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Endothelial dysfunction and reduced antioxidant protection in an animal model of the developmental origins of cardiovascular disease

Endothelial dysfunction and reduced antioxidant protection in an animal model of the developmental origins of cardiovascular disease
Endothelial dysfunction and reduced antioxidant protection in an animal model of the developmental origins of cardiovascular disease
Endothelial dysfunction underlies cardiovascular disease (CVD) in humans and is reported in animal models of developmental origins of such disease. We have investigated whether impaired antioxidant defences and NO generation underlie the genesis of endothelial dysfunction and operate as part of the normal processes of developmental plasticity regulating the induction of phenotype in the offspring. Female Wistar rats were fed either a control (C, 18% protein) or protein-restricted (PR, 9% protein) diet throughout pregnancy. Dams and pups were returned to standard laboratory chow post partum. In male offspring, PR resulted in a reduced endothelial responsiveness to acetylcholine (P < 0.05) in resistance arteries, with vascular remodelling evident from a reduction in smooth muscle content. mRNA expression of endothelial NO synthase (eNOS) was increased (P < 0.05) but there was no change in mRNA levels of manganese superoxide dismutase (MnSOD) or glutamate cysteine ligase (GCL) expression. Interestingly, expression of the antioxidant enzyme haem oxygenase-1 (HO-1) was reduced in the liver (P < 0.05). Female PR offspring also showed a reduced endothelial responsiveness but exhibited no changes in expression of eNOS, iNOS, soluble guanylate cyclase (sGC) or antioxidant genes. Thus, in this model of the developmental origins of CVD, the structure and function of resistance arteries in offspring is altered in complex ways which cannot simply be explained by attenuation in vascular eNOS or in antioxidant protection afforded by GCL or MnSOD. The dysfunction in male offspring may partially be counteracted by an up-regulation of eNOS expression; however, PR does lead to reduced HO-1 expression in these offspring, which may affect both their growth and vascular function. Our findings have established that PR induces significant phenotypic changes in male offspring that may be indicative of an adaptive response during development
growth, diet, physiopathology, vascular, animals, protein carbonylation, nitric oxide synthase, nitric oxide synthase type ii, cardiovascular-disease, nitric oxide, metabolism, guanylate cyclase, rna, mesenteric arteries, hemodynamics, male, blood, disease, wistar, female, rats, pathology, expression, human, etiology, humans, muscle, organ size, acetylcholine, gene, weight gain, protein-restricted, homocysteine, antioxidants, research, cardiovascular diseases, developmental origins, messenger, developmental plasticity, gene expression regulation, phenotype, protein, developmental, up-regulation, nitric oxide synthase type iii, development, reduction, blood pressure, endothelium, liver, pregnancy, cardiovascular disease, sex characteristics, adverse effects
0022-3751
4709-4720
Rodford, Joanne L.
27b067f0-55e6-4f1b-807b-f9ca5a06bf78
Torrens, Christopher
15a35713-0651-4249-8227-5901e2cfcd22
Siow, Richard C.M.
883c03d4-9554-4df4-a662-56046181047a
Mann, Giovanni E.
fff59a0d-4539-45c4-9a77-65dea88ccb9d
Hanson, Mark A.
1952fad1-abc7-4284-a0bc-a7eb31f70a3f
Clough, Geraldine F.
9f19639e-a929-4976-ac35-259f9011c494
Rodford, Joanne L.
27b067f0-55e6-4f1b-807b-f9ca5a06bf78
Torrens, Christopher
15a35713-0651-4249-8227-5901e2cfcd22
Siow, Richard C.M.
883c03d4-9554-4df4-a662-56046181047a
Mann, Giovanni E.
fff59a0d-4539-45c4-9a77-65dea88ccb9d
Hanson, Mark A.
1952fad1-abc7-4284-a0bc-a7eb31f70a3f
Clough, Geraldine F.
9f19639e-a929-4976-ac35-259f9011c494

Rodford, Joanne L., Torrens, Christopher, Siow, Richard C.M., Mann, Giovanni E., Hanson, Mark A. and Clough, Geraldine F. (2008) Endothelial dysfunction and reduced antioxidant protection in an animal model of the developmental origins of cardiovascular disease. Journal of Physiology, 586 (19), 4709-4720. (doi:10.1113/jphysiol.2008.156976).

Record type: Article

Abstract

Endothelial dysfunction underlies cardiovascular disease (CVD) in humans and is reported in animal models of developmental origins of such disease. We have investigated whether impaired antioxidant defences and NO generation underlie the genesis of endothelial dysfunction and operate as part of the normal processes of developmental plasticity regulating the induction of phenotype in the offspring. Female Wistar rats were fed either a control (C, 18% protein) or protein-restricted (PR, 9% protein) diet throughout pregnancy. Dams and pups were returned to standard laboratory chow post partum. In male offspring, PR resulted in a reduced endothelial responsiveness to acetylcholine (P < 0.05) in resistance arteries, with vascular remodelling evident from a reduction in smooth muscle content. mRNA expression of endothelial NO synthase (eNOS) was increased (P < 0.05) but there was no change in mRNA levels of manganese superoxide dismutase (MnSOD) or glutamate cysteine ligase (GCL) expression. Interestingly, expression of the antioxidant enzyme haem oxygenase-1 (HO-1) was reduced in the liver (P < 0.05). Female PR offspring also showed a reduced endothelial responsiveness but exhibited no changes in expression of eNOS, iNOS, soluble guanylate cyclase (sGC) or antioxidant genes. Thus, in this model of the developmental origins of CVD, the structure and function of resistance arteries in offspring is altered in complex ways which cannot simply be explained by attenuation in vascular eNOS or in antioxidant protection afforded by GCL or MnSOD. The dysfunction in male offspring may partially be counteracted by an up-regulation of eNOS expression; however, PR does lead to reduced HO-1 expression in these offspring, which may affect both their growth and vascular function. Our findings have established that PR induces significant phenotypic changes in male offspring that may be indicative of an adaptive response during development

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e-pub ahead of print date: 31 July 2008
Published date: 2008
Keywords: growth, diet, physiopathology, vascular, animals, protein carbonylation, nitric oxide synthase, nitric oxide synthase type ii, cardiovascular-disease, nitric oxide, metabolism, guanylate cyclase, rna, mesenteric arteries, hemodynamics, male, blood, disease, wistar, female, rats, pathology, expression, human, etiology, humans, muscle, organ size, acetylcholine, gene, weight gain, protein-restricted, homocysteine, antioxidants, research, cardiovascular diseases, developmental origins, messenger, developmental plasticity, gene expression regulation, phenotype, protein, developmental, up-regulation, nitric oxide synthase type iii, development, reduction, blood pressure, endothelium, liver, pregnancy, cardiovascular disease, sex characteristics, adverse effects
Organisations: Dev Origins of Health & Disease

Identifiers

Local EPrints ID: 70522
URI: http://eprints.soton.ac.uk/id/eprint/70522
ISSN: 0022-3751
PURE UUID: 25fb6109-9ba7-4cad-979d-fccad94a7910
ORCID for Mark A. Hanson: ORCID iD orcid.org/0000-0002-6907-613X
ORCID for Geraldine F. Clough: ORCID iD orcid.org/0000-0002-6226-8964

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Date deposited: 03 Feb 2010
Last modified: 14 Mar 2024 02:44

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Contributors

Author: Joanne L. Rodford
Author: Christopher Torrens
Author: Richard C.M. Siow
Author: Giovanni E. Mann
Author: Mark A. Hanson ORCID iD

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