Computational model of bladder small DRG neuron soma (Mandge & Manchanda 2018)

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Accession:243448
Bladder small DRG neurons, which are putative nociceptors pivotal to urinary bladder function, express more than a dozen different ionic membrane mechanisms: ion channels, pumps and exchangers. Small-conductance Ca2+-activated K+ (SKCa) channels which were earlier thought to be gated solely by intracellular Ca2+ concentration ([Ca]i ) have recently been shown to exhibit inward rectification with respect to membrane potential. The effect of SKCa inward rectification on the excitability of these neurons is unknown. Furthermore, studies on the role of KCa channels in repetitive firing and their contributions to different types of afterhyperpolarization (AHP) in these neurons are lacking. In order to study these phenomena, we first constructed and validated a biophysically detailed single compartment model of bladder small DRG soma constrained by physiological data. The model includes twenty-two major known membrane mechanisms along with intracellular Ca2+ dynamics comprising Ca2+ diffusion, cytoplasmic buffering, and endoplasmic reticulum (ER) and mitochondrial mechanisms. Using modelling studies, we show that inward rectification of SKCa is an important parameter regulating neuronal repetitive firing and that its absence reduces action potential (AP) firing frequency. We also show that SKCa is more potent in reducing AP spiking than the large-conductance KCa channel (BKCa) in these neurons. Moreover, BKCa was found to contribute to the fast AHP (fAHP) and SKCa to the medium-duration (mAHP) and slow AHP (sAHP). We also report that the slow inactivating A-type K+ channel (slow KA) current in these neurons is composed of 2 components: an initial fast inactivating (time constant ~ 25-100 ms) and a slow inactivating (time constant ~ 200-800 ms) current. We discuss the implications of our findings, and how our detailed model can help further our understanding of the role of C-fibre afferents in the physiology of urinary bladder as well as in certain disorders.
Reference:
1 . Mandge D, Manchanda R (2018) A biophysically detailed computational model of urinary bladder small DRG neuron soma PLOS Computational Biology [PubMed]
Model Information (Click on a link to find other models with that property)
Model Type: Neuron or other electrically excitable cell;
Brain Region(s)/Organism:
Cell Type(s): Dorsal Root Ganglion (DRG) cell; Urinary Bladder small-diameter DRG neuron;
Channel(s): I Na,t; I Na, slow inactivation; I Na,p; I A, slow; I_KD; I K,Ca; I M; I_K,Na; I L high threshold; I N; I p,q; I R; I T low threshold; I h; I TRPM8; I Cl,Ca; Na/K pump; Na/Ca exchanger; Ca pump; IK Bkca; I Ca SOCC; IK Skca;
Gap Junctions:
Receptor(s):
Gene(s):
Transmitter(s):
Simulation Environment: NEURON;
Model Concept(s): Detailed Neuronal Models; Calcium dynamics; Action Potentials; Nociception;
Implementer(s): Mandge, Darshan [darshanmandge at iitb.ac.in];
Search NeuronDB for information about:  I Na,p; I Na,t; I L high threshold; I N; I T low threshold; I p,q; I M; I h; I Cl,Ca; I K,Ca; I A, slow; Na/Ca exchanger; I R; I_K,Na; Na/K pump; I_KD; Ca pump; I TRPM8; I Na, slow inactivation; IK Bkca; I Ca SOCC; IK Skca;
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