Affiliation:
1. New Jersey Institute of Technology and Rutgers University, Newark, New Jersey;
2. Seattle Children's Research Institute, Center for Integrative Brain Research; and
3. Department of Neurological Surgery, University of Washington, Seattle, Washington
Abstract
Neurons depend on aerobic metabolism, yet are very sensitive to oxidative stress and, as a consequence, typically operate in a low O2 environment. The balance between blood flow and metabolic activity, both of which can vary spatially and dynamically, suggests that local O2 availability markedly influences network output. Yet the understanding of the underlying O2-sensing mechanisms is limited. Are network responses regulated by discrete O2-sensing mechanisms or, rather, are they the consequence of inherent O2 sensitivities of mechanisms that generate the network activity? We hypothesized that a broad range of O2 tensions progressively modulates network activity of the pre-Bötzinger complex (preBötC), a neuronal network critical to the central control of breathing. Rhythmogenesis was measured from the preBötC in transverse neonatal mouse brain stem slices that were exposed to graded reductions in O2 between 0 and 95% O2, producing tissue oxygenation values ranging from 20 ± 18 (mean ± SE) to 440 ± 56 Torr at the slice surface, respectively. The response of the preBötC to graded changes in O2 is progressive for some metrics and abrupt for others, suggesting that different aspects of the respiratory network have different sensitivities to O2.
Publisher
American Physiological Society
Subject
Physiology,General Neuroscience
Cited by
40 articles.
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