First pregnancy after in vitro culture of early antral follicles in goats: Positive effects of anethole on follicle development and steroidogenesis

This study aimed to evaluate the role of anethole during the in vitro culture of caprine early antral follicles. Early antral follicles were isolated from caprine ovaries and cultured for 18 days without (control) or with anethole (300 µg/ml). After culture, the cumulus–oocyte complexes were subject...

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Veröffentlicht in:Molecular reproduction and development 2020-09, Vol.87 (9), p.966-977
Hauptverfasser: Sá, Naiza A. R., Ferreira, Anna C. A., Sousa, Francisca G. C., Duarte, Ana B. G., Paes, Victor. M., Cadenas, Jesús, Anjos, Jefferson C., Fernandes, César C. L., Rosseto, Rafael, Cibin, Francielli W. S., Alves, Benner G., Rodrigues, Ana P. R., Rondina, David, Gastal, Eduardo L., Figueiredo, José R.
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container_end_page 977
container_issue 9
container_start_page 966
container_title Molecular reproduction and development
container_volume 87
creator Sá, Naiza A. R.
Ferreira, Anna C. A.
Sousa, Francisca G. C.
Duarte, Ana B. G.
Paes, Victor. M.
Cadenas, Jesús
Anjos, Jefferson C.
Fernandes, César C. L.
Rosseto, Rafael
Cibin, Francielli W. S.
Alves, Benner G.
Rodrigues, Ana P. R.
Rondina, David
Gastal, Eduardo L.
Figueiredo, José R.
description This study aimed to evaluate the role of anethole during the in vitro culture of caprine early antral follicles. Early antral follicles were isolated from caprine ovaries and cultured for 18 days without (control) or with anethole (300 µg/ml). After culture, the cumulus–oocyte complexes were subjected to in vitro maturation, followed by parthenogenetic activation or in vitro fertilization (IVF) and embryo culture. Follicular walls were used for the quantification of messenger RNA (mRNA) of CYP19A1, CYP17, MMP‐9, TIMP‐2, Bax, and Bcl‐2 genes, and culture medium was used for evaluation of ferric reducing antioxidant power (FRAP) and estradiol levels. After in vitro follicle culture (IVFC), anethole induced higher total antioxidant capacity, that is, it produced higher FRAP levels, reduced the Bax/Bcl‐2 ratio, and increased the levels of mRNA for CYP19A1 and CYP17, which was associated with a greater estradiol production (p 
doi_str_mv 10.1002/mrd.23410
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R. ; Ferreira, Anna C. A. ; Sousa, Francisca G. C. ; Duarte, Ana B. G. ; Paes, Victor. M. ; Cadenas, Jesús ; Anjos, Jefferson C. ; Fernandes, César C. L. ; Rosseto, Rafael ; Cibin, Francielli W. S. ; Alves, Benner G. ; Rodrigues, Ana P. R. ; Rondina, David ; Gastal, Eduardo L. ; Figueiredo, José R.</creator><creatorcontrib>Sá, Naiza A. R. ; Ferreira, Anna C. A. ; Sousa, Francisca G. C. ; Duarte, Ana B. G. ; Paes, Victor. M. ; Cadenas, Jesús ; Anjos, Jefferson C. ; Fernandes, César C. L. ; Rosseto, Rafael ; Cibin, Francielli W. S. ; Alves, Benner G. ; Rodrigues, Ana P. R. ; Rondina, David ; Gastal, Eduardo L. ; Figueiredo, José R.</creatorcontrib><description>This study aimed to evaluate the role of anethole during the in vitro culture of caprine early antral follicles. Early antral follicles were isolated from caprine ovaries and cultured for 18 days without (control) or with anethole (300 µg/ml). After culture, the cumulus–oocyte complexes were subjected to in vitro maturation, followed by parthenogenetic activation or in vitro fertilization (IVF) and embryo culture. Follicular walls were used for the quantification of messenger RNA (mRNA) of CYP19A1, CYP17, MMP‐9, TIMP‐2, Bax, and Bcl‐2 genes, and culture medium was used for evaluation of ferric reducing antioxidant power (FRAP) and estradiol levels. After in vitro follicle culture (IVFC), anethole induced higher total antioxidant capacity, that is, it produced higher FRAP levels, reduced the Bax/Bcl‐2 ratio, and increased the levels of mRNA for CYP19A1 and CYP17, which was associated with a greater estradiol production (p &lt; .05). Also, anethole improved the ability of oocytes to resume meiosis and reach metaphase II stage, as well as yielded higher (p &lt; .05) embryo