Cargando…
Nucleated Red Blood Cells as a Marker of Acute and Chronic Fetal Hypoxia in a Rat Model
OBJECTIVE: To examine the relationship between duration of fetal hypoxia, nucleated red blood cell (NRBC) count, and fetal growth. METHODS: Pregnant rats were exposed to a severe hypoxia (9.5%–10% O(2)) for varying time intervals (2, 6, 12, 24, 48, and 120 hours; n=4 for each time interval) immediat...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rambam Health Care Campus
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5415371/ https://www.ncbi.nlm.nih.gov/pubmed/28467759 http://dx.doi.org/10.5041/RMMJ.10302 |
_version_ | 1783233511850770432 |
---|---|
author | Minior, Victoria K. Levine, Brian Ferber, Asaf Guller, Seth Divon, Michael Y. |
author_facet | Minior, Victoria K. Levine, Brian Ferber, Asaf Guller, Seth Divon, Michael Y. |
author_sort | Minior, Victoria K. |
collection | PubMed |
description | OBJECTIVE: To examine the relationship between duration of fetal hypoxia, nucleated red blood cell (NRBC) count, and fetal growth. METHODS: Pregnant rats were exposed to a severe hypoxia (9.5%–10% O(2)) for varying time intervals (2, 6, 12, 24, 48, and 120 hours; n=4 for each time interval) immediately prior to delivery at term. Normoxic controls were exposed to room air (21% O(2)) and matched for all other study variables (n=4 rats for each time interval). Pups were delivered via hysterotomy while maintaining exposure gas concentrations. Blood gas analysis and NRBC counts were performed, and fetal body and liver weights were recorded. Student’s t test and simple regression were used for statistical analysis. RESULTS: As the duration of hypoxia increased, fetal weight, liver weight, blood bicarbonate, and base excess levels decreased significantly; concomitantly, NRBC counts increased. This increase in NRBCs became statistically significant after 24 hours of exposure. After 48 hours of hypoxia there was a 2.5-fold rise in NRBC count, and after 120 hours of hypoxia there was a 4.5-fold rise in NRBC count over control levels. After 12 or more hours of hypoxia, fetal body weights were significantly reduced; 120 hours of hypoxia resulted in a 35% reduction in fetal body weight, a 34% reduction in fetal liver weight, and 356% increase in NRBC count. CONCLUSION: In a pregnant rat model, chronic maternal hypoxia (≥24 hours) results in a significant increase in fetal NRBC counts as well as reduced fetal body weight and organ growth. |
format | Online Article Text |
id | pubmed-5415371 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Rambam Health Care Campus |
record_format | MEDLINE/PubMed |
spelling | pubmed-54153712017-05-10 Nucleated Red Blood Cells as a Marker of Acute and Chronic Fetal Hypoxia in a Rat Model Minior, Victoria K. Levine, Brian Ferber, Asaf Guller, Seth Divon, Michael Y. Rambam Maimonides Med J Special Issue on Gynecology, Fertility, and Obstetrics OBJECTIVE: To examine the relationship between duration of fetal hypoxia, nucleated red blood cell (NRBC) count, and fetal growth. METHODS: Pregnant rats were exposed to a severe hypoxia (9.5%–10% O(2)) for varying time intervals (2, 6, 12, 24, 48, and 120 hours; n=4 for each time interval) immediately prior to delivery at term. Normoxic controls were exposed to room air (21% O(2)) and matched for all other study variables (n=4 rats for each time interval). Pups were delivered via hysterotomy while maintaining exposure gas concentrations. Blood gas analysis and NRBC counts were performed, and fetal body and liver weights were recorded. Student’s t test and simple regression were used for statistical analysis. RESULTS: As the duration of hypoxia increased, fetal weight, liver weight, blood bicarbonate, and base excess levels decreased significantly; concomitantly, NRBC counts increased. This increase in NRBCs became statistically significant after 24 hours of exposure. After 48 hours of hypoxia there was a 2.5-fold rise in NRBC count, and after 120 hours of hypoxia there was a 4.5-fold rise in NRBC count over control levels. After 12 or more hours of hypoxia, fetal body weights were significantly reduced; 120 hours of hypoxia resulted in a 35% reduction in fetal body weight, a 34% reduction in fetal liver weight, and 356% increase in NRBC count. CONCLUSION: In a pregnant rat model, chronic maternal hypoxia (≥24 hours) results in a significant increase in fetal NRBC counts as well as reduced fetal body weight and organ growth. Rambam Health Care Campus 2017-04-28 /pmc/articles/PMC5415371/ /pubmed/28467759 http://dx.doi.org/10.5041/RMMJ.10302 Text en © 2017 Minior et al. This is an open-access article. All its content, except where otherwise noted, is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Special Issue on Gynecology, Fertility, and Obstetrics Minior, Victoria K. Levine, Brian Ferber, Asaf Guller, Seth Divon, Michael Y. Nucleated Red Blood Cells as a Marker of Acute and Chronic Fetal Hypoxia in a Rat Model |
title | Nucleated Red Blood Cells as a Marker of Acute and Chronic Fetal Hypoxia in a Rat Model |
title_full | Nucleated Red Blood Cells as a Marker of Acute and Chronic Fetal Hypoxia in a Rat Model |
title_fullStr | Nucleated Red Blood Cells as a Marker of Acute and Chronic Fetal Hypoxia in a Rat Model |
title_full_unstemmed | Nucleated Red Blood Cells as a Marker of Acute and Chronic Fetal Hypoxia in a Rat Model |
title_short | Nucleated Red Blood Cells as a Marker of Acute and Chronic Fetal Hypoxia in a Rat Model |
title_sort | nucleated red blood cells as a marker of acute and chronic fetal hypoxia in a rat model |
topic | Special Issue on Gynecology, Fertility, and Obstetrics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5415371/ https://www.ncbi.nlm.nih.gov/pubmed/28467759 http://dx.doi.org/10.5041/RMMJ.10302 |
work_keys_str_mv | AT miniorvictoriak nucleatedredbloodcellsasamarkerofacuteandchronicfetalhypoxiainaratmodel AT levinebrian nucleatedredbloodcellsasamarkerofacuteandchronicfetalhypoxiainaratmodel AT ferberasaf nucleatedredbloodcellsasamarkerofacuteandchronicfetalhypoxiainaratmodel AT gullerseth nucleatedredbloodcellsasamarkerofacuteandchronicfetalhypoxiainaratmodel AT divonmichaely nucleatedredbloodcellsasamarkerofacuteandchronicfetalhypoxiainaratmodel |