The University of Southampton
University of Southampton Institutional Repository

Vascular, renal and placental effects on pregnant offspring of protein-restricted rat dams

Vascular, renal and placental effects on pregnant offspring of protein-restricted rat dams
Vascular, renal and placental effects on pregnant offspring of protein-restricted rat dams
Aim: Our previous study showed that a maternal low-protein diet induced hypertension and vascular dysfunction in rat offspring after day 175. In the present study, we hypothesized that these female offspring would develop hypertension in their own pregnancies even at ages less than 175 days because potential vascular dysfunction is exacerbated by the circulatory demands of pregnancy.

Material and Methods: Wistar rats were fed an isocaloric diet containing either 18% (control group) or 9% (low-protein group) casein throughout pregnancy. The female offspring were fed standard chow and mated between days 70 and 125. At the end of pregnancy, blood pressure was measured, and the uterine arteries were dissected and investigated with a wire myograph.

Results: Placental weights were significantly lower in offspring of the low-protein group versus control. There
were no significant differences in blood pressure. Renal expression of AT1 receptor mRNA was greater, and of AT2 receptor was less, in the low-protein group versus control. Vasoconstriction of uterine arteries to phenylephrine and U46619 was increased in the low-protein group, and vasodilatation to sodium nitroprusside was also increased.

Conclusion: Low-protein diet induces vascular effects on female offspring in their pregnancy, in terms of increased uterine artery vasoconstriction. This may be compensated for by increased sensitivity to nitric oxide (NO), maintaining blood pressure normal in the face of the demands of pregnancy. Such renal and vascular effects, combined with placental size, may transmit risk of vascular dysfunction to subsequent generations.
hypertension, preeclampsia, pregnancy, protein restriction, vascular dysfunction
1341-8076
343-351
Musha, Yuka
9fb27b38-85d2-4834-a16a-5fb8b134d876
Itoh, Shigeru
ee32ea77-f41b-486b-a687-dae80f4a244e
Miyakawa, Miho
d828f1c3-5406-4849-9e4d-eb22caaa4717
Ohtsuji, Mareki
b06e17ac-0619-48f6-8c96-e921deebf627
Hanson, Mark A.
1952fad1-abc7-4284-a0bc-a7eb31f70a3f
Kinoshita, Katsuyuki
f74b7f1a-d661-4ecc-8287-da17fc0b124b
Takeda, Satoru
b79f53fe-025e-4076-ab0f-18a748505cbd
Musha, Yuka
9fb27b38-85d2-4834-a16a-5fb8b134d876
Itoh, Shigeru
ee32ea77-f41b-486b-a687-dae80f4a244e
Miyakawa, Miho
d828f1c3-5406-4849-9e4d-eb22caaa4717
Ohtsuji, Mareki
b06e17ac-0619-48f6-8c96-e921deebf627
Hanson, Mark A.
1952fad1-abc7-4284-a0bc-a7eb31f70a3f
Kinoshita, Katsuyuki
f74b7f1a-d661-4ecc-8287-da17fc0b124b
Takeda, Satoru
b79f53fe-025e-4076-ab0f-18a748505cbd

Musha, Yuka, Itoh, Shigeru, Miyakawa, Miho, Ohtsuji, Mareki, Hanson, Mark A., Kinoshita, Katsuyuki and Takeda, Satoru (2011) Vascular, renal and placental effects on pregnant offspring of protein-restricted rat dams. Journal of Obstetrics and Gynaecology Research, 37 (4), 343-351. (doi:10.1111/j.1447-0756.2010.01351.x). (PMID:21272146)

Record type: Article

Abstract

Aim: Our previous study showed that a maternal low-protein diet induced hypertension and vascular dysfunction in rat offspring after day 175. In the present study, we hypothesized that these female offspring would develop hypertension in their own pregnancies even at ages less than 175 days because potential vascular dysfunction is exacerbated by the circulatory demands of pregnancy.

Material and Methods: Wistar rats were fed an isocaloric diet containing either 18% (control group) or 9% (low-protein group) casein throughout pregnancy. The female offspring were fed standard chow and mated between days 70 and 125. At the end of pregnancy, blood pressure was measured, and the uterine arteries were dissected and investigated with a wire myograph.

Results: Placental weights were significantly lower in offspring of the low-protein group versus control. There
were no significant differences in blood pressure. Renal expression of AT1 receptor mRNA was greater, and of AT2 receptor was less, in the low-protein group versus control. Vasoconstriction of uterine arteries to phenylephrine and U46619 was increased in the low-protein group, and vasodilatation to sodium nitroprusside was also increased.

Conclusion: Low-protein diet induces vascular effects on female offspring in their pregnancy, in terms of increased uterine artery vasoconstriction. This may be compensated for by increased sensitivity to nitric oxide (NO), maintaining blood pressure normal in the face of the demands of pregnancy. Such renal and vascular effects, combined with placental size, may transmit risk of vascular dysfunction to subsequent generations.

This record has no associated files available for download.

More information

Published date: April 2011
Keywords: hypertension, preeclampsia, pregnancy, protein restriction, vascular dysfunction
Organisations: Human Development & Health

Identifiers

Local EPrints ID: 337116
URI: http://eprints.soton.ac.uk/id/eprint/337116
ISSN: 1341-8076
PURE UUID: 62c628f7-6cf4-4f6b-af42-00b1fa7d3861
ORCID for Mark A. Hanson: ORCID iD orcid.org/0000-0002-6907-613X

Catalogue record

Date deposited: 18 Apr 2012 13:01
Last modified: 15 Mar 2024 03:07

Export record

Altmetrics

Contributors

Author: Yuka Musha
Author: Shigeru Itoh
Author: Miho Miyakawa
Author: Mareki Ohtsuji
Author: Mark A. Hanson ORCID iD
Author: Katsuyuki Kinoshita
Author: Satoru Takeda

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×