Literature DB >> 23290341

Ventilatory pattern and energy expenditure are altered in cystic fibrosis mice.

Rebecca J Darrah1, Ilya R Bederman, Anna L Mitchell, Craig A Hodges, Cara K Campanaro, Mitchell L Drumm, Frank J Jacono.   

Abstract

BACKGROUND: Altered ventilatory pattern and increased energy expenditure are facets of the complex cystic fibrosis (CF) phenotype. It is not known whether these are inherent attributes of CF, secondary consequences of lung infection or other disease complications.
METHODS: Studies were performed in congenic C57BL/6J, F508del (Cftr((tm1kth))) and CF gut-corrected (F508del) mice. Ventilatory patterns were measured using whole-body plethysmography. Indirect calorimetry was used to determine oxygen consumption, carbon dioxide production and resting energy expenditure.
RESULTS: CF mice (F508del and F508del gut-corrected) have a significantly faster respiratory rate and increased ventilatory pattern variability as compared to non-CF mice. F508del but not CF gut-corrected mice had significantly increased energy expenditure per gram body weight.
CONCLUSIONS: CF mice exhibit a faster, more variable ventilatory pattern. These changes were present in the absence of detectable infection or illness due to gastrointestinal obstruction. Increased resting energy expenditure does not completely account for these differences.
Copyright © 2012 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.

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Year:  2013        PMID: 23290341      PMCID: PMC3620718          DOI: 10.1016/j.jcf.2012.11.008

Source DB:  PubMed          Journal:  J Cyst Fibros        ISSN: 1569-1993            Impact factor:   5.482


  33 in total

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2.  Ventilatory behavior during sleep among A/J and C57BL/6J mouse strains.

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Authors:  J E Marcotte; R K Grisdale; H Levison; A L Coates; G J Canny
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5.  Resting energy expenditure and substrate oxidation rates in cystic fibrosis.

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Journal:  Arch Dis Child       Date:  1993-06       Impact factor: 3.791

6.  Ventilatory responses to hypercapnia and hypoxia in conscious cystic fibrosis knockout mice Cftr-/-.

Authors:  Monique Bonora; Jean-Francois Bernaudin; Claude Guernier; Marie Christiane Brahimi-Horn
Journal:  Pediatr Res       Date:  2004-02-05       Impact factor: 3.756

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Journal:  Chest       Date:  1992-10       Impact factor: 9.410

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Authors:  Peter R Durie; Geraldine Kent; M James Phillips; Cameron A Ackerley
Journal:  Am J Pathol       Date:  2004-04       Impact factor: 4.307

9.  Correction of lethal intestinal defect in a mouse model of cystic fibrosis by human CFTR.

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Journal:  Science       Date:  1994-12-09       Impact factor: 47.728

10.  The "Goldilocks effect" in cystic fibrosis: identification of a lung phenotype in the cftr knockout and heterozygous mouse.

Authors:  J Craig Cohen; Lennart K A Lundblad; Jason H T Bates; Michael Levitzky; Janet E Larson
Journal:  BMC Genet       Date:  2004-07-27       Impact factor: 2.797

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  9 in total

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Authors:  Ilya R Bederman; Gavriella Pora; Maureen O'Reilly; James Poleman; Kimberly Spoonhower; Michelle Puchowicz; Aura Perez; Bernadette O Erokwu; Alex Rodriguez-Palacios; Chris A Flask; Mitchell L Drumm
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2018-08-17       Impact factor: 4.052

2.  Subacute TGFβ Exposure Drives Airway Hyperresponsiveness in Cystic Fibrosis Mice through the PI3K Pathway.

Authors:  Elizabeth L Kramer; Satish K Madala; Kristin M Hudock; Cynthia Davidson; John P Clancy
Journal:  Am J Respir Cell Mol Biol       Date:  2020-05       Impact factor: 6.914

3.  Subacute TGFβ expression drives inflammation, goblet cell hyperplasia, and pulmonary function abnormalities in mice with effects dependent on CFTR function.

Authors:  Elizabeth L Kramer; William D Hardie; Satish K Madala; Cynthia Davidson; John P Clancy
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2018-06-07       Impact factor: 5.464

4.  AGTR2 absence or antagonism prevents cystic fibrosis pulmonary manifestations.

Authors:  Rebecca J Darrah; Frank J Jacono; Neha Joshi; Anna L Mitchell; Abdus Sattar; Cara K Campanaro; Paul Litman; Jennifer Frey; David E Nethery; Eric S Barbato; Craig A Hodges; Harriet Corvol; Garry R Cutting; Michael R Knowles; Lisa J Strug; Mitchell L Drumm
Journal:  J Cyst Fibros       Date:  2018-06-22       Impact factor: 5.482

5.  plethy: management of whole body plethysmography data in R.

Authors:  Daniel Bottomly; Beth Wilmot; Shannon K McWeeney
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6.  Dysregulation of Circadian Rhythm Gene Expression in Cystic Fibrosis Mice.

Authors:  Eric Barbato; Hannah Mianzo; Paul Litman; Rebecca Darrah
Journal:  J Circadian Rhythms       Date:  2019-04-18

Review 7.  Airway disease phenotypes in animal models of cystic fibrosis.

Authors:  Alexandra McCarron; Martin Donnelley; David Parsons
Journal:  Respir Res       Date:  2018-04-02

8.  Cystic Fibrosis Mice Develop Spontaneous Chronic Bordetella Airway Infections.

Authors:  R Darrah; T Bonfield; J J LiPuma; P Litman; C A Hodges; F Jacono; M Drumm
Journal:  J Infect Pulm Dis       Date:  2017-11-02

9.  Alleviation of depression-like behavior in a cystic fibrosis mouse model by Hdac6 depletion.

Authors:  Deborah A Corey; Sharon M Rymut; Thomas J Kelley
Journal:  Sci Rep       Date:  2020-10-01       Impact factor: 4.379

  9 in total

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