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A biophysically detailed computational model of urinary bladder small DRG neuron soma

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 Ca(2+)-activated K(+) (SK(Ca)) channels which were earlier thought to be gated solely by...

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Detalles Bibliográficos
Autores principales: Mandge, Darshan, Manchanda, Rohit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6066259/
https://www.ncbi.nlm.nih.gov/pubmed/30020934
http://dx.doi.org/10.1371/journal.pcbi.1006293
Descripción
Sumario: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 Ca(2+)-activated K(+) (SK(Ca)) channels which were earlier thought to be gated solely by intracellular Ca(2+) concentration ([Ca](i)) have recently been shown to exhibit inward rectification with respect to membrane potential. The effect of SK(Ca) inward rectification on the excitability of these neurons is unknown. Furthermore, studies on the role of K(Ca) 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 neuron soma constrained by physiological data. The model includes twenty-two major known membrane mechanisms along with intracellular Ca(2+) dynamics comprising Ca(2+) diffusion, cytoplasmic buffering, and endoplasmic reticulum (ER) and mitochondrial mechanisms. Using modelling studies, we show that inward rectification of SK(Ca) is an important parameter regulating neuronal repetitive firing and that its absence reduces action potential (AP) firing frequency. We also show that SK(Ca) is more potent in reducing AP spiking than the large-conductance K(Ca) channel (BK(Ca)) in these neurons. Moreover, BK(Ca) was found to contribute to the fast AHP (fAHP) and SK(Ca) to the medium-duration (mAHP) and slow AHP (sAHP). We also report that the slow inactivating A-type K(+) channel (slow K(A)) 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.