production (e.g., morulas and blastocysts) in both parthenogenetic activation and IVF techniques. One pregnancy (Day 30) was obtained from IVFC with anethole. In conclusion, anethole promoted in vitro growth and maturation of goat early antral follicles and oocytes and enabled embryo production. Furthermore, this study reports, for the first time in goats, a pregnancy after IVF using oocytes originated from early antral follicles grown in vitro. This study reports for the first time in goats a pregnancy after in vitro fertilization using oocytes originated from early antral follicles grown in vitro. Isolated early antral follicles were cultured in a medium containing anethole. Anethole positively affected oocyte maturation and embryo development, as well as increased the total antioxidant capacity and downregulated the expression of proapoptotic genes.</description><identifier>ISSN: 1040-452X</identifier><identifier>EISSN: 1098-2795</identifier><identifier>DOI: 10.1002/mrd.23410</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc</publisher><subject>17β-Estradiol ; Anethole ; Antioxidants ; antral follicle ; Blastocysts ; Follicles ; FRAP ; goat ; In vitro fertilization ; Meiosis ; Metaphase ; mRNA ; oocyte and embryo ; Oocytes ; Ovaries ; Pregnancy ; Steroidogenesis ; Tissue inhibitor of metalloproteinases</subject><ispartof>Molecular reproduction and development, 2020-09, Vol.87 (9), p.966-977</ispartof><rights>2020 Wiley Periodicals LLC</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3300-f6ff26d045bae3535426accb00a387da3152fd4e455e7d0d284f6b0457f5eb8f3</citedby><cites>FETCH-LOGICAL-c3300-f6ff26d045bae3535426accb00a387da3152fd4e455e7d0d284f6b0457f5eb8f3</cites><orcidid>0000-0003-4745-0108 ; 0000-0002-8855-6980 ; 0000-0002-5139-0964</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fmrd.23410$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fmrd.23410$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,27926,27927,45576,45577</link.rule.ids></links><search><creatorcontrib>Sá, Naiza A. R.</creatorcontrib><creatorcontrib>Ferreira, Anna C. A.</creatorcontrib><creatorcontrib>Sousa, Francisca G. C.</creatorcontrib><creatorcontrib>Duarte, Ana B. G.</creatorcontrib><creatorcontrib>Paes, Victor. M.</creatorcontrib><creatorcontrib>Cadenas, Jesús</creatorcontrib><creatorcontrib>Anjos, Jefferson C.</creatorcontrib><creatorcontrib>Fernandes, César C. L.</creatorcontrib><creatorcontrib>Rosseto, Rafael</creatorcontrib><creatorcontrib>Cibin, Francielli W. S.</creatorcontrib><creatorcontrib>Alves, Benner G.</creatorcontrib><creatorcontrib>Rodrigues, Ana P. R.</creatorcontrib><creatorcontrib>Rondina, David</creatorcontrib><creatorcontrib>Gastal, Eduardo L.</creatorcontrib><creatorcontrib>Figueiredo, José R.</creatorcontrib><title>First pregnancy after in vitro culture of early antral follicles in goats: Positive effects of anethole on follicle development and steroidogenesis</title><title>Molecular reproduction and development</title><description>This study aimed to evaluate the role of anethole during the in vitro culture of caprine early antral follicles. Early antral follicles were isolated from caprine ovaries and cultured for 18 days without (control) or with anethole (300 µg/ml). After culture, the cumulus–oocyte complexes were subjected to in vitro maturation, followed by parthenogenetic activation or in vitro fertilization (IVF) and embryo culture. Follicular walls were used for the quantification of messenger RNA (mRNA) of CYP19A1, CYP17, MMP‐9, TIMP‐2, Bax, and Bcl‐2 genes, and culture medium was used for evaluation of ferric reducing antioxidant power (FRAP) and estradiol levels. After in vitro follicle culture (IVFC), anethole induced higher total antioxidant capacity, that is, it produced higher FRAP levels, reduced the Bax/Bcl‐2 ratio, and increased the levels of mRNA for CYP19A1 and CYP17, which was associated with a greater estradiol production (p &lt; .05). Also, anethole improved the ability of oocytes to resume meiosis and reach metaphase II stage, as well as yielded higher (p &lt; .05) embryo production (e.g., morulas and blastocysts) in both parthenogenetic activation and IVF techniques. One pregnancy (Day 30) was obtained from IVFC with anethole. In conclusion, anethole promoted in vitro growth and maturation of goat early antral follicles and oocytes and enabled embryo production. 