Volume 2 Supplement 1

Neural Control of Breathing

Open Access

Mechanisms of respiratory rhythm generation in vitro. I. Pacemaker neurons and networks in the pre-Bötzinger complex (pre-BötC)

  • JC Smith1,
  • N Koshiya1, 2,
  • CA Del Negro1,
  • RJ Butera3 and
  • CG Wilson1
Respiratory Research20012(Suppl 1):2.5

https://doi.org/10.1186/rr99

Received: 2 August 2001

Published: 17 August 2001

We have proposed that the inspiratory rhythm-generating kernel in the pre-BötC consists of a heterogeneous network of glutamatergic neurons with voltage-dependent pacemaker-like bursting properties. This model is based on our optical imaging [1], electrophysiological [2], and mathematical modeling [3] studies of inspiratory (I) neurons within the pre-BötC of rhythmically active in vitro transverse slice preparations from neonatal rats. For electrophysiological and imaging studies, we have developed novel methods to optically identify I neurons with Ca2+-sensitive dyes combined with IR-DIC imaging for whole-cell current camp (CC) and voltage clamp (VC) analyses of neuronal membrane conductance and synaptic mechanisms. In computational modeling studies we have developed models of single pacemaker neurons and synaptically-coupled networks of these neurons (50–500 cells) with heterogeneous distributions of cellular/network parameters. Model predictions have been tested experimentally from single-cell electrophysiological measurements and from macroscopic recordings of neuron population activity within the pre-BötC [2].

Electrophysiological and optical measurements demonstrate a sub-population of pre-BötC I neurons that exhibit voltage-dependent rhythmic bursting under CC after blockade of non-NMDA gluta-matergic synaptic transmission or after blocking synaptic transmission with Ca2+ channel blockers. The intrinsic bursting frequency of these pacemaker-type cells was a monotonic function of baseline membrane potential, spanning a frequency range of over an order of magnitude (~0.05–1 Hz); the voltage-dependence and frequency range varied for different cells indicating heterogeneity. Under VC with synaptic transmission intact, these pacemaker neurons exhibited glutamatergic synaptic drive currents. Optical imaging and cross-correlation of rhythmic Ca2+ activities of multiple cells demonstrate that the glutamatergic synaptic interactions synchronize bursting within the heterogeneous population, but with a temporal dispersion in neuronal spiking including pre-I spiking patterns [2,3]. Measurements of pre-BötC population activity show network frequency control by changing pre-BötC excitability, like predictions from our network models [3].

We have obtained evidence that a persistent Na+ current (INaP) is the main subthreshold-activating cationic conductance underlying the voltage-dependent pacemaker bursting. We measured Na+ currents in bursting pacemaker and non-bursting pre-BötC I cells. In all cells tested under VC, voltage ramp commands at rates of <100 mV/s inactivated the fast Na+ current and yielded N-shaped IV curves with a negative slope region between -60 and -35 mV. TTX (1 μM) blocked this inward current. The slowest ramp speed tested (3.3 mV/s) failed to fully inactivate the negative slope generating current. The current is therefore a TTX-sensitive INaP. The peak amplitude of INaP ranged from -50 to -100 pA at Em = -20 mV (peak conductance = ~1–2 nS). Boltzmann plots gave half-maximal activation voltage of ~-40 mV and a slope factor of ~5, very similar to values used for INaP in our pacemaker neuron models [3]. In non-pacemaker Icells, the ratio of INaP/Ileak was insufficient to support intrinsic bursting as predicted by our models. Further tests of the role of INaP have been performed using the dynamic clamp to artificially add INaP to non-pacemaker neurons. INaP transformed these neurons into rhythmic bursters with voltage-dependent behavior quantitatively similar to our models and experimental observations.

These results generally support our conceptual and computational models for the rhythm-generation kernel as a heterogeneous pacemaker network.

Authors’ Affiliations

(1)
Laboratory of Neural Control, NINDS, NIH
(2)
Blanchette Rockefeller Neurosciences Institute, Johns Hopkins University
(3)
Laboratory for Neuroengineering, Georgia Tech

References

  1. Koshiya N, Smith JC: Neuronal pacemaker for breathing visualized in vitro. Nature. 1999, 400: 360-363. 10.1038/22540.PubMedView ArticleGoogle Scholar
  2. Del Negro CA, Johnson SM, Butera RJ, Smith JC: Models of respiratory rhythm generation in the pre-botzinger complex. iii. experimental tests of model predictions. J Neurophysiol. 2001, 86: 59-74.PubMedGoogle Scholar
  3. Butera RJ, Rinzel J, Smith JC: Models of respiratory rhythm generation in the pre-Botzinger complex. I. Bursting pacemaker neurons. J Neurophysiol. 1999, 81: 382-397.Google Scholar
  4. Butera RJ, Rinzel J, Smith JC: Models of respiratory rhythm generation in the pre-Botzinger complex. II. Populations Of coupled pacemaker neurons. J Neurophysiol. 1999, 81: 398-415.Google Scholar

Copyright

© BioMed Central Ltd 2001

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