The lateral cell columns of the midbrain periaqueductal gray (PAG) constitute a major anatomical link between hypothalamic regions implicated in sleep-wake control and respiratory control sites within the medulla. Stimulation of the PAG can alter respiration and neurons with respiratory- related discharge have been identified within the PAG of primates and cats. We hypothesize that hypothalamic sleep-wake control mechanisms modulate medullary respiratory control systems, in part, via effects on PAG neurons. Specifically, we hypothesize that gamma-aminobutyric acid (GABA)- containing neurons from the preoptic anterior hypothalamic area (POA) exert inhibitory effects on respiratory-related PAG neurons during non-REM sleep. We have previously demonstrated that thermosensitive neurons are a critical component of the POA sleep control mechanism, and we hypothesize that focal POA warming will enhance GABA-mediated inhibition of PAG respiratory-related activity. To test these hypotheses, we will: 1) document the extent of the direct GABAergic projection from the POA to the PAG in rats and cats; 2) determine the ability of PAG micro-infusions to suppress breathing and upper airway muscle activity in rat and cats during waking and sleep; 3) document the state dependency of respiratory-related neuronal activity within the lateral PAG cell columns using chronic micro-wire recording techniques, and determine whether or not changes observed in on-REM sleep are similar to those evoked by mild hypothalamic warning; 4) attempt to prevent non-REM sleep-related and POA-warming induced changes in PAG neuronal activity by concurrently delivering GABA-receptor antagonists to PAG micro-wire recording sites via an adjacent microdialysis probe. Proposed studies will be the first to directly examine the involvement of extensive POA>PAG> medullary pathways in state-dependent respiratory control. They will help to characterize the functional neuroanatomy and the neuropharmacology of normal and disordered breathing during sleep.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Specialized Center (P50)
Project #
5P50HL060296-04
Application #
6505106
Study Section
Project Start
2001-09-01
Project End
2002-08-31
Budget Start
Budget End
Support Year
4
Fiscal Year
2001
Total Cost
$266,631
Indirect Cost
Name
University of California Los Angeles
Department
Type
DUNS #
119132785
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
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