Cryopreservation time does not decrease follicular viability in ovarian tissue frozen for fertility preservation
Autor(a) principal: | |
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Data de Publicação: | 2011 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Clinics |
Texto Completo: | https://www.revistas.usp.br/clinics/article/view/19334 |
Resumo: | OBJECTIVE: To determine the effect of storage duration on cryopreserved ovarian tissue using fresh and frozenthawed samples. METHODS: Seventeen fertile patients underwent an ovarian biopsy during elective laparoscopic tubal ligation. The tissue sample was divided into three parts: one part was processed fresh (FG), and two were slowly frozen, cryopreserved for 30 (G30) or 180 days (G180), thawed and analyzed. Follicular density, follicular viability, and steroidogenic capacity were assessed. RESULTS: We observed no differences between the groups in follicular density, which was assessed in hematoxylin and eosin-stained tissue sections. A heterogeneous follicular distribution was observed in the parenchyma, with a mean density of 361.3±255.4, 454.9±676.3, and 296.8±269.0 follicles/mm3 for FG, G30 and G180, respectively (p = 0.46). Follicular viability was greater in FG (93.4%) when compared with the cryopreserved tissues (70.8% for G30 (p |
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Clinics |
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Cryopreservation time does not decrease follicular viability in ovarian tissue frozen for fertility preservation Ovarian tissueCryopreservationTissue damageOvarian steroidogenesisTissue culture OBJECTIVE: To determine the effect of storage duration on cryopreserved ovarian tissue using fresh and frozenthawed samples. METHODS: Seventeen fertile patients underwent an ovarian biopsy during elective laparoscopic tubal ligation. The tissue sample was divided into three parts: one part was processed fresh (FG), and two were slowly frozen, cryopreserved for 30 (G30) or 180 days (G180), thawed and analyzed. Follicular density, follicular viability, and steroidogenic capacity were assessed. RESULTS: We observed no differences between the groups in follicular density, which was assessed in hematoxylin and eosin-stained tissue sections. A heterogeneous follicular distribution was observed in the parenchyma, with a mean density of 361.3±255.4, 454.9±676.3, and 296.8±269.0 follicles/mm3 for FG, G30 and G180, respectively (p = 0.46). Follicular viability was greater in FG (93.4%) when compared with the cryopreserved tissues (70.8% for G30 (pHospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo2011-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/clinics/article/view/1933410.1590/S1807-59322011001200015Clinics; Vol. 66 No. 12 (2011); 2093-2097 Clinics; v. 66 n. 12 (2011); 2093-2097 Clinics; Vol. 66 Núm. 12 (2011); 2093-2097 1980-53221807-5932reponame:Clinicsinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/clinics/article/view/19334/21397Campos, Jacira RibeiroRosa-e-Silva, Julio CesarCarvalho, Bruno RamalhoVireque, Alessandra AparecidaSilva-de-Sá, Marcos FelipeRosa-e-Silva, Ana Carolina Japur de Sáinfo:eu-repo/semantics/openAccess2012-05-23T16:34:41Zoai:revistas.usp.br:article/19334Revistahttps://www.revistas.usp.br/clinicsPUBhttps://www.revistas.usp.br/clinics/oai||clinics@hc.fm.usp.br1980-53221807-5932opendoar:2012-05-23T16:34:41Clinics - Universidade de São Paulo (USP)false |
dc.title.none.fl_str_mv |
Cryopreservation time does not decrease follicular viability in ovarian tissue frozen for fertility preservation |
title |
Cryopreservation time does not decrease follicular viability in ovarian tissue frozen for fertility preservation |
spellingShingle |
Cryopreservation time does not decrease follicular viability in ovarian tissue frozen for fertility preservation Campos, Jacira Ribeiro Ovarian tissue Cryopreservation Tissue damage Ovarian steroidogenesis Tissue culture |
title_short |
Cryopreservation time does not decrease follicular viability in ovarian tissue frozen for fertility preservation |
title_full |
Cryopreservation time does not decrease follicular viability in ovarian tissue frozen for fertility preservation |
title_fullStr |
Cryopreservation time does not decrease follicular viability in ovarian tissue frozen for fertility preservation |
title_full_unstemmed |
Cryopreservation time does not decrease follicular viability in ovarian tissue frozen for fertility preservation |
title_sort |
Cryopreservation time does not decrease follicular viability in ovarian tissue frozen for fertility preservation |
author |
Campos, Jacira Ribeiro |
author_facet |
Campos, Jacira Ribeiro Rosa-e-Silva, Julio Cesar Carvalho, Bruno Ramalho Vireque, Alessandra Aparecida Silva-de-Sá, Marcos Felipe Rosa-e-Silva, Ana Carolina Japur de Sá |
author_role |
author |
author2 |
Rosa-e-Silva, Julio Cesar Carvalho, Bruno Ramalho Vireque, Alessandra Aparecida Silva-de-Sá, Marcos Felipe Rosa-e-Silva, Ana Carolina Japur de Sá |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Campos, Jacira Ribeiro Rosa-e-Silva, Julio Cesar Carvalho, Bruno Ramalho Vireque, Alessandra Aparecida Silva-de-Sá, Marcos Felipe Rosa-e-Silva, Ana Carolina Japur de Sá |
dc.subject.por.fl_str_mv |
Ovarian tissue Cryopreservation Tissue damage Ovarian steroidogenesis Tissue culture |
topic |
Ovarian tissue Cryopreservation Tissue damage Ovarian steroidogenesis Tissue culture |
description |
OBJECTIVE: To determine the effect of storage duration on cryopreserved ovarian tissue using fresh and frozenthawed samples. METHODS: Seventeen fertile patients underwent an ovarian biopsy during elective laparoscopic tubal ligation. The tissue sample was divided into three parts: one part was processed fresh (FG), and two were slowly frozen, cryopreserved for 30 (G30) or 180 days (G180), thawed and analyzed. Follicular density, follicular viability, and steroidogenic capacity were assessed. RESULTS: We observed no differences between the groups in follicular density, which was assessed in hematoxylin and eosin-stained tissue sections. A heterogeneous follicular distribution was observed in the parenchyma, with a mean density of 361.3±255.4, 454.9±676.3, and 296.8±269.0 follicles/mm3 for FG, G30 and G180, respectively (p = 0.46). Follicular viability was greater in FG (93.4%) when compared with the cryopreserved tissues (70.8% for G30 (p |
publishDate |
2011 |
dc.date.none.fl_str_mv |
2011-01-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://www.revistas.usp.br/clinics/article/view/19334 10.1590/S1807-59322011001200015 |
url |
https://www.revistas.usp.br/clinics/article/view/19334 |
identifier_str_mv |
10.1590/S1807-59322011001200015 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://www.revistas.usp.br/clinics/article/view/19334/21397 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo |
publisher.none.fl_str_mv |
Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo |
dc.source.none.fl_str_mv |
Clinics; Vol. 66 No. 12 (2011); 2093-2097 Clinics; v. 66 n. 12 (2011); 2093-2097 Clinics; Vol. 66 Núm. 12 (2011); 2093-2097 1980-5322 1807-5932 reponame:Clinics instname:Universidade de São Paulo (USP) instacron:USP |
instname_str |
Universidade de São Paulo (USP) |
instacron_str |
USP |
institution |
USP |
reponame_str |
Clinics |
collection |
Clinics |
repository.name.fl_str_mv |
Clinics - Universidade de São Paulo (USP) |
repository.mail.fl_str_mv |
||clinics@hc.fm.usp.br |
_version_ |
1800222756788240384 |