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1 Department of Physiology and Biophysics, College of Medicine Howard University and Specialized Neuroscience Research Program of Howard University, Washington, DC 20059; Departments of 2 Anatomy, 3 Neuroscience, 4 Pediatrics, and 5 Psychiatry, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106
In this study, we examined effects of
chemical stimulation of the ventrolateral region of the midbrain
periaqueductal gray (vl PAG) on airway smooth muscle tone. We observed
that in anesthetized, paralyzed, and artificially ventilated ferrets,
vl PAG stimulation elicited airway smooth muscle relaxation. To clarify
the mechanisms underlying this observation, we examined the
GABA-GABAA receptor signaling pathway by 1)
examining the expression of GABAA receptors on
airway-related vagal preganglionic neurons (AVPNs) located in the
rostral nucleus ambiguus region (rNA), by use of receptor immunochemistry and confocal microscopy; 2) measuring GABA
release within the rNA by using microdialysis; and 3)
performing physiological experiments to determine the effects of
selective blockade of GABAA receptors expressed by AVPNs in
the rNA region on vl PAG-induced airway relaxation, thereby defining
the role of the GABAA receptor subtype in this process. We
observed that AVPNs located in the rNA region do express the
GABAA receptor
-subtype. In addition, we demonstrated
that activation of vl PAG induced GABA release within the rNA region,
and this release was associated with airway smooth muscle relaxation.
Blockade of the GABAA receptor subtype expressed by AVPNs
in the rNA by bicuculline diminished the inhibitory effects of vl PAG
stimulation on airway smooth muscle tone. These data indicate, for the
first time, that activation of vl PAG dilates the airways by a release
of GABA and activation of GABAA receptors expressed by AVPNs.
central control of airway smooth muscle tone; airway dilation; ventrolateral periaqueductal gray; nucleus ambiguus; airway-related vagal preganglionic neurons; parasympathetic nervous system; microdialysis; GABA; GABAA receptors; bicuculline
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