Postnatal Intermittent Hypoxia and Respiration: Potenti*
Project Number5F30NS048770-03
Former Number1F31NS048770-01A1
Contact PI/Project LeaderREEVES, STEPHEN R
Awardee OrganizationUNIVERSITY OF LOUISVILLE
Description
Abstract Text
DESCRIPTION (provided by applicant): Intermittent hypoxia (IH) is a frequent condition in clinical medicine (e.g., sleep apnea, SIDS), which bears substantial morbidity and mortality. Furthermore, organismal adaptations to IH suggest the formation of specific forms of neuronal plasticity. While substantial study of the effects of IH has been performed in the mature mammal, little if any work has been done during the early phases of post-natal development, a unique period of neuronal vulnerability and adaptation. Therefore, we hypothesized that post-natal intermittent hypoxia, such as occurs in sleep apnea, may impose long-term modifications in respiratory control, thereby leading to a form of metaplasticity of respiratory patterning. The latter modification of the respiratory network induced by early post-natal IH could impose either a functionally favorable or a maladaptive alteration of the respiratory response system. To examine this issue, we will: (i) characterize the effects of post-natal IH on normoxic ventilation and on hypoxic and hypercapnic ventilatory responses in freely behaving rats.; (ii) assess the effects of IH on phrenic motor nerve long-term facilitation (LTF).; (iii) determine the potential role of signaling pathways, particularly protein kinase C (PKC), in the long-term modification of ventilation imposed by IH through development. This work will therefore contribute to the understanding of potential mechanisms mediating not only early adaptations to IH but also provide insights to long-lasting changes in ventilation that may develop when a conditioning stimulus is applied during critical phase of maturation.
Public Health Relevance Statement
Data not available.
NIH Spending Category
No NIH Spending Category available.
Project Terms
Clinical MedicineConditionDevelopmentEnvironmental air flowHypoxiaMammalsMediatingModificationMorbidity - disease rateMotorNerveNeuronal PlasticityNeuronsPathway interactionsPatternPhaseProtein Kinase CRattusRespirationRoleSignal PathwaySleep Apnea SyndromesStimulusStructure of phrenic nerveSudden infant death syndromeSystemUrsidae FamilyWorkawakeconditioninginsightmortalitypost-natal intermittent hypoxiapostnatalrespiratoryresponse
National Institute of Neurological Disorders and Stroke
CFDA Code
853
DUNS Number
057588857
UEI
E1KJM4T54MK6
Project Start Date
01-July-2005
Project End Date
30-June-2008
Budget Start Date
01-July-2007
Budget End Date
30-June-2008
Project Funding Information for 2007
Total Funding
$33,184
Direct Costs
$33,184
Indirect Costs
Year
Funding IC
FY Total Cost by IC
2007
National Institute of Neurological Disorders and Stroke
$33,184
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 5F30NS048770-03
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