Anthocyanin stimulates in vitro development of cloned pig embryos by increasing the intracellular glutathione level and inhibiting reactive oxygen species
The objective was to examine the nuclear maturation of oocytes, embryonic development after parthenogenetic activation (PA) and somatic cell nuclear transfer (SCNT), and gene expression in SCNT embryos in pigs ( Sus scrofa) when anthocyanin was added to oocytes during maturation and in vitro culture...
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Veröffentlicht in: | Theriogenology 2010-09, Vol.74 (5), p.777-785 |
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description | The objective was to examine the nuclear maturation of oocytes, embryonic development after parthenogenetic activation (PA) and somatic cell nuclear transfer (SCNT), and gene expression in SCNT embryos in pigs (
Sus scrofa) when anthocyanin was added to oocytes during maturation and
in vitro culture (IVC) of embryos. Immature oocytes were untreated or treated with 0.1 μg/mL anthocyanin during
in vitro maturation (IVM). Next, PA and SCNT embryos were produced from oocytes and cultured in medium supplemented with or without 0.1 μg/mL anthocyanin for 7 d. Anthocyanin treatment during IVM did not improve the nuclear maturation of oocytes, but significantly increased intracellular glutathione (GSH) levels and reduced reactive oxygen species (ROS). Oocytes treated with anthocyanin during IVM had higher (
P < 0.05) rates of blastocyst formation after PA (55.7 vs. 44.9 %) and SCNT (32.2 vs. 16.1%) compared to untreated oocytes. In PA and SCNT embryos, anthocyanin treatment during IVM or IVC significantly increased the intracellular GSH level, which led to the reduced ROS level. Somatic cell nuclear transfer embryos derived from anthocyanin-treated oocytes had increased (
P < 0.05) expression of DNMT1, PCNA, FGFR2, and POU5F1 mRNA compared to control embryos. In conclusion, anthocyanin treatment during IVM improved developmental competence of SCNT embryos, most likely by increasing intracellular GSH synthesis, reducing ROS level, and stimulating nuclear reprogramming via increased transcription factor expression. |
doi_str_mv | 10.1016/j.theriogenology.2010.04.002 |
format | Article |
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Sus scrofa) when anthocyanin was added to oocytes during maturation and
in vitro culture (IVC) of embryos. Immature oocytes were untreated or treated with 0.1 μg/mL anthocyanin during
in vitro maturation (IVM). Next, PA and SCNT embryos were produced from oocytes and cultured in medium supplemented with or without 0.1 μg/mL anthocyanin for 7 d. Anthocyanin treatment during IVM did not improve the nuclear maturation of oocytes, but significantly increased intracellular glutathione (GSH) levels and reduced reactive oxygen species (ROS). Oocytes treated with anthocyanin during IVM had higher (
P < 0.05) rates of blastocyst formation after PA (55.7 vs. 44.9 %) and SCNT (32.2 vs. 16.1%) compared to untreated oocytes. In PA and SCNT embryos, anthocyanin treatment during IVM or IVC significantly increased the intracellular GSH level, which led to the reduced ROS level. Somatic cell nuclear transfer embryos derived from anthocyanin-treated oocytes had increased (
P < 0.05) expression of DNMT1, PCNA, FGFR2, and POU5F1 mRNA compared to control embryos. In conclusion, anthocyanin treatment during IVM improved developmental competence of SCNT embryos, most likely by increasing intracellular GSH synthesis, reducing ROS level, and stimulating nuclear reprogramming via increased transcription factor expression.</description><identifier>ISSN: 0093-691X</identifier><identifier>EISSN: 1879-3231</identifier><identifier>DOI: 10.1016/j.theriogenology.2010.04.002</identifier><identifier>PMID: 20537699</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>additives ; Animals ; Anthocyanin ; anthocyanins ; Anthocyanins - pharmacology ; antioxidant activity ; blastocyst ; cloning (animals) ; Cloning, Organism - veterinary ; culture media ; developmental competence ; embryo (animal) ; embryo culture ; Embryo Culture Techniques - veterinary ; Embryo, Mammalian - drug effects ; embryogenesis ; Embryonic development ; Embryonic Development - drug effects ; glutathione ; Glutathione - metabolism ; in vitro culture ; nuclear reprogramming ; Nuclear Transfer Techniques - veterinary ; nuclear transplantation ; oocytes ; parthenogenesis ; Parthenogenesis - genetics ; parthenogenetic activation ; Pig ; Reactive oxygen species ; Reactive Oxygen Species - metabolism ; Somatic cell nuclear transfer ; somatic cells ; swine ; Swine - embryology ; transcription factors</subject><ispartof>Theriogenology, 2010-09, Vol.74 (5), p.777-785</ispartof><rights>2010 Elsevier Inc.