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Methods for the development and assessment of atrial fibrillation and heart failure dog models
OBJECTIVE: To report Medtronic experiences with the development of animal models for atrial fibrillation (AF) and chronic heart failure (CHF) using high-rate pacing for AF and microemboli for CHF. METHODS: For the AF model, an atrial lead was attached to a Medtronic Synergy™ neurostimulator, which w...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Science Press
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3390072/ https://www.ncbi.nlm.nih.gov/pubmed/22783299 http://dx.doi.org/10.3724/SP.J.1263.2011.00133 |
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author | Urban, Jon F Gerhart, Renee L Krzeszak, Jason R Leet, Corey R Lentz, Linnea R McClay, Carolyn B |
author_facet | Urban, Jon F Gerhart, Renee L Krzeszak, Jason R Leet, Corey R Lentz, Linnea R McClay, Carolyn B |
author_sort | Urban, Jon F |
collection | PubMed |
description | OBJECTIVE: To report Medtronic experiences with the development of animal models for atrial fibrillation (AF) and chronic heart failure (CHF) using high-rate pacing for AF and microemboli for CHF. METHODS: For the AF model, an atrial lead was attached to a Medtronic Synergy™ neurostimulator, which was programmed to stimulate at 50 Hz in an on-off duty cycle. Atrial natriuretic peptide (ANP), brain natriuretic peptide (BNP) and N-terminal pro brain natriuretic peptide (NT-proBNP) were assayed at select time points. For CHF model, a serial injection of 90 µm polystyrene microspheres at 62,400 beads/mL (Polybead, Polysciences, Inc.) was performed to induce global ischemia, either with weekly monitoring and embolization schedule (group 1, n = 25) or with biweekly monitoring and emboliation schedule (group 2, n = 36 ). Echocardiograms were used along with ventriculograms and magnetic resonance imaging scans weekly to assess cardiac function and ANP, BNP and NT-proBNP were monitored. RESULTS: For the AF model, the days to sustained AF for four animals following surgery were 7, 25, 21 and 19, respectively; For the CHF model, the days to meet CHF endpoints were 116 in group 1 and 89 in group 2. For both AF and CHF models, NT-proBNP correlated well with the development of disease states. CONCLUSION: Our experience for the development and assessment of AF and CHF dog models may help researchers who are in search for animal model for assessing the safety and efficacy of a device-based therapy. |
format | Online Article Text |
id | pubmed-3390072 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Science Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-33900722012-07-10 Methods for the development and assessment of atrial fibrillation and heart failure dog models Urban, Jon F Gerhart, Renee L Krzeszak, Jason R Leet, Corey R Lentz, Linnea R McClay, Carolyn B J Geriatr Cardiol Symposium: Research Articles OBJECTIVE: To report Medtronic experiences with the development of animal models for atrial fibrillation (AF) and chronic heart failure (CHF) using high-rate pacing for AF and microemboli for CHF. METHODS: For the AF model, an atrial lead was attached to a Medtronic Synergy™ neurostimulator, which was programmed to stimulate at 50 Hz in an on-off duty cycle. Atrial natriuretic peptide (ANP), brain natriuretic peptide (BNP) and N-terminal pro brain natriuretic peptide (NT-proBNP) were assayed at select time points. For CHF model, a serial injection of 90 µm polystyrene microspheres at 62,400 beads/mL (Polybead, Polysciences, Inc.) was performed to induce global ischemia, either with weekly monitoring and embolization schedule (group 1, n = 25) or with biweekly monitoring and emboliation schedule (group 2, n = 36 ). Echocardiograms were used along with ventriculograms and magnetic resonance imaging scans weekly to assess cardiac function and ANP, BNP and NT-proBNP were monitored. RESULTS: For the AF model, the days to sustained AF for four animals following surgery were 7, 25, 21 and 19, respectively; For the CHF model, the days to meet CHF endpoints were 116 in group 1 and 89 in group 2. For both AF and CHF models, NT-proBNP correlated well with the development of disease states. CONCLUSION: Our experience for the development and assessment of AF and CHF dog models may help researchers who are in search for animal model for assessing the safety and efficacy of a device-based therapy. Science Press 2011-09 /pmc/articles/PMC3390072/ /pubmed/22783299 http://dx.doi.org/10.3724/SP.J.1263.2011.00133 Text en Institute of Geriatric Cardiology http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License, which allows readers to alter, transform, or build upon the article and then distribute the resulting work under the same or similar license to this one. The work must be attributed back to the original author and commercial use is not permitted without specific permission. |
spellingShingle | Symposium: Research Articles Urban, Jon F Gerhart, Renee L Krzeszak, Jason R Leet, Corey R Lentz, Linnea R McClay, Carolyn B Methods for the development and assessment of atrial fibrillation and heart failure dog models |
title | Methods for the development and assessment of atrial fibrillation and heart failure dog models |
title_full | Methods for the development and assessment of atrial fibrillation and heart failure dog models |
title_fullStr | Methods for the development and assessment of atrial fibrillation and heart failure dog models |
title_full_unstemmed | Methods for the development and assessment of atrial fibrillation and heart failure dog models |
title_short | Methods for the development and assessment of atrial fibrillation and heart failure dog models |
title_sort | methods for the development and assessment of atrial fibrillation and heart failure dog models |
topic | Symposium: Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3390072/ https://www.ncbi.nlm.nih.gov/pubmed/22783299 http://dx.doi.org/10.3724/SP.J.1263.2011.00133 |
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