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
Hauptverfasser: You, Jinyoung, Kim, Jinyoung, Lim, Jeongmook, Lee, Eunsong
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container_title Theriogenology
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creator You, Jinyoung
Kim, Jinyoung
Lim, Jeongmook
Lee, Eunsong
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
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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 &lt; 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 &lt; 0.05) expression of DNMT1, PCNA, FGFR2, and POU5F1 mRNA compared to control embryos. 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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; 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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 &lt; 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 &lt; 0.05) expression of DNMT1, PCNA, FGFR2, and POU5F1 mRNA compared to control embryos. 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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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