</rights><rights>Copyright 2010 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c475t-347258380c88f5f15779a0069e74658176c321b690da2a14324c83f5f38a665d3</citedby><cites>FETCH-LOGICAL-c475t-347258380c88f5f15779a0069e74658176c321b690da2a14324c83f5f38a665d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0093691X10001925$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27903,27904,65309</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20537699$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>You, Jinyoung</creatorcontrib><creatorcontrib>Kim, Jinyoung</creatorcontrib><creatorcontrib>Lim, Jeongmook</creatorcontrib><creatorcontrib>Lee, Eunsong</creatorcontrib><title>Anthocyanin stimulates in vitro development of cloned pig embryos by increasing the intracellular glutathione level and inhibiting reactive oxygen species</title><title>Theriogenology</title><addtitle>Theriogenology</addtitle><description>The objective was to examine the nuclear maturation of oocytes, embryonic development after parthenogenetic activation (PA) and somatic cell nuclear transfer (SCNT), and gene expression in SCNT embryos in pigs (
Sus scrofa) when anthocyanin was added to oocytes during maturation and
in vitro culture (IVC) of embryos. Immature oocytes were untreated or treated with 0.1 μg/mL anthocyanin during
in vitro maturation (IVM). Next, PA and SCNT embryos were produced from oocytes and cultured in medium supplemented with or without 0.1 μg/mL anthocyanin for 7 d. Anthocyanin treatment during IVM did not improve the nuclear maturation of oocytes, but significantly increased intracellular glutathione (GSH) levels and reduced reactive oxygen species (ROS). Oocytes treated with anthocyanin during IVM had higher (
P < 0.05) rates of blastocyst formation after PA (55.7 vs. 44.9 %) and SCNT (32.2 vs. 16.1%) compared to untreated oocytes. In PA and SCNT embryos, anthocyanin treatment during IVM or IVC significantly increased the intracellular GSH level, which led to the reduced ROS level. Somatic cell nuclear transfer embryos derived from anthocyanin-treated oocytes had increased (
P < 0.05) expression of DNMT1, PCNA, FGFR2, and POU5F1 mRNA compared to control embryos. In conclusion, anthocyanin treatment during IVM improved developmental competence of SCNT embryos, most likely by increasing intracellular GSH synthesis, reducing ROS level, and stimulating nuclear reprogramming via increased transcription factor expression.</description><subject>additives</subject><subject>Animals</subject><subject>Anthocyanin</subject><subject>anthocyanins</subject><subject>Anthocyanins - pharmacology</subject><subject>antioxidant activity</subject><subject>blastocyst</subject><subject>cloning (animals)</subject><subject>Cloning, Organism - veterinary</subject><subject>culture media</subject><subject>developmental competence</subject><subject>embryo (animal)</subject><subject>embryo culture</subject><subject>Embryo Culture Techniques - veterinary</subject><subject>Embryo, Mammalian - drug effects</subject><subject>embryogenesis</subject><subject>Embryonic development</subject><subject>Embryonic Development - drug effects</subject><subject>glutathione</subject><subject>Glutathione - metabolism</subject><subject>in vitro culture</subject><subject>nuclear reprogramming</subject><subject>Nuclear Transfer Techniques - veterinary</subject><subject>nuclear transplantation</subject><subject>oocytes</subject><subject>parthenogenesis</subject><subject>Parthenogenesis - genetics</subject><subject>parthenogenetic activation</subject><subject>Pig</subject><subject>Reactive oxygen species</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>Somatic cell nuclear transfer</subject><subject>somatic cells</subject><subject>swine</subject><subject>Swine - embryology</subject><subject>transcription factors</subject><issn>0093-691X</issn><issn>1879-3231</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkUGL1TAUhYMoznP0L2gWgqs-b5o2bcDNMMw4woALHXAX0vS2L4-2qUn6mP4Vf60pbxTcuQqXfOfk5B5C3jPYM2Di43EfD-it63Fyg-vXfQ7pCoo9QP6M7FhdyYznnD0nOwDJMyHZjwvyKoQjAHAh2EtykUPJKyHljvy6muLBmVVPdqIh2nEZdMRA03Sy0Tva4gkHN484Reo6agY3YUtn21McG7-6QJs10cajDnbqaQqXxui1wWFIZp72wxJ1PNgkpMPmRvXUJuZgGxs3SZKaaE9I3eOafkXDjMZieE1edHoI-ObpvCQPtzffr--y-6-fv1xf3WemqMqY8aLKy5rXYOq6KztWVpXUAEJiVYiyZpUwPGeNkNDqXLOC54WpeSJ5rYUoW35JPpx9Z-9-LhiiGm3Y0usJ3RJUVUhgJUiRyE9n0ngXgsdOzd6O2q-KgdrKUUf1bzlqK0dBoVI5Sf726aGlGbH9K_7TRgLenYFOO6V7b4N6-JYcOLC6zksBibg9E5gWcrLoVUirmgy21qOJqnX2_7L8BtY1tjw</recordid><startdate>20100915</startdate><enddate>20100915</enddate><creator>You, Jinyoung</creator><creator>Kim, Jinyoung</creator><creator>Lim, Jeongmook</creator><creator>Lee, Eunsong</creator><general>Elsevier Inc</general><general>[Oxford]: Butterworth-Heinemann; [New York]: 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>20100915</creationdate><title>Anthocyanin stimulates in vitro development of cloned pig embryos by increasing the intracellular glutathione level and inhibiting reactive oxygen species</title><author>You, Jinyoung ; Kim, Jinyoung ; Lim, Jeongmook ; Lee, Eunsong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c475t-347258380c88f5f15779a0069e74658176c321b690da2a14324c83f5f38a665d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>additives</topic><topic>Animals</topic><topic>Anthocyanin</topic><topic>anthocyanins</topic><topic>Anthocyanins - pharmacology</topic><topic>antioxidant activity</topic><topic>blastocyst</topic><topic>cloning (animals)</topic><topic>Cloning, Organism - veterinary</topic><topic>culture media</topic><topic>developmental competence</topic><topic>embryo (animal)</topic><topic>embryo culture</topic><topic>Embryo Culture Techniques - veterinary</topic><topic>Embryo, Mammalian - drug effects</topic><topic>embryogenesis</topic><topic>Embryonic development</topic><topic>Embryonic Development - drug effects</topic><topic>glutathione</topic><topic>Glutathione - metabolism</topic><topic>in vitro culture</topic><topic>nuclear reprogramming</topic><topic>Nuclear Transfer Techniques - veterinary</topic><topic>nuclear transplantation</topic><topic>oocytes</topic><topic>parthenogenesis</topic><topic>Parthenogenesis - genetics</topic><topic>parthenogenetic activation</topic><topic>Pig</topic><topic>Reactive oxygen species</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>Somatic cell nuclear transfer</topic><topic>somatic cells</topic><topic>swine</topic><topic>Swine - embryology</topic><topic>transcription factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>You, Jinyoung</creatorcontrib><creatorcontrib>Kim, Jinyoung</creatorcontrib><creatorcontrib>Lim, Jeongmook</creatorcontrib><creatorcontrib>Lee, Eunsong</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>Theriogenology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>You, Jinyoung</au><au>Kim, Jinyoung</au><au>Lim, Jeongmook</au><au>Lee, Eunsong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Anthocyanin stimulates in vitro development of cloned pig embryos by increasing the intracellular glutathione level and inhibiting reactive oxygen species</atitle><jtitle>Theriogenology</jtitle><addtitle>Theriogenology</addtitle><date>2010-09-15</date><risdate>2010</risdate><volume>74</volume><issue>5</issue><spage>777</spage><epage>785</epage><pages>777-785</pages><issn>0093-691X</issn><eissn>1879-3231</eissn><abstract>The objective was to examine the nuclear maturation of oocytes, embryonic development after parthenogenetic activation (PA) and somatic cell nuclear transfer (SCNT), and gene expression in SCNT embryos in pigs (
Sus scrofa) when anthocyanin was added to oocytes during maturation and
in vitro culture (IVC) of embryos. Immature oocytes were untreated or treated with 0.1 μg/mL anthocyanin during
in vitro maturation (IVM). Next, PA and SCNT embryos were produced from oocytes and cultured in medium supplemented with or without 0.1 μg/mL anthocyanin for 7 d. Anthocyanin treatment during IVM did not improve the nuclear maturation of oocytes, but significantly increased intracellular glutathione (GSH) levels and reduced reactive oxygen species (ROS). Oocytes treated with anthocyanin during IVM had higher (
P < 0.05) rates of blastocyst formation after PA (55.7 vs. 44.9 %) and SCNT (32.2 vs. 16.1%) compared to untreated oocytes. In PA and SCNT embryos, anthocyanin treatment during IVM or IVC significantly increased the intracellular GSH level, which led to the reduced ROS level. Somatic cell nuclear transfer embryos derived from anthocyanin-treated oocytes had increased (
P < 0.05) expression of DNMT1, PCNA, FGFR2, and POU5F1 mRNA compared to control embryos. In conclusion, anthocyanin treatment during IVM improved developmental competence of SCNT embryos, most likely by increasing intracellular GSH synthesis, reducing ROS level, and stimulating nuclear reprogramming via increased transcription factor expression.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>20537699</pmid><doi>10.1016/j.theriogenology.2010.04.002</doi><tpages>9</tpages></addata></record> |
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subjects | additives Animals Anthocyanin anthocyanins Anthocyanins - pharmacology antioxidant activity blastocyst cloning (animals) Cloning, Organism - veterinary culture media developmental competence embryo (animal) embryo culture Embryo Culture Techniques - veterinary Embryo, Mammalian - drug effects embryogenesis Embryonic development Embryonic Development - drug effects glutathione Glutathione - metabolism in vitro culture nuclear reprogramming Nuclear Transfer Techniques - veterinary nuclear transplantation oocytes parthenogenesis Parthenogenesis - genetics parthenogenetic activation Pig Reactive oxygen species Reactive Oxygen Species - metabolism Somatic cell nuclear transfer somatic cells swine Swine - embryology transcription factors |
title | Anthocyanin stimulates in vitro development of cloned pig embryos by increasing the intracellular glutathione level and inhibiting reactive oxygen species |
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