Pre-Bötzinger Complex Functions as a Central Hypoxia Chemosensor for Respiration In Vivo
Autor: | Irene C. Solomon, Norman H. Edelman, J. A. Neubauer |
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Rok vydání: | 2000 |
Předmět: |
Periodicity
Microinjections Physiology Pre-Bötzinger complex Vagotomy Membrane Potentials Asphyxia In vivo Sodium Cyanide Respiration medicine Animals Respiratory system Hypoxia Homocysteine chemistry.chemical_classification Medulla Oblongata Chemistry General Neuroscience Respiratory Center Hypoxia (medical) Respiration Artificial Chemoreceptor Cells Cell biology Amino acid Phrenic Nerve Cats Respiratory Physiological Phenomena Excitatory postsynaptic potential medicine.symptom Ionotropic effect |
Zdroj: | Journal of Neurophysiology. 83:2854-2868 |
ISSN: | 1522-1598 0022-3077 |
DOI: | 10.1152/jn.2000.83.5.2854 |
Popis: | Recently, we identified a region located in the pre-Bötzinger complex (pre-BötC; the proposed locus of respiratory rhythm generation) in which activation of ionotropic excitatory amino acid receptors usingdl-homocysteic acid (DLH) elicits a variety of excitatory responses in the phrenic neurogram, ranging from tonic firing to a rapid series of high-amplitude, rapid rate of rise, short-duration inspiratory bursts that are indistinguishable from gasps produced by severe systemic hypoxia. Therefore we hypothesized that this unique region is chemosensitive to hypoxia. To test this hypothesis, we examined the response to unilateral microinjection of sodium cyanide (NaCN) into the pre-BötC in chloralose- or chloralose/urethan-anesthetized vagotomized, paralyzed, mechanically ventilated cats. In all experiments, sites in the pre-BötC were functionally identified using DLH (10 mM, 21 nl) as we have previously described. All sites were histologically confirmed to be in the pre-BötC after completion of the experiment. Unilateral microinjection of NaCN (1 mM, 21 nl) into the pre-BötC produced excitation of phrenic nerve discharge in 49 of the 81 sites examined. This augmentation of inspiratory output exhibited one of the following changes in cycle timing and/or pattern: 1) a series of high-amplitude, short-duration bursts in the phrenic neurogram (a discharge similar to a gasp), 2) a tonic excitation of phrenic neurogram output, 3) augmented bursts in the phrenic neurogram (i.e., eupneic breath ending with a gasplike burst), or 4) an increase in frequency of phrenic bursts accompanied by small increases or decreases in the amplitude of integrated phrenic nerve discharge. Our findings identify a locus in the brain stem in which focal hypoxia augments respiratory output. We propose that the respiratory rhythm generator in the pre-BötC has intrinsic hypoxic chemosensitivity that may play a role in hypoxia-induced gasping. |
Databáze: | OpenAIRE |
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