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Sleep restriction during pregnancy and its effects on blood pressure and renal function among female offspring

The influence of sleep restriction (SR) during pregnancy on blood pressure and renal function among female adult offspring was investigated. Pregnant Wistar rats were distributed into control and SR groups. The SR was performed between the 14th and 20th days of pregnancy (multiple platforms method f...

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Autores principales: Argeri, Rogério, Nishi, Erika E., Volpini, Rildo A., Palma, Beatriz D., Tufik, Sergio, Gomes, Guiomar N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5002907/
https://www.ncbi.nlm.nih.gov/pubmed/27796270
http://dx.doi.org/10.14814/phy2.12888
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author Argeri, Rogério
Nishi, Erika E.
Volpini, Rildo A.
Palma, Beatriz D.
Tufik, Sergio
Gomes, Guiomar N.
author_facet Argeri, Rogério
Nishi, Erika E.
Volpini, Rildo A.
Palma, Beatriz D.
Tufik, Sergio
Gomes, Guiomar N.
author_sort Argeri, Rogério
collection PubMed
description The influence of sleep restriction (SR) during pregnancy on blood pressure and renal function among female adult offspring was investigated. Pregnant Wistar rats were distributed into control and SR groups. The SR was performed between the 14th and 20th days of pregnancy (multiple platforms method for 20 h/day). At 2 months of age, half of the offspring from both groups were subjected to an ovariectomy (ovx), and the other half underwent sham surgery. The groups were as follows: control sham (C(sham)), control ovx (C(ovx)), SR sham (SR (sham)), and SR ovx (SR (ovx)). Renal function markers and systolic blood pressure (BPi, indirect method) were evaluated at 4, 6, and 8 months. Subsequently, the rats were euthanized, kidneys were removed, and processed for morphological analyses of glomerular area (GA), number of glomeruli per mm(3) (NG), and kidney mass (KM). Increased BPi was observed in the C(ovx), SR (sham), and SR (ovx) groups compared to C(sham) at all ages. Increased plasma creatinine concentration and decreased creatinine clearance were observed in the SR (sham) and SR (ovx) groups compared to the C(sham) and C(ovx) groups. The SR (ovx) group showed higher BPi and reduced creatinine clearance compared to all other groups. The SR (ovx) group showed reduced values of GA and KM, as well as increased NG, macrophage infiltration, collagen deposit, and ACE1 expression at the renal cortex. Therefore, SR during pregnancy might be an additional risk factor for developing renal dysfunction and increasing BP in female adult offspring. The absence of female hormones exacerbates the changes caused by SR.
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spelling pubmed-50029072016-09-07 Sleep restriction during pregnancy and its effects on blood pressure and renal function among female offspring Argeri, Rogério Nishi, Erika E. Volpini, Rildo A. Palma, Beatriz D. Tufik, Sergio Gomes, Guiomar N. Physiol Rep Original Research The influence of sleep restriction (SR) during pregnancy on blood pressure and renal function among female adult offspring was investigated. Pregnant Wistar rats were distributed into control and SR groups. The SR was performed between the 14th and 20th days of pregnancy (multiple platforms method for 20 h/day). At 2 months of age, half of the offspring from both groups were subjected to an ovariectomy (ovx), and the other half underwent sham surgery. The groups were as follows: control sham (C(sham)), control ovx (C(ovx)), SR sham (SR (sham)), and SR ovx (SR (ovx)). Renal function markers and systolic blood pressure (BPi, indirect method) were evaluated at 4, 6, and 8 months. Subsequently, the rats were euthanized, kidneys were removed, and processed for morphological analyses of glomerular area (GA), number of glomeruli per mm(3) (NG), and kidney mass (KM). Increased BPi was observed in the C(ovx), SR (sham), and SR (ovx) groups compared to C(sham) at all ages. Increased plasma creatinine concentration and decreased creatinine clearance were observed in the SR (sham) and SR (ovx) groups compared to the C(sham) and C(ovx) groups. The SR (ovx) group showed higher BPi and reduced creatinine clearance compared to all other groups. The SR (ovx) group showed reduced values of GA and KM, as well as increased NG, macrophage infiltration, collagen deposit, and ACE1 expression at the renal cortex. Therefore, SR during pregnancy might be an additional risk factor for developing renal dysfunction and increasing BP in female adult offspring. The absence of female hormones exacerbates the changes caused by SR. John Wiley and Sons Inc. 2016-08-22 /pmc/articles/PMC5002907/ /pubmed/27796270 http://dx.doi.org/10.14814/phy2.12888 Text en © 2016 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of the American Physiological Society and The 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
Argeri, Rogério
Nishi, Erika E.
Volpini, Rildo A.
Palma, Beatriz D.
Tufik, Sergio
Gomes, Guiomar N.
Sleep restriction during pregnancy and its effects on blood pressure and renal function among female offspring
title Sleep restriction during pregnancy and its effects on blood pressure and renal function among female offspring
title_full Sleep restriction during pregnancy and its effects on blood pressure and renal function among female offspring
title_fullStr Sleep restriction during pregnancy and its effects on blood pressure and renal function among female offspring
title_full_unstemmed Sleep restriction during pregnancy and its effects on blood pressure and renal function among female offspring
title_short Sleep restriction during pregnancy and its effects on blood pressure and renal function among female offspring
title_sort sleep restriction during pregnancy and its effects on blood pressure and renal function among female offspring
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5002907/
https://www.ncbi.nlm.nih.gov/pubmed/27796270
http://dx.doi.org/10.14814/phy2.12888
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