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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Federation of American Societies for Experimental Biology
2016
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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 |
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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 |
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