Literature DB >> 35380537

Putting the theory into 'burstlet theory' with a biophysical model of burstlets and bursts in the respiratory preBötzinger complex.

Ryan S Phillips1, Jonathan E Rubin1.   

Abstract

Inspiratory breathing rhythms arise from synchronized neuronal activity in a bilaterally distributed brainstem structure known as the preBötzinger complex (preBötC). In in vitro slice preparations containing the preBötC, extracellular potassium must be elevated above physiological levels (to 7-9 mM) to observe regular rhythmic respiratory motor output in the hypoglossal nerve to which the preBötC projects. Reexamination of how extracellular K+ affects preBötC neuronal activity has revealed that low-amplitude oscillations persist at physiological levels. These oscillatory events are subthreshold from the standpoint of transmission to motor output and are dubbed burstlets. Burstlets arise from synchronized neural activity in a rhythmogenic neuronal subpopulation within the preBötC that in some instances may fail to recruit the larger network events, or bursts, required to generate motor output. The fraction of subthreshold preBötC oscillatory events (burstlet fraction) decreases sigmoidally with increasing extracellular potassium. These observations underlie the burstlet theory of respiratory rhythm generation. Experimental and computational studies have suggested that recruitment of the non-rhythmogenic component of the preBötC population requires intracellular Ca2+ dynamics and activation of a calcium-activated nonselective cationic current. In this computational study, we show how intracellular calcium dynamics driven by synaptically triggered Ca2+ influx as well as Ca2+ release/uptake by the endoplasmic reticulum in conjunction with a calcium-activated nonselective cationic current can reproduce and offer an explanation for many of the key properties associated with the burstlet theory of respiratory rhythm generation. Altogether, our modeling work provides a mechanistic basis that can unify a wide range of experimental findings on rhythm generation and motor output recruitment in the preBötC.
© 2022, Phillips and Rubin.

Entities:  

Keywords:  burstlets; calcium induced calcium release; central pattern generator; computational biology; computational model; mouse; neuroscience; rat; respiration; rhythm generation; systems biology

Mesh:

Substances:

Year:  2022        PMID: 35380537      PMCID: PMC9023056          DOI: 10.7554/eLife.75713

Source DB:  PubMed          Journal:  Elife        ISSN: 2050-084X            Impact factor:   8.713


  73 in total

1.  Role of persistent sodium current in mouse preBötzinger Complex neurons and respiratory rhythm generation.

Authors:  Ryland W Pace; Devin D Mackay; Jack L Feldman; Christopher A Del Negro
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2.  Periodicity, mixed-mode oscillations, and quasiperiodicity in a rhythm-generating neural network.

Authors:  Christopher A Del Negro; Christopher G Wilson; Robert J Butera; Henrique Rigatto; Jeffrey C Smith
Journal:  Biophys J       Date:  2002-01       Impact factor: 4.033

3.  Primary structure and functional expression of a rat G-protein-coupled muscarinic potassium channel.

Authors:  Y Kubo; E Reuveny; P A Slesinger; Y N Jan; L Y Jan
Journal:  Nature       Date:  1993-08-26       Impact factor: 49.962

4.  Two types of independent bursting mechanisms in inspiratory neurons: an integrative model.

Authors:  Natalia Toporikova; Robert J Butera
Journal:  J Comput Neurosci       Date:  2010-09-14       Impact factor: 1.621

Review 5.  Ryanodine receptors: structure, expression, molecular details, and function in calcium release.

Authors:  Johanna T Lanner; Dimitra K Georgiou; Aditya D Joshi; Susan L Hamilton
Journal:  Cold Spring Harb Perspect Biol       Date:  2010-10-20       Impact factor: 10.005

6.  Emergence of population bursts from simultaneous activation of small subsets of preBötzinger complex inspiratory neurons.

Authors:  Kaiwen Kam; Jason W Worrell; Cathie Ventalon; Valentina Emiliani; Jack L Feldman
Journal:  J Neurosci       Date:  2013-02-20       Impact factor: 6.167

7.  Defining preBötzinger Complex Rhythm- and Pattern-Generating Neural Microcircuits In Vivo.

Authors:  Yan Cui; Kaiwen Kam; David Sherman; Wiktor A Janczewski; Yu Zheng; Jack L Feldman
Journal:  Neuron       Date:  2016-08-03       Impact factor: 17.173

8.  Somatic Ca2+ transients do not contribute to inspiratory drive in preBötzinger Complex neurons.

Authors:  Consuelo Morgado-Valle; Luis Beltran-Parrazal; Marino DiFranco; Julio L Vergara; Jack L Feldman
Journal:  J Physiol       Date:  2008-07-17       Impact factor: 5.182

9.  Testing the hypothesis of neurodegeneracy in respiratory network function with a priori transected arterially perfused brain stem preparation of rat.

Authors:  Sarah E Jones; Mathias Dutschmann
Journal:  J Neurophysiol       Date:  2016-02-17       Impact factor: 2.714

10.  Evaluating the Burstlet Theory of Inspiratory Rhythm and Pattern Generation.

Authors:  Prajkta S Kallurkar; Cameron Grover; Maria Cristina D Picardo; Christopher A Del Negro
Journal:  eNeuro       Date:  2020-01-15
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  2 in total

1.  Inspiratory rhythm generation is stabilized by Ih.

Authors:  Nicholas J Burgraff; Ryan S Phillips; Liza J Severs; Nicholas E Bush; Nathan A Baertsch; Jan-Marino Ramirez
Journal:  J Neurophysiol       Date:  2022-06-08       Impact factor: 2.974

2.  Predictions and experimental tests of a new biophysical model of the mammalian respiratory oscillator.

Authors:  Ryan S Phillips; Hidehiko Koizumi; Yaroslav I Molkov; Jonathan E Rubin; Jeffrey C Smith
Journal:  Elife       Date:  2022-07-07       Impact factor: 8.713

  2 in total

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