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Transient enalapril attenuates the reduction in glomerular filtration rate in prenatally programmed rats
A maternal low‐protein diet has been shown to program hypertension and a reduction in glomerular filtration rate in adult offspring. This study examined the effect of continuous administration of enalapril in the drinking water and transient administration of enalapril administered from 21 to 42 day...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5408291/ https://www.ncbi.nlm.nih.gov/pubmed/28438986 http://dx.doi.org/10.14814/phy2.13266 |
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author | Mansuri, Asifhusen Elmaghrabi, Ayah Alhamoud, Issa Legan, Susan K. Gattineni, Jyothsna Baum, Michel |
author_facet | Mansuri, Asifhusen Elmaghrabi, Ayah Alhamoud, Issa Legan, Susan K. Gattineni, Jyothsna Baum, Michel |
author_sort | Mansuri, Asifhusen |
collection | PubMed |
description | A maternal low‐protein diet has been shown to program hypertension and a reduction in glomerular filtration rate in adult offspring. This study examined the effect of continuous administration of enalapril in the drinking water and transient administration of enalapril administered from 21 to 42 days of age on blood pressure and glomerular filtration rate (GFR) in male rats whose mothers were fed a 20% protein diet (control) or a 6% protein diet (programmed) during the last half of pregnancy. After birth all rats were fed a 20% protein diet. Programmed rats (maternal 6% protein diet) were hypertensive at 15 months of age compared to control rats and both continuous and transient administration of enalapril had no effect on blood pressure on control offspring, but normalized the blood pressure of programmed offspring. GFR was 3.2 ± 0.1 mL/min in the control group and 1.7 ± 0.1 mL/min in the programmed rats at 17 months of age (P < 0.001). The GFR was 3.0 ± 0.1 mL/min in the control and 2.7 ± 0.1 mL/min in the programmed group that received continuous enalapril in their drinking water showing that enalapril can prevent the decrease in GFR in programmed rats. Transient administration of enalapril had no effect on GFR in the control group (3.2 ± 0.1 mL/min) and prevented the decrease in GFR in the programmed group (2.9 ± 0.1 mL/min). In conclusion, transient exposure to enalapril for 3 weeks after weaning can prevent the hypertension and decrease in GFR in prenatal programmed rats. |
format | Online Article Text |
id | pubmed-5408291 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-54082912017-05-02 Transient enalapril attenuates the reduction in glomerular filtration rate in prenatally programmed rats Mansuri, Asifhusen Elmaghrabi, Ayah Alhamoud, Issa Legan, Susan K. Gattineni, Jyothsna Baum, Michel Physiol Rep Original Research A maternal low‐protein diet has been shown to program hypertension and a reduction in glomerular filtration rate in adult offspring. This study examined the effect of continuous administration of enalapril in the drinking water and transient administration of enalapril administered from 21 to 42 days of age on blood pressure and glomerular filtration rate (GFR) in male rats whose mothers were fed a 20% protein diet (control) or a 6% protein diet (programmed) during the last half of pregnancy. After birth all rats were fed a 20% protein diet. Programmed rats (maternal 6% protein diet) were hypertensive at 15 months of age compared to control rats and both continuous and transient administration of enalapril had no effect on blood pressure on control offspring, but normalized the blood pressure of programmed offspring. GFR was 3.2 ± 0.1 mL/min in the control group and 1.7 ± 0.1 mL/min in the programmed rats at 17 months of age (P < 0.001). The GFR was 3.0 ± 0.1 mL/min in the control and 2.7 ± 0.1 mL/min in the programmed group that received continuous enalapril in their drinking water showing that enalapril can prevent the decrease in GFR in programmed rats. Transient administration of enalapril had no effect on GFR in the control group (3.2 ± 0.1 mL/min) and prevented the decrease in GFR in the programmed group (2.9 ± 0.1 mL/min). In conclusion, transient exposure to enalapril for 3 weeks after weaning can prevent the hypertension and decrease in GFR in prenatal programmed rats. John Wiley and Sons Inc. 2017-04-24 /pmc/articles/PMC5408291/ /pubmed/28438986 http://dx.doi.org/10.14814/phy2.13266 Text en © 2017 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Mansuri, Asifhusen Elmaghrabi, Ayah Alhamoud, Issa Legan, Susan K. Gattineni, Jyothsna Baum, Michel Transient enalapril attenuates the reduction in glomerular filtration rate in prenatally programmed rats |
title | Transient enalapril attenuates the reduction in glomerular filtration rate in prenatally programmed rats |
title_full | Transient enalapril attenuates the reduction in glomerular filtration rate in prenatally programmed rats |
title_fullStr | Transient enalapril attenuates the reduction in glomerular filtration rate in prenatally programmed rats |
title_full_unstemmed | Transient enalapril attenuates the reduction in glomerular filtration rate in prenatally programmed rats |
title_short | Transient enalapril attenuates the reduction in glomerular filtration rate in prenatally programmed rats |
title_sort | transient enalapril attenuates the reduction in glomerular filtration rate in prenatally programmed rats |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5408291/ https://www.ncbi.nlm.nih.gov/pubmed/28438986 http://dx.doi.org/10.14814/phy2.13266 |
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