Increased ventilation and CO2 chemosensitivity in acetylcholinesterase knockout mice

Autor: Eliane Boudinot, Jean Champagnat, Arnaud Chatonnet, Pierre Escourrou, M. J. Emery, Etienne Mouisel, Arthur S. Foutz
Přispěvatelé: Neurobiologie génétique et intégrative (NGI), Centre National de la Recherche Scientifique (CNRS), Institut de Neurobiologie Alfred Fessard (INAF), Sérotonine et neuropharmacologie, Université Paris-Sud - Paris 11 (UP11)-IFR141, Département de Physiologie Animale, Institut National de la Recherche Agronomique (INRA), IFR141-Université Paris-Sud - Paris 11 (UP11), Département de Physiologie Animale (PA), Différenciation Cellulaire et Croissance (DCC), Institut National de la Recherche Agronomique (INRA)-Université Montpellier 2 - Sciences et Techniques (UM2), ProdInra, Migration
Jazyk: angličtina
Rok vydání: 2004
Předmět:
Aging
Mouse
Physiology
[SDV]Life Sciences [q-bio]
MESH: Anoxia
MESH: Carbon Dioxide
MESH: Pulmonary Ventilation
Gene
MESH: Mice
Knockout

Hypercapnia
Mice
0302 clinical medicine
MESH: Aging
MESH: Animals
MESH: Oxygen Consumption
Respiratory system
Hypoxia
ComputingMilieux_MISCELLANEOUS
Mice
Knockout

Mammals
0303 health sciences
Respiration
General Neuroscience
SOURIS KNOCKOUT
Adaptation
Physiological

[SDV] Life Sciences [q-bio]
Acetylcholinesterase
Breathing
MESH: Respiratory Mechanics
Female
CO2
[SDV.NEU]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]
medicine.symptom
Pulmonary and Respiratory Medicine
medicine.medical_specialty
Control of breathing
Respiratory rate
[INFO] Computer Science [cs]
Biology
AChE knockout
03 medical and health sciences
Oxygen Consumption
Internal medicine
MESH: Analysis of Variance
Hyperventilation
medicine
Animals
[INFO]Computer Science [cs]
Chemosensitivity
MESH: Mice
030304 developmental biology
MESH: Respiration
Analysis of Variance
Acetylcholinesterase knockout
Carbon Dioxide
Hypoxia (medical)
MESH: Acetylcholinesterase
MESH: Adaptation
Physiological

Endocrinology
Control of respiration
Enzyme
MESH: Hypercapnia
Respiratory Mechanics
AChE
Pulmonary Ventilation
MESH: Female
030217 neurology & neurosurgery
Zdroj: Respiratory Physiology and Neurobiology
Respiratory Physiology and Neurobiology, Elsevier, 2004, 140 (3), pp.231-41. ⟨10.1016/j.resp.2004.03.002⟩
Respiratory Physiology and Neurobiology, Elsevier, 2004, 140, pp.231-241
ISSN: 1569-9048
1878-1519
DOI: 10.1016/j.resp.2004.03.002⟩
Popis: To investigate the effects of a permanent excess of acetylcholine (AChE) on respiration, breathing and chemosensitivity were analyzed from birth to adulthood in mice lacking the AChE gene (AChE-/-), in heterozygotes, and in control wild-type (AChE+/+) littermates. Breathing at rest and ventilatory responses to brief exposures to hypoxia (10% O2) and hypercapnia (3-5% CO2) were measured by whole-body plethysmography. At rest AChE-/- mice show larger tidal volumes (VT, + 96% in adults), overall ventilation (VE, + 70%), and mean inspiratory flow (+270%) than wild-type mice, with no change in breathing frequency (fR). AChE-/- mice have a slightly blunted response to hypoxia, but increased VE and fR responses to hypercapnia. Heterozygous animals present no consistent alterations of breathing at rest and chemosensitivity is normal. Adult AChE-/- mice have an increased VE/VO2 and a marginally higher normalized VO2. The results suggest that the hyperventilation and altered chemosensitivity in AChE-/- mice largely reflect alterations of central respiratory control.
Databáze: OpenAIRE