Cargando…

Divergence of mechanistic pathways mediating cardiovascular aging and developmental programming of cardiovascular disease

Aging and developmental programming are both associated with oxidative stress and endothelial dysfunction, suggesting common mechanistic origins. However, their interrelationship has been little explored. In a rodent model of programmed cardiovascular dysfunction we determined endothelial function a...

Descripción completa

Detalles Bibliográficos
Autores principales: Allison, Beth J., Kaandorp, Joepe J., Kane, Andrew D., Camm, Emily J., Lusby, Ciara, Cross, Christine M., Nevin-Dolan, Rhianon, Thakor, Avnesh S., Derks, Jan B., Tarry-Adkins, Jane L., Ozanne, Susan E., Giussani, Dino A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Federation of American Societies for Experimental Biology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5036970/
https://www.ncbi.nlm.nih.gov/pubmed/26932929
http://dx.doi.org/10.1096/fj.201500057
_version_ 1782455654709985280
author Allison, Beth J.
Kaandorp, Joepe J.
Kane, Andrew D.
Camm, Emily J.
Lusby, Ciara
Cross, Christine M.
Nevin-Dolan, Rhianon
Thakor, Avnesh S.
Derks, Jan B.
Tarry-Adkins, Jane L.
Ozanne, Susan E.
Giussani, Dino A.
author_facet Allison, Beth J.
Kaandorp, Joepe J.
Kane, Andrew D.
Camm, Emily J.
Lusby, Ciara
Cross, Christine M.
Nevin-Dolan, Rhianon
Thakor, Avnesh S.
Derks, Jan B.
Tarry-Adkins, Jane L.
Ozanne, Susan E.
Giussani, Dino A.
author_sort Allison, Beth J.
collection PubMed
description Aging and developmental programming are both associated with oxidative stress and endothelial dysfunction, suggesting common mechanistic origins. However, their interrelationship has been little explored. In a rodent model of programmed cardiovascular dysfunction we determined endothelial function and vascular telomere length in young (4 mo) and aged (15 mo) adult offspring of normoxic or hypoxic pregnancy with or without maternal antioxidant treatment. We show loss of endothelial function [maximal arterial relaxation to acetylcholine (71 ± 3 vs. 55 ± 3%) and increased vascular short telomere abundance (4.2–1.3 kb) 43.0 ± 1.5 vs. 55.1 ± 3.8%) in aged vs. young offspring of normoxic pregnancy (P < 0.05). Hypoxic pregnancy in young offspring accelerated endothelial dysfunction (maximal arterial relaxation to acetylcholine: 42 ± 1%, P < 0.05) but this was dissociated from increased vascular short telomere length abundance. Maternal allopurinol rescued maximal arterial relaxation to acetylcholine in aged offspring of normoxic or hypoxic pregnancy but not in young offspring of hypoxic pregnancy. Aged offspring of hypoxic allopurinol pregnancy compared with aged offspring of untreated hypoxic pregnancy had lower levels of short telomeres (vascular short telomere length abundance 35.1 ± 2.5 vs. 48.2 ± 2.6%) and of plasma proinflammatory chemokine (24.6 ± 2.8 vs. 36.8 ± 5.5 pg/ml, P < 0.05). These data provide evidence for divergence of mechanistic pathways mediating cardiovascular aging and developmental programming of cardiovascular disease, and aging being decelerated by antioxidants even prior to birth.—Allison, B. J., Kaandorp, J. J., Kane, A. D., Camm, E. J., Lusby, C., Cross, C. M., Nevin-Dolan, R., Thakor, A. S., Derks, J. B., Tarry-Adkins, J. L., Ozanne, S. E., Giussani, D. A. Divergence of mechanistic pathways mediating cardiovascular aging and developmental programming of cardiovascular disease.
format Online
Article
Text
id pubmed-5036970
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Federation of American Societies for Experimental Biology
record_format MEDLINE/PubMed
spelling pubmed-50369702016-09-29 Divergence of mechanistic pathways mediating cardiovascular aging and developmental programming of cardiovascular disease Allison, Beth J. Kaandorp, Joepe J. Kane, Andrew D. Camm, Emily J. Lusby, Ciara Cross, Christine M. Nevin-Dolan, Rhianon Thakor, Avnesh S. Derks, Jan B. Tarry-Adkins, Jane L. Ozanne, Susan E. Giussani, Dino A. FASEB J Research Communication Aging and developmental programming are both associated with oxidative stress and endothelial dysfunction, suggesting common mechanistic origins. However, their interrelationship has been little explored. In a rodent model of programmed cardiovascular dysfunction we determined endothelial function and vascular telomere length in young (4 mo) and aged (15 mo) adult offspring of normoxic or hypoxic pregnancy with or without maternal antioxidant treatment. We show loss of endothelial function [maximal arterial relaxation to acetylcholine (71 ± 3 vs. 