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In vivo arginine production and nitric oxide synthesis in pregnant Indian women with normal and low body mass indices

BACKGROUND/OBJECTIVES: Nitric oxide (NO) has been proposed as a mediator of vascular expansion during pregnancy. Inability to increase NO synthesis and/or production of its precursor, arginine, may be a contributor to pregnancy-induced hypertension or preeclampsia. Because maternal weight is associa...

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Autores principales: Kurpad, A V, Kao, C, Dwarkanath, P, Muthayya, S, Mhaskar, A, Thomas, A, Vaz, M, Jahoor, F
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2834371/
https://www.ncbi.nlm.nih.gov/pubmed/19436322
http://dx.doi.org/10.1038/ejcn.2009.24
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author Kurpad, A V
Kao, C
Dwarkanath, P
Muthayya, S
Mhaskar, A
Thomas, A
Vaz, M
Jahoor, F
author_facet Kurpad, A V
Kao, C
Dwarkanath, P
Muthayya, S
Mhaskar, A
Thomas, A
Vaz, M
Jahoor, F
author_sort Kurpad, A V
collection PubMed
description BACKGROUND/OBJECTIVES: Nitric oxide (NO) has been proposed as a mediator of vascular expansion during pregnancy. Inability to increase NO synthesis and/or production of its precursor, arginine, may be a contributor to pregnancy-induced hypertension or preeclampsia. Because maternal weight is associated with blood pressure and risk of preeclampsia during pregnancy, it may also influence arginine and/or NO production. The purpose of this study was to determine the in vivo arginine production and NO synthesis rate in pregnant women with normal (n=10) and low (n=10) body mass indices (BMIs). SUBJECTS/METHODS: Arginine flux and NO synthesis rate were measured in the postabsorptive state with constant infusions of (15)N(2)-arginine and (13)C,(2)H(4)-citrulline. Plasma concentrations of arginine and NO metabolites were also measured. Kinetic parameters were correlated to maternal variables, gestational age, birth weight and blood pressure. RESULTS: Endogenous arginine flux was significantly faster in the low-BMI compared with normal-BMI women in the first trimester (63.1±3.4 vs 50.2±2.0 μmol/kg per h, P<0.01), but not in the second. Plasma NO concentration was higher (44.7±5.3 vs 30.4±1.9 μmol/l, P=0.03) and its rate of synthesis trended faster in the low-BMI compared with normal-BMI group in the second trimester. Maternal weight and BMI were negatively correlated with arginine flux in both trimesters and NO synthesis in the second trimester. CONCLUSIONS: These findings suggest, but do not prove, that maternal BMI may be a factor in the ability to produce NO during pregnancy and may be one way by which BMI influences blood pressure during pregnancy.
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spelling pubmed-28343712010-03-29 In vivo arginine production and nitric oxide synthesis in pregnant Indian women with normal and low body mass indices Kurpad, A V Kao, C Dwarkanath, P Muthayya, S Mhaskar, A Thomas, A Vaz, M Jahoor, F Eur J Clin Nutr Original Articles BACKGROUND/OBJECTIVES: Nitric oxide (NO) has been proposed as a mediator of vascular expansion during pregnancy. Inability to increase NO synthesis and/or production of its precursor, arginine, may be a contributor to pregnancy-induced hypertension or preeclampsia. Because maternal weight is associated with blood pressure and risk of preeclampsia during pregnancy, it may also influence arginine and/or NO production. The purpose of this study was to determine the in vivo arginine production and NO synthesis rate in pregnant women with normal (n=10) and low (n=10) body mass indices (BMIs). SUBJECTS/METHODS: Arginine flux and NO synthesis rate were measured in the postabsorptive state with constant infusions of (15)N(2)-arginine and (13)C,(2)H(4)-citrulline. Plasma concentrations of arginine and NO metabolites were also measured. Kinetic parameters were correlated to maternal variables, gestational age, birth weight and blood pressure. RESULTS: Endogenous arginine flux was significantly faster in the low-BMI compared with normal-BMI women in the first trimester (63.1±3.4 vs 50.2±2.0 μmol/kg per h, P<0.01), but not in the second. Plasma NO concentration was higher (44.7±5.3 vs 30.4±1.9 μmol/l, P=0.03) and its rate of synthesis trended faster in the low-BMI compared with normal-BMI group in the second trimester. Maternal weight and BMI were negatively correlated with arginine flux in both trimesters and NO synthesis in the second trimester. CONCLUSIONS: These findings suggest, but do not prove, that maternal BMI may be a factor in the ability to produce NO during pregnancy and may be one way by which BMI influences blood pressure during pregnancy. Nature Publishing Group 2009-05-13 2009-09 /pmc/articles/PMC2834371/ /pubmed/19436322 http://dx.doi.org/10.1038/ejcn.2009.24 Text en Copyright 2009, Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-No Derivative Works 3.0 Licence. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Original Articles
Kurpad, A V
Kao, C
Dwarkanath, P
Muthayya, S
Mhaskar, A
Thomas, A
Vaz, M
Jahoor, F
In vivo arginine production and nitric oxide synthesis in pregnant Indian women with normal and low body mass indices
title In vivo arginine production and nitric oxide synthesis in pregnant Indian women with normal and low body mass indices
title_full In vivo arginine production and nitric oxide synthesis in pregnant Indian women with normal and low body mass indices
title_fullStr In vivo arginine production and nitric oxide synthesis in pregnant Indian women with normal and low body mass indices
title_full_unstemmed In vivo arginine production and nitric oxide synthesis in pregnant Indian women with normal and low body mass indices
title_short In vivo arginine production and nitric oxide synthesis in pregnant Indian women with normal and low body mass indices
title_sort in vivo arginine production and nitric oxide synthesis in pregnant indian women with normal and low body mass indices
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2834371/
https://www.ncbi.nlm.nih.gov/pubmed/19436322
http://dx.doi.org/10.1038/ejcn.2009.24
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