Supplementation of lycopene in maturation media improves bovine embryo quality in vitro

This study sought to modulate factors that reduce embryo quality in in vitro culture (IVC) systems. Over eight replicates, 3075 oocytes were cultured in in vitro maturation media containing various concentrations of lycopene, followed by in vitro fertilization and culture. The percentages of MII-sta...

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Veröffentlicht in:Theriogenology 2017-11, Vol.103, p.173-184
Hauptverfasser: Chowdhury, M.M.R., Choi, Byung-Hyun, Khan, Imran, Lee, Kyeong-Lim, Mesalam, Ayman, Song, Seok-Hwan, Xu, Lianguang, Joo, Myeong-Don, Afrin, Fahmida, Kong, Il-Keun
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container_start_page 173
container_title Theriogenology
container_volume 103
creator Chowdhury, M.M.R.
Choi, Byung-Hyun
Khan, Imran
Lee, Kyeong-Lim
Mesalam, Ayman
Song, Seok-Hwan
Xu, Lianguang
Joo, Myeong-Don
Afrin, Fahmida
Kong, Il-Keun
description This study sought to modulate factors that reduce embryo quality in in vitro culture (IVC) systems. Over eight replicates, 3075 oocytes were cultured in in vitro maturation media containing various concentrations of lycopene, followed by in vitro fertilization and culture. The percentages of MII-stage oocytes, the presumptive zygotes that underwent cleavage and developed into blastocysts were significantly (P 
doi_str_mv 10.1016/j.theriogenology.2017.08.003
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Over eight replicates, 3075 oocytes were cultured in in vitro maturation media containing various concentrations of lycopene, followed by in vitro fertilization and culture. The percentages of MII-stage oocytes, the presumptive zygotes that underwent cleavage and developed into blastocysts were significantly (P &lt; 0.05) higher, the intracellular ROS concentrations reduced significantly (P &lt; 0.05) in oocytes/blastocysts, TUNEL assay demonstrates reduced apoptosis and increased total cell number per blastocyst (P &lt; 0.05), Immunocytochemistry confirmed that diminished protein expression of nuclear factor kappa B (NFκB), cyclooxygenase-2 (COX2), and 8-oxoguanine (indicated by ROS) and relative mRNA expression of the Caspase-3, NFκB, COX2, iNOS and BCL2-associated X (BAX) was significantly (P &lt; 0.05) lower whereas the anti-apoptotic gene BCL2 was significantly (P &lt; 0.05) higher in the 0.2 μM lycopene-supplemented group than the control. In conclusion, lycopene improves blastocyst quality by overcoming unfavorable conditions in in vitro culture systems.</description><identifier>ISSN: 0093-691X</identifier><identifier>EISSN: 1879-3231</identifier><identifier>DOI: 10.1016/j.theriogenology.2017.08.003</identifier><identifier>PMID: 28800556</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Apoptosis - drug effects ; Blastocyst - cytology ; Blastocyst - physiology ; Bovine ; Carotenoids - chemistry ; Carotenoids - pharmacology ; Cattle - embryology ; Culture Media ; Cumulus Cells ; Embryo culture ; Embryo Culture Techniques - veterinary ; Embryonic Development - drug effects ; Fertilization in Vitro ; Free radicals ; In Vitro Oocyte Maturation Techniques ; Lycopene ; Molecular Structure ; Oocytes - physiology ; Oxidative stress ; Reactive Oxygen Species ; RNA, Messenger</subject><ispartof>Theriogenology, 2017-11, Vol.103, p.173-184</ispartof><rights>2017 Elsevier Inc.</rights><rights>Copyright © 2017 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c386t-6a6d939db095a4e2349847f881625a7700df2c566f882741c8cbb6c9def51e0c3</citedby><cites>FETCH-LOGICAL-c386t-6a6d939db095a4e2349847f881625a7700df2c566f882741c8cbb6c9def51e0c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.theriogenology.2017.08.003$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28800556$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chowdhury, M.M.R.