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R.</creatorcontrib><creatorcontrib>Rondina, David</creatorcontrib><creatorcontrib>Gastal, Eduardo L.</creatorcontrib><creatorcontrib>Figueiredo, José R.</creatorcontrib><collection>CrossRef</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular reproduction and development</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sá, Naiza A. R.</au><au>Ferreira, Anna C. A.</au><au>Sousa, Francisca G. C.</au><au>Duarte, Ana B. G.</au><au>Paes, Victor. M.</au><au>Cadenas, Jesús</au><au>Anjos, Jefferson C.</au><au>Fernandes, César C. L.</au><au>Rosseto, Rafael</au><au>Cibin, Francielli W. S.</au><au>Alves, Benner G.</au><au>Rodrigues, Ana P. R.</au><au>Rondina, David</au><au>Gastal, Eduardo L.</au><au>Figueiredo, José R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>First pregnancy after in vitro culture of early antral follicles in goats: Positive effects of anethole on follicle development and steroidogenesis</atitle><jtitle>Molecular reproduction and development</jtitle><date>2020-09</date><risdate>2020</risdate><volume>87</volume><issue>9</issue><spage>966</spage><epage>977</epage><pages>966-977</pages><issn>1040-452X</issn><eissn>1098-2795</eissn><abstract>This study aimed to evaluate the role of anethole during the in vitro culture of caprine early antral follicles. Early antral follicles were isolated from caprine ovaries and cultured for 18 days without (control) or with anethole (300 µg/ml). After culture, the cumulus–oocyte complexes were subjected to in vitro maturation, followed by parthenogenetic activation or in vitro fertilization (IVF) and embryo culture. Follicular walls were used for the quantification of messenger RNA (mRNA) of CYP19A1, CYP17, MMP‐9, TIMP‐2, Bax, and Bcl‐2 genes, and culture medium was used for evaluation of ferric reducing antioxidant power (FRAP) and estradiol levels. After in vitro follicle culture (IVFC), anethole induced higher total antioxidant capacity, that is, it produced higher FRAP levels, reduced the Bax/Bcl‐2 ratio, and increased the levels of mRNA for CYP19A1 and CYP17, which was associated with a greater estradiol production (p &lt; .05). Also, anethole improved the ability of oocytes to resume meiosis and reach metaphase II stage, as well as yielded higher (p &lt; .05) embryo production (e.g., morulas and blastocysts) in both parthenogenetic activation and IVF techniques. One pregnancy (Day 30) was obtained from IVFC with anethole. In conclusion, anethole promoted in vitro growth and maturation of goat early antral follicles and oocytes and enabled embryo production. Furthermore, this study reports, for the first time in goats, a pregnancy after IVF using oocytes originated from early antral follicles grown in vitro. This study reports for the first time in goats a pregnancy after in vitro fertilization using oocytes originated from early antral follicles grown in vitro. Isolated early antral follicles were cultured in a medium containing anethole. Anethole positively affected oocyte maturation and embryo development, as well as increased the total antioxidant capacity and downregulated the expression of proapoptotic genes.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/mrd.23410</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0003-4745-0108</orcidid><orcidid>https://orcid.org/0000-0002-8855-6980</orcidid><orcidid>https://orcid.org/0000-0002-5139-0964</orcidid></addata></record>
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subjects 17β-Estradiol
Anethole
Antioxidants
antral follicle
Blastocysts
Follicles
FRAP
goat
In vitro fertilization
Meiosis
Metaphase
mRNA
oocyte and embryo
Oocytes
Ovaries
Pregnancy
Steroidogenesis
Tissue inhibitor of metalloproteinases
title First pregnancy after in vitro culture of early antral follicles in goats: Positive effects of anethole on follicle development and steroidogenesis
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