55 ± 3%) and increased vascular short telomere abundance (4.2–1.3 kb) 43.0 ± 1.5 vs. 55.1 ± 3.8%) in aged vs. young offspring of normoxic pregnancy (P < 0.05). Hypoxic pregnancy in young offspring accelerated endothelial dysfunction (maximal arterial relaxation to acetylcholine: 42 ± 1%, P < 0.05) but this was dissociated from increased vascular short telomere length abundance. Maternal allopurinol rescued maximal arterial relaxation to acetylcholine in aged offspring of normoxic or hypoxic pregnancy but not in young offspring of hypoxic pregnancy. Aged offspring of hypoxic allopurinol pregnancy compared with aged offspring of untreated hypoxic pregnancy had lower levels of short telomeres (vascular short telomere length abundance 35.1 ± 2.5 vs. 48.2 ± 2.6%) and of plasma proinflammatory chemokine (24.6 ± 2.8 vs. 36.8 ± 5.5 pg/ml, P < 0.05). These data provide evidence for divergence of mechanistic pathways mediating cardiovascular aging and developmental programming of cardiovascular disease, and aging being decelerated by antioxidants even prior to birth.—Allison, B. J., Kaandorp, J. J., Kane, A. D., Camm, E. J., Lusby, C., Cross, C. M., Nevin-Dolan, R., Thakor, A. S., Derks, J. B., Tarry-Adkins, J. L., Ozanne, S. E., Giussani, D. A. Divergence of mechanistic pathways mediating cardiovascular aging and developmental programming of cardiovascular disease. Federation of American Societies for Experimental Biology 2016-03-01 2016-05 /pmc/articles/PMC5036970/ /pubmed/26932929 http://dx.doi.org/10.1096/fj.201500057 Text en © The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 International (CC BY 4.0) (http://creativecommons.org/licenses/by/4.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Communication
Allison, Beth J.
Kaandorp, Joepe J.
Kane, Andrew D.
Camm, Emily J.
Lusby, Ciara
Cross, Christine M.
Nevin-Dolan, Rhianon
Thakor, Avnesh S.
Derks, Jan B.
Tarry-Adkins, Jane L.
Ozanne, Susan E.
Giussani, Dino A.
Divergence of mechanistic pathways mediating cardiovascular aging and developmental programming of cardiovascular disease
title Divergence of mechanistic pathways mediating cardiovascular aging and developmental programming of cardiovascular disease
title_full Divergence of mechanistic pathways mediating cardiovascular aging and developmental programming of cardiovascular disease
title_fullStr Divergence of mechanistic pathways mediating cardiovascular aging and developmental programming of cardiovascular disease
title_full_unstemmed Divergence of mechanistic pathways mediating cardiovascular aging and developmental programming of cardiovascular disease
title_short Divergence of mechanistic pathways mediating cardiovascular aging and developmental programming of cardiovascular disease
title_sort divergence of mechanistic pathways mediating cardiovascular aging and developmental programming of cardiovascular disease
topic Research Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5036970/
https://www.ncbi.nlm.nih.gov/pubmed/26932929
http://dx.doi.org/10.1096/fj.201500057
work_keys_str_mv AT allisonbethj divergenceofmechanisticpathwaysmediatingcardiovascularaginganddevelopmentalprogrammingofcardiovasculardisease
AT kaandorpjoepej divergenceofmechanisticpathwaysmediatingcardiovascularaginganddevelopmentalprogrammingofcardiovasculardisease
AT kaneandrewd divergenceofmechanisticpathwaysmediatingcardiovascularaginganddevelopmentalprogrammingofcardiovasculardisease
AT cammemilyj divergenceofmechanisticpathwaysmediatingcardiovascularaginganddevelopmentalprogrammingofcardiovasculardisease
AT lusbyciara divergenceofmechanisticpathwaysmediatingcardiovascularaginganddevelopmentalprogrammingofcardiovasculardisease
AT crosschristinem divergenceofmechanisticpathwaysmediatingcardiovascularaginganddevelopmentalprogrammingofcardiovasculardisease
AT nevindolanrhianon divergenceofmechanisticpathwaysmediatingcardiovascularaginganddevelopmentalprogrammingofcardiovasculardisease
AT thakoravneshs divergenceofmechanisticpathwaysmediatingcardiovascularaginganddevelopmentalprogrammingofcardiovasculardisease
AT derksjanb divergenceofmechanisticpathwaysmediatingcardiovascularaginganddevelopmentalprogrammingofcardiovasculardisease
AT tarryadkinsjanel divergenceofmechanisticpathwaysmediatingcardiovascularaginganddevelopmentalprogrammingofcardiovasculardisease
AT ozannesusane divergenceofmechanisticpathwaysmediatingcardiovascularaginganddevelopmentalprogrammingofcardiovasculardisease
AT giussanidinoa divergenceofmechanisticpathwaysmediatingcardiovascularaginganddevelopmentalprogrammingofcardiovasculardisease