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Increase in placental apolipoprotein D as an adaptation to human gestational diabetes
The expression of apolipoprotein D (apo D), a lipocalin involved in defense mechanisms against oxidative stress, in placental tissue samples of pregnancies with gestational diabetes mellitus (GDM) was compared to non-diabetic controls. We have investigated the relationship of apo D with 4-HNE, a maj...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Ltd.
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7124627/ https://www.ncbi.nlm.nih.gov/pubmed/19944460 http://dx.doi.org/10.1016/j.placenta.2009.11.002 |
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author | Navarro, A. Alonso, A. Garrido, P. González, C. González del Rey, C. Ordoñez, C. Tolivia, J. |
author_facet | Navarro, A. Alonso, A. Garrido, P. González, C. González del Rey, C. Ordoñez, C. Tolivia, J. |
author_sort | Navarro, A. |
collection | PubMed |
description | The expression of apolipoprotein D (apo D), a lipocalin involved in defense mechanisms against oxidative stress, in placental tissue samples of pregnancies with gestational diabetes mellitus (GDM) was compared to non-diabetic controls. We have investigated the relationship of apo D with 4-HNE, a major propagation product of lipid peroxidation, in stressed tissues. We included 20 pregnant women with GDM and 30 women with normal ongoing pregnancies as the control group. Placentas were collected and frozen for Western blot or included in paraffin for immunohistochemistry. The intensity of immunostaining was higher for apo D and 4-HNE in GDM samples; however, the differences in expression between the groups was more intense for apo D. Positive signals for both antibodies was detected in the villous trophoblast and adventitia tunica around the large blood vessels for all groups. Specific immunostaining for apo D was noted in some mesenchymal and macrophagic-like cells and this signal increased in diabetic placentas. Densitometry analysis of Western blots showed no significant difference for 4-HNE, but was significantly more intense for apo D in diabetic women. The contradictory results for 4-HNE could be due to changes which are too small and are masked in tissue homogenates. The results for apo D showed a strong relationship with GDM in the placenta that may reflect its suggested function in defense mechanisms against oxidative stress. |
format | Online Article Text |
id | pubmed-7124627 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71246272020-04-08 Increase in placental apolipoprotein D as an adaptation to human gestational diabetes Navarro, A. Alonso, A. Garrido, P. González, C. González del Rey, C. Ordoñez, C. Tolivia, J. Placenta Article The expression of apolipoprotein D (apo D), a lipocalin involved in defense mechanisms against oxidative stress, in placental tissue samples of pregnancies with gestational diabetes mellitus (GDM) was compared to non-diabetic controls. We have investigated the relationship of apo D with 4-HNE, a major propagation product of lipid peroxidation, in stressed tissues. We included 20 pregnant women with GDM and 30 women with normal ongoing pregnancies as the control group. Placentas were collected and frozen for Western blot or included in paraffin for immunohistochemistry. The intensity of immunostaining was higher for apo D and 4-HNE in GDM samples; however, the differences in expression between the groups was more intense for apo D. Positive signals for both antibodies was detected in the villous trophoblast and adventitia tunica around the large blood vessels for all groups. Specific immunostaining for apo D was noted in some mesenchymal and macrophagic-like cells and this signal increased in diabetic placentas. Densitometry analysis of Western blots showed no significant difference for 4-HNE, but was significantly more intense for apo D in diabetic women. The contradictory results for 4-HNE could be due to changes which are too small and are masked in tissue homogenates. The results for apo D showed a strong relationship with GDM in the placenta that may reflect its suggested function in defense mechanisms against oxidative stress. Elsevier Ltd. 2010-01 2009-11-26 /pmc/articles/PMC7124627/ /pubmed/19944460 http://dx.doi.org/10.1016/j.placenta.2009.11.002 Text en Copyright © 2009 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Navarro, A. Alonso, A. Garrido, P. González, C. González del Rey, C. Ordoñez, C. Tolivia, J. Increase in placental apolipoprotein D as an adaptation to human gestational diabetes |
title | Increase in placental apolipoprotein D as an adaptation to human gestational diabetes |
title_full | Increase in placental apolipoprotein D as an adaptation to human gestational diabetes |
title_fullStr | Increase in placental apolipoprotein D as an adaptation to human gestational diabetes |
title_full_unstemmed | Increase in placental apolipoprotein D as an adaptation to human gestational diabetes |
title_short | Increase in placental apolipoprotein D as an adaptation to human gestational diabetes |
title_sort | increase in placental apolipoprotein d as an adaptation to human gestational diabetes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7124627/ https://www.ncbi.nlm.nih.gov/pubmed/19944460 http://dx.doi.org/10.1016/j.placenta.2009.11.002 |
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