</creatorcontrib><creatorcontrib>Choi, Byung-Hyun</creatorcontrib><creatorcontrib>Khan, Imran</creatorcontrib><creatorcontrib>Lee, Kyeong-Lim</creatorcontrib><creatorcontrib>Mesalam, Ayman</creatorcontrib><creatorcontrib>Song, Seok-Hwan</creatorcontrib><creatorcontrib>Xu, Lianguang</creatorcontrib><creatorcontrib>Joo, Myeong-Don</creatorcontrib><creatorcontrib>Afrin, Fahmida</creatorcontrib><creatorcontrib>Kong, Il-Keun</creatorcontrib><title>Supplementation of lycopene in maturation media improves bovine embryo quality in vitro</title><title>Theriogenology</title><addtitle>Theriogenology</addtitle><description>This study sought to modulate factors that reduce embryo quality in in vitro culture (IVC) systems. Over eight replicates, 3075 oocytes were cultured in in vitro maturation media containing various concentrations of lycopene, followed by in vitro fertilization and culture. The percentages of MII-stage oocytes, the presumptive zygotes that underwent cleavage and developed into blastocysts were significantly (P &lt; 0.05) higher, the intracellular ROS concentrations reduced significantly (P &lt; 0.05) in oocytes/blastocysts, TUNEL assay demonstrates reduced apoptosis and increased total cell number per blastocyst (P &lt; 0.05), Immunocytochemistry confirmed that diminished protein expression of nuclear factor kappa B (NFκB), cyclooxygenase-2 (COX2), and 8-oxoguanine (indicated by ROS) and relative mRNA expression of the Caspase-3, NFκB, COX2, iNOS and BCL2-associated X (BAX) was significantly (P &lt; 0.05) lower whereas the anti-apoptotic gene BCL2 was significantly (P &lt; 0.05) higher in the 0.2 μM lycopene-supplemented group than the control. In conclusion, lycopene improves blastocyst quality by overcoming unfavorable conditions in in vitro culture systems.</description><subject>Animals</subject><subject>Apoptosis - drug effects</subject><subject>Blastocyst - cytology</subject><subject>Blastocyst - physiology</subject><subject>Bovine</subject><subject>Carotenoids - chemistry</subject><subject>Carotenoids - pharmacology</subject><subject>Cattle - embryology</subject><subject>Culture Media</subject><subject>Cumulus Cells</subject><subject>Embryo culture</subject><subject>Embryo Culture Techniques - veterinary</subject><subject>Embryonic Development - drug effects</subject><subject>Fertilization in Vitro</subject><subject>Free radicals</subject><subject>In Vitro Oocyte Maturation Techniques</subject><subject>Lycopene</subject><subject>Molecular Structure</subject><subject>Oocytes - physiology</subject><subject>Oxidative stress</subject><subject>Reactive Oxygen Species</subject><subject>RNA, Messenger</subject><issn>0093-691X</issn><issn>1879-3231</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkMtq3TAQhkVpaE7SvkLxIotu7IwsW5agmxByg0AXSSE7IcvjVAfbciT5gN8mz5Ini8JJC9l1JRh9_1w-Qk4oFBQoP90W8Q966x5xcoN7XIsSaFOAKADYJ7KhopE5Kxn9TDYAkuVc0odDchTCFhLBOf1CDkshAOqab8jD3TLPA444RR2tmzLXZ8Nq3IwTZnbKRh0Xv_8ZsbM6s-Ps3Q5D1rqdTQyOrV9d9rTowcY1RV6edzZ695Uc9HoI-O39PSa_Ly_uz6_z219XN-dnt7lhgseca95JJrsWZK0rLFklRdX0QlBe1rppALq-NDXnqVQ2FTXCtC03ssO-pgiGHZMf-75pracFQ1SjDQaHQU_olqCoLEVNGat4Qn_uUeNdCB57NXs7ar8qCurNrdqqj27Vm1sFQiVzKf79fdLSJhf_wn9lJuByD2C6d2fRq2AsTiZ582ii6pz9v0mvqYuWZQ</recordid><startdate>201711</startdate><enddate>201711</enddate><creator>Chowdhury, M.M.R.</creator><creator>Choi, Byung-Hyun</creator><creator>Khan, Imran</creator><creator>Lee, Kyeong-Lim</creator><creator>Mesalam, Ayman</creator><creator>Song, Seok-Hwan</creator><creator>Xu, Lianguang</creator><creator>Joo, Myeong-Don</creator><creator>Afrin, Fahmida</creator><creator>Kong, Il-Keun</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>201711</creationdate><title>Supplementation of lycopene in maturation media improves bovine embryo quality in vitro</title><author>Chowdhury, M.M.R. ; 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subjects Animals
Apoptosis - drug effects
Blastocyst - cytology
Blastocyst - physiology
Bovine
Carotenoids - chemistry
Carotenoids - pharmacology
Cattle - embryology
Culture Media
Cumulus Cells
Embryo culture
Embryo Culture Techniques - veterinary
Embryonic Development - drug effects
Fertilization in Vitro
Free radicals
In Vitro Oocyte Maturation Techniques
Lycopene
Molecular Structure
Oocytes - physiology
Oxidative stress
Reactive Oxygen Species
RNA, Messenger
title Supplementation of lycopene in maturation media improves bovine embryo quality in vitro
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