>Semen Preservation - veterinary</subject><subject>synthetic progestogens</subject><subject>Trenbolone Acetate - analogs & derivatives</subject><subject>Trenbolone Acetate - pharmacology</subject><subject>Tursiops truncatus</subject><subject>Ultrasonography</subject><subject>urine</subject><subject>Vertebrates: reproduction</subject><issn>1470-1626</issn><issn>1741-7899</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU2L1TAUhosozji6cq_ZKIr0mrRN2i5lGD9gwIUz63CanNxGepOapAwzK_cu_Yf-EnOnFwYEdfWG5Ml5SZ6ieMrohvGavg04b9iGUs7EveKYtQ0r267v7-d109KSiUocFY9i_Eop410rHhZHOTkXVX9c_DiLKfglEnWtJiRqhAAqYbARkvWOgNMEQrLGKgsTsS7izrr1bInWbYkJ_gbdr-8_0whXqEmcMewg-RsPGSdpRDL4lCZ0PiLRfprHvP3qYgnR-jmSFBanIC3x9ePigYEp4pNDnhSX788uTj-W558_fDp9d14OvBKpZHoA1oneNFwL2jVMacWprlFhpfuha7Cn2IAYQHcArMrZ8N70KBpmjOjqk-LlOncO_tuCMcmdjQqnCRzmr5CibbtOtPy_IGtrXvGqyeCbFVTBxxjQyDnYHYRryajcS5JZkmTyVlKmnx3GLsMO9R17sJKBFwcAooLJBHDKxjtOtCIL3tdWKzfa7XhlA8rB-qgsulth8Jf25-slA17CNpuWl18qympK-75txL6ercQf0_71pt_z08qw</recordid><startdate>20050501</startdate><enddate>20050501</enddate><creator>Robeck, TR</creator><creator>Steinman, KJ</creator><creator>Yoshioka, M</creator><creator>Jensen, E</creator><creator>O’Brien, JK</creator><creator>Katsumata, E</creator><creator>Gili, C</creator><creator>McBain, JF</creator><creator>Sweeney, J</creator><creator>Monfort, SL</creator><general>Society for Reproduction and Fertility</general><general>Portland</general><scope>FBQ</scope><scope>IQODW</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>F1W</scope><scope>H95</scope><scope>L.G</scope><scope>7X8</scope></search><sort><creationdate>20050501</creationdate><title>Estrous cycle characterisation and artificial insemination using frozen–thawed spermatozoa in the bottlenose dolphin (Tursiops truncatus)</title><author>Robeck, TR ; Steinman, KJ ; Yoshioka, M ; Jensen, E ; O’Brien, JK ; Katsumata, E ; Gili, C ; McBain, JF ; Sweeney, J ; Monfort, SL</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b526t-1dba1869f45d60841cdc50d3ece2d9b84e90e4a6bad8aa12bad459f9e641ff683</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>acrosome</topic><topic>Animals</topic><topic>anovulation</topic><topic>artificial insemination</topic><topic>Biological and medical sciences</topic><topic>Cryopreservation</topic><topic>dolphins</topic><topic>Dolphins - physiology</topic><topic>Estrogens - urine</topic><topic>estrous cycle</topic><topic>Estrous Cycle - physiology</topic><topic>Estrus Detection - methods</topic><topic>Estrus Synchronization - methods</topic><topic>Female</topic><topic>follicular atresia</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Insemination, Artificial - methods</topic><topic>Insemination, Artificial - veterinary</topic><topic>luteinizing hormone</topic><topic>Luteinizing Hormone - urine</topic><topic>Male</topic><topic>Mammalian male genital system</topic><topic>Morphology. Physiology</topic><topic>Ovary - diagnostic imaging</topic><topic>ovulation</topic><topic>polyspermy</topic><topic>Pregnancy</topic><topic>Progesterone - urine</topic><topic>Progesterone Congeners - pharmacology</topic><topic>Semen Preservation - methods</topic><topic>Semen Preservation - veterinary</topic><topic>synthetic progestogens</topic><topic>Trenbolone Acetate - analogs & derivatives</topic><topic>Trenbolone Acetate - pharmacology</topic><topic>Tursiops truncatus</topic><topic>Ultrasonography</topic><topic>urine</topic><topic>Vertebrates: reproduction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Robeck, TR</creatorcontrib><creatorcontrib>Steinman, KJ</creatorcontrib><creatorcontrib>Yoshioka, M</creatorcontrib><creatorcontrib>Jensen, E</creatorcontrib><creatorcontrib>O’Brien, JK</creatorcontrib><creatorcontrib>Katsumata, E</creatorcontrib><creatorcontrib>Gili, C</creatorcontrib><creatorcontrib>McBain, JF</creatorcontrib><creatorcontrib>Sweeney, J</creatorcontrib><creatorcontrib>Monfort, SL</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>MEDLINE - Academic</collection><jtitle>Reproduction (Cambridge, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Robeck, TR</au><au>Steinman, KJ</au><au>Yoshioka, M</au><au>Jensen, E</au><au>O’Brien, JK</au><au>Katsumata, E</au><au>Gili, C</au><au>McBain, JF</au><au>Sweeney, J</au><au>Monfort, SL</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Estrous cycle characterisation and artificial insemination using frozen–thawed spermatozoa in the bottlenose dolphin (Tursiops truncatus)</atitle><jtitle>Reproduction (Cambridge, England)</jtitle><addtitle>Reproduction</addtitle><date>2005-05-01</date><risdate>2005</risdate><volume>129</volume><issue>5</issue><spage>659</spage><epage>674</epage><pages>659-674</pages><issn>1470-1626</issn><eissn>1741-7899</eissn><abstract>The reproductive endocrinology of the bottlenose dolphin, Tursiops truncatus, was characterized to facilitate the development of artificial insemination using cryopreserved spermatozoa. Specific objectives were: (i) to determine the excretory dynamics of urinary luteinizing hormone (LH) and ovarian steroid metabolites during the estrous cycle; (ii) to evaluate the effect of an exogenously administered synthetic progesterone analog (altrenogest) on reproductive hormone excretion; (iii) to correlate follicular growth and ovulation (as determined by transabdominal ultrasound) to urinary LH and ovarian steroid metabolites; (iv) examine the in vivo fertilisation capacity of cryopreserved semen, and (v) to develop an intrauterine insemination technique. Based on urinary endocrine monitoring of natural estrous cycles (2 consecutive cycles) and nine post altrenogest cycles in ten females, estrous cycles were found to be 36 days long and comprised of an 8 day and 19 day follicular and luteal phase, respectively. Peak estrogen conjugates (EC; 5.4 ± 3.8 ng/mg creatinine (Cr)) occurred 8 h prior to the LH surge (70.9 ± 115.7 ng/mg Cr). The time of ovulation, as determined by ultrasonography, occurred 32.1 ± 8.9 h and 24.3 ± 7.0 h after the onset of the LH surge and LH peak, respectively. Mean preovulatory follicular diameter and circumference were 2.1 ± 0.5 cm and 6.5 ± 1.5 cm, respectively. Of the 27 estrous synchronisation attempts, 13 resulted in an ovulatory cycle, with ovulation occurring 21 days post-altrenogest treatment. Intrauterine (4 of 5) and intracornual (1 of 3) inseminations conducted across eight estrous cycles resulted in five pregnancies (63%), one pregnancy resulted from the use of liquid stored semen, whereas four were achieved using cryopreserved semen. These data provide new information on female bottlenose dolphin reproductive physiology, and demonstrate that the combination of endocrine monitoring and serial ultrasonography contributed to successful AI using liquid-stored and cryopreserved semen.</abstract><cop>Colchester</cop><pub>Society for Reproduction and Fertility</pub><pmid>15855629</pmid><doi>10.1530/rep.1.00516</doi><tpages>16</tpages><oa>free_for_read</oa></addata></record> |
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subjects | acrosome Animals anovulation artificial insemination Biological and medical sciences Cryopreservation dolphins Dolphins - physiology Estrogens - urine estrous cycle Estrous Cycle - physiology Estrus Detection - methods Estrus Synchronization - methods Female follicular atresia Fundamental and applied biological sciences. Psychology Insemination, Artificial - methods Insemination, Artificial - veterinary luteinizing hormone Luteinizing Hormone - urine Male Mammalian male genital system Morphology. Physiology Ovary - diagnostic imaging ovulation polyspermy Pregnancy Progesterone - urine Progesterone Congeners - pharmacology Semen Preservation - methods Semen Preservation - veterinary synthetic progestogens Trenbolone Acetate - analogs & derivatives Trenbolone Acetate - pharmacology Tursiops truncatus Ultrasonography urine Vertebrates: reproduction |
title | Estrous cycle characterisation and artificial insemination using frozen–thawed spermatozoa in the bottlenose dolphin (Tursiops truncatus) |
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