Cardiovascular response to beta-adrenergic blockade or activation in 23 inbred mouse strains

Berthonneche, Corinne; Peter, Bastian; Schüpfer, Fanny; Hayoz, Pamela; Kutalik, Zoltán; Abriel, Hugues; Pedrazzini, Thierry; Beckmann, Jacques S; Bergmann, Sven; Maurer, Fabienne (2009). Cardiovascular response to beta-adrenergic blockade or activation in 23 inbred mouse strains. PLoS ONE, 4(8), e6610. Lawrence, Kans.: Public Library of Science 10.1371/journal.pone.0006610

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We report the characterisation of 27 cardiovascular-related traits in 23 inbred mouse strains. Mice were phenotyped either in response to chronic administration of a single dose of the beta-adrenergic receptor blocker atenolol or under a low and a high dose of the beta-agonist isoproterenol and compared to baseline condition. The robustness of our data is supported by high trait heritabilities (typically H(2)>0.7) and significant correlations of trait values measured in baseline condition with independent multistrain datasets of the Mouse Phenome Database. We then focused on the drug-, dose-, and strain-specific responses to beta-stimulation and beta-blockade of a selection of traits including heart rate, systolic blood pressure, cardiac weight indices, ECG parameters and body weight. Because of the wealth of data accumulated, we applied integrative analyses such as comprehensive bi-clustering to investigate the structure of the response across the different phenotypes, strains and experimental conditions. Information extracted from these analyses is discussed in terms of novelty and biological implications. For example, we observe that traits related to ventricular weight in most strains respond only to the high dose of isoproterenol, while heart rate and atrial weight are already affected by the low dose. Finally, we observe little concordance between strain similarity based on the phenotypes and genotypic relatedness computed from genomic SNP profiles. This indicates that cardiovascular phenotypes are unlikely to segregate according to global phylogeny, but rather be governed by smaller, local differences in the genetic architecture of the various strains.

Item Type:

Journal Article (Original Article)

Division/Institute:

04 Faculty of Medicine > Pre-clinic Human Medicine > BioMedical Research (DBMR) > DBMR Forschung Mu35 > Forschungsgruppe Ionenkanalkrankheiten
04 Faculty of Medicine > Pre-clinic Human Medicine > BioMedical Research (DBMR) > DBMR Forschung Mu35 > Forschungsgruppe Ionenkanalkrankheiten

UniBE Contributor:

Abriel, Hugues

ISSN:

1932-6203

Publisher:

Public Library of Science

Language:

English

Submitter:

Factscience Import

Date Deposited:

04 Oct 2013 15:10

Last Modified:

05 Aug 2016 15:01

Publisher DOI:

10.1371/journal.pone.0006610

PubMed ID:

19672458

Web of Science ID:

000268935900021

BORIS DOI:

10.7892/boris.30836

URI:

https://boris.unibe.ch/id/eprint/30836 (FactScience: 195165)

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