Skip to main content

Cooperativity in Distributed Respiratory and Cardiovascular-Related Brainstem Neural Assemblies: Insights from Many-Neuron Recordings

  • Conference paper
Cardiorespiratory and Motor Coordination

Abstract

Baroreceptor stimulation causes a decline in respiratory frequency and tidal volume [16]. The brainstem mechanisms that mediate these changes are not well understood [2, 3, 16]. Neurons distributed in the nucleus tractus solitarius and both midline and ventrolateral regions of the medulla have been implicated in the regulation of breathing and cardiovascular control [1–5, 12, 13, 15, 18]. Our working hypothesis is that the bulbospinal projections that control the muscles of breathing and the sympathetic innervation of the cardiovascular system are regulated by a shared, dynamically organized, distributed neural network. The study of emergent network properties and processes requires the ability to represent the state (e.g., degree of synchrony) of subsets of neural assemblies as they interact. Traditional methods lack the spatial and temporal resolution needed for this task. In this preliminary report, we describe the use of many-neuron recordings and quantitative analytical methods to detect and evaluate functional connectivity and cooperative behavior among brainstem cardiorespiratory neurons. The data obtained with this approach support the hypothesis that a distributed neural network in the midline of the medulla contributes to both the stability of the breathing pattern and to changes in that pattern associated with altered baroreceptor activity.

This research was supported by NIH grant NS 19814.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 84.99
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 109.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. Barman SM, Gebber GL (1989) Lateral tegmental field neurons of the cat medulla: a source of basel activity of raphespinal Sympathoinhibitory neurons. J Neurophysiol 61: 1011–1024

    PubMed  CAS  Google Scholar 

  2. Ciriello J, Caverson MM, Polosa C (1986) Function of the ventrolateral medulla in the control of the circulation. Brain Res Rev 11: 359–391

    Article  Google Scholar 

  3. Feldman JL, Ellenberger HH (1988) Central coordination of respiratory and cardiovascular control in mammals. Annu Rev Physiol 50: 593–606

    Article  PubMed  CAS  Google Scholar 

  4. Holtman JR Jr, Dick TE, Berger AJ (1986) Involvement of serotonin in the excitation of phrenic motoneurons evoked by stimulation of the raphe obscurus. J Neurosci 6: 1185–1193

    PubMed  Google Scholar 

  5. Lalley PM (1986) Serotoninergic and non-serotoninergic responses of phrenic motoneurones to raphe stimulation in the cat. J Physiol (Lond) 380: 373–385

    CAS  Google Scholar 

  6. Lindsey BG, Hernandez Y, Shannon R (1989) Functional connectivity among respiratory related midline medullary neurons. Proc Int Union Physiol Sci 27: 305

    Google Scholar 

  7. Lindsey BG, Hernandez YM, Shannon R, Gerstein GL (1989) Respiratory and cardiac related brainstem neural assemblies• dynamic functional connectivity. Soc Neurosci Abst 15: 1191

    Google Scholar 

  8. Lindsey BG, Segers LS, Shannon R (1987) Functional associations among simultaneously monitored lateral medullary respiratory neurons in the cat. II. Evidence for inhibitory actions of expiratory neurons. J Neurophysiol 57: 1101–1117

    Google Scholar 

  9. Lindsey BG, Segers LS, Shannon R (1987) Functional associations of ventral respiratory group neurons with midline and contralateral respiratory-modulated brainstem neurons. Soc Neurosci Abst 13: 1586

    Google Scholar 

  10. Lindsey BG, Segers LS, Shannon R (1989) Discharge patterns of rostrolateral medullary expiratory neurons in the cat: regulation by concurrent network processes. J Neurophysiol 61: 1185–1196

    PubMed  CAS  Google Scholar 

  11. Lindsey BG, Shannon R, Gerstein GL (1989) Gravitational representation of simultaneously recorded brainstem respiratory neuron spike trains. Brain Res 483: 373–378

    Article  PubMed  CAS  Google Scholar 

  12. McAllen RM (1987) Central respiratory modulation of subretrofacial bulbospinal neurons in the cat. J Physiol (Lond) 388: 533–545

    CAS  Google Scholar 

  13. Millhorn DE (1986) Stimulation of raphe (obscurus) nucleus causes long-term potentiation of phrenic nerve activity in cat. J Physiol (Lond) 381: 169–179

    CAS  Google Scholar 

  14. Millhorn DE, Hokfelt T (1988) Chemical messengers and their coexistence in individual neurons. NIPS 3: 1–5

    CAS  Google Scholar 

  15. Morrison SF, Gebber GL (1984) Raphe neurons with sympathetic-related activity: baroreceptor responses and spinal connections. Am J Physiol 246: R338 - R348

    PubMed  CAS  Google Scholar 

  16. Nishino T, Honda Y (1982) Changes in pattern of breathing following baroreceptor stimulation in cats. Japn J Physiol 32: 183–195

    Article  CAS  Google Scholar 

  17. Remmers JE, Richter DW, Ballantyne D, Bainton CR, Klein JP (1986) Reflex prolongation of stage I of expiration. Pflugers Arch 407: 190–198

    Article  PubMed  CAS  Google Scholar 

  18. Richter DW, Seller H (1975) Baroreceptor effects on medullary respiratory neurones of the cat. Brain Res 86: 168–171

    Article  PubMed  CAS  Google Scholar 

  19. Segers LS, Shannon R, Saporta S, Lindsey BG (1987) Functional associations among simultaneously monitored lateral medullary respiratory neurons in the cat. I. Evidence for excitatory and inhibitory actions of inspiratory neurons. J Neurophysiol 57: 1078–1100

    Google Scholar 

Download references

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 1991 Springer-Verlag Berlin Heidelberg

About this paper

Cite this paper

Lindsey, B.G., Hernandez, Y.M., Shannon, R. (1991). Cooperativity in Distributed Respiratory and Cardiovascular-Related Brainstem Neural Assemblies: Insights from Many-Neuron Recordings. In: Koepchen, HP., Huopaniemi, T. (eds) Cardiorespiratory and Motor Coordination. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-75507-1_15

Download citation

  • DOI: https://doi.org/10.1007/978-3-642-75507-1_15

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-540-52279-9

  • Online ISBN: 978-3-642-75507-1

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics