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Controlling KCa channels with different Ca2+ buffering models in Purkinje cell (Anwar et al. 2010)
Accession: 138382
In this work, we compare the dynamics of different buffering models during generation of a dendritic Ca2+ spike in a single compartment model of a Purkinje cell dendrite. The Ca2+ buffering models used are 1) a single Ca2+ pool, 2) two Ca2+ pools respectively for the fast and slow transients, 3) a detailed calcium model with buffers, pump (Schmidt et al., 2003), and diffusion and 4) a calcium model with buffers, pump and diffusion compensation. The parameters of single pool and double pool are tuned, using Neurofitter (Van Geit et al., 2007), to approximate the behavior of detailed calcium dynamics over range of 0.5 µM to 8 µM of intracellular calcium. The diffusion compensation is modeled using a buffer-like mechanism called DCM. To use DCM robustly for different diameter compartments, its parameters are estimated, using Neurofitter (Van Geit et al., 2007), as a function of compartment diameter (0.8 µm-20 µm).
Reference: Anwar H, Hong S, De Schutter E (2010) Controlling Ca(2+)-Activated K (+) Channels with Models of Ca (2+) Buffering in Purkinje Cells. Cerebellum [PubMed]
Citations  Citation Browser
Model Information (Click on a link to find other models with that property)
Model Type:  Dendrite;
Brain Region(s)/Organism:  
Cell Type(s):  Cerebellar purkinje cell;  
Channel(s):  I K,Ca; I Calcium;  
Gap Junctions:  
Receptor(s):  
Gene(s):  
Transmitter(s):  
Simulation Environment:  Neuron;
Model Concept(s):  Calcium dynamics;
Implementer(s):  
Search NeuronDB for information about:  Cerebellar purkinje cell; I K,Ca; I Calcium;
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AnwarEtAl2010
ReadMe.htm
ReadMe.rtf
CALC.mod
CALC_ca2_DP.mod
CALC_DP.mod
CaT3_1.mod
CaT3_1_DP.mod
cdp3.mod
cdp5.mod
leak.mod
mslo.mod
mslo_DP.mod
newCaP.mod
newCaP_DP.mod
SK2.mod
SK2_DP.mod
morphology_mechanisms_CaSpikes_DCM.hoc
morphology_mechanisms_CaSpikes_DM.hoc
morphology_mechanisms_CaSpikes_DP.hoc
morphology_mechanisms_CaSpikes_SP.hoc
morphology_mechanisms_CaTransients.hoc
morphology_mechanisms_DM.hoc
mosinit.hoc
CaBufferingModels.hoc
runCaSpikesDCM.hoc
runCaSpikesDM.hoc
runCaSpikesDP.hoc
runCaSpikesSP.hoc
runCaTransients.hoc
runDM.hoc
CaTransientsDisplay.ses
CaSpikesDisplay_DM.ses
BuffersNPumps.ses
CaSpikesDisplay_DCM.ses
CaSpikesDisplay_DP.ses
CaSpikesDisplay_SP.ses
CaSpikeProtocol.dat
                            
Calcium buffering models explanatory note:

Model Published in:

Anwar H, Hong S, De Schutter E (2010) Controlling Ca2+-activated K+
channels with models of Ca2+ buffering in Purkinje cell. Cerebellum *

* Available as Open Access

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/20981513

Email contact: anwar@oist.jp

Model description:

In this work, we compare the dynamics of different buffering models
during generation of a dendritic Ca2+ spike in a single compartment
model of a Purkinje cell dendrite.  The Ca2+ buffering models used are
1) a single Ca2+ pool, 2) two Ca2+ pools respectively for the fast and
slow transients, 3) a detailed calcium model with buffers, pump
(Schmidt et al., 2003), and diffusion and 4) a calcium model with
buffers, pump and diffusion compensation. The parameters of single
pool and double pool are tuned, using Neurofitter (Van Geit et al.,
2007), to approximate the behavior of detailed calcium dynamics over
range of 0.5 µM to 8 µM of intracellular calcium. The diffusion
compensation is modeled using a buffer-like mechanism called DCM. To
use DCM robustly for different diameter compartments, its parameters
are estimated, using Neurofitter (Van Geit et al., 2007), as a
function of compartment diameter (0.8 µm-20 µm).

Scripts Explanation:

Go to the folder containing the model scripts. Run nrnivmodl. Then
type nrngui CaBufferingModels.hoc

A panel with six buttons will appear on the screen.

1.  Detailed Calcium dynamics model: Click on this button to see the
behavior of detailed calcium dynamics model. It will display nine
plots arranged in three rows and three columns. The plot on the top
left corner shows calcium transients with peak amplitude of 0.5 µM, 1
µM and 2 µM. These transients were generated using a voltage step
command (as shown in Figure 1a in Anwar et al., 2010) with different
maximal conductance values of P-type Ca2+ channel. All the other plots
show corresponding behavior of buffers and pump current. These plots
are same as Figure 2 in Anwar et al., 2010.

2.  Calcium transients using different buffering models: Click on this
button to see the calcium transients with peak amplitude of 2 µM,
generated using single pool, double pool, detailed calcium dynamics
model and DCM. The parameters of single pool, double pool and DCM were
fitted using Neurofitter (Van Geit et al., 2007) as described in Anwar
et al., 2010. This plot is similar to Figure 3c and Figure 6 in Anwar
et al., 2010 except that the Ca2+ transient in these scripts are shown
for diameter 4 µm.

3.  Calcium spikes using single pool model: Click on this button to
see the calcium spikes generated using single pool model. The maximal
conductance values for P-type and T-type Ca2+ channels and BK-type and
SK-type Ca2+ activated K+ channels were tuned using Neurofitter (Van
Geit et al., 2007) and are presented in Anwar et al., 2010. Note that
the parameter values used for single pool in this plot are different
than those used in plot showing calcium transients. The parameter
values of single pool used to generate calcium spikes in this plot are
obtained using experimental trace (shown in Figure 1b in Anwar et al.,
2010) as a voltage command. This plot exists in Figure 7d in Anwar et
al., 2010.

4.  Calcium spikes using double pool model: Click on this button to
see the calcium spikes generated using double pool model. The maximal
conductance values for P-type and T-type Ca2+ channels and BK-type and
SK-type Ca2+ activated K+ channels were tuned using Neurofitter (Van
Geit et al., 2007) and are presented in Anwar et al., 2010. Note that
the parameter values used for double pool in this plot are different
than those used in plot showing calcium transients. The parameter
values of double pool used to generate calcium spikes in this plot are
obtained using experimental trace (shown in Figure 1b in Anwar et al.,
2010) as a voltage command. This plot exists in Figure 7d in Anwar et
al., 2010.

5.  Calcium spikes using detailed model: Click on this button to see
the calcium spikes generated using detailed model. The maximal
conductance values for P-type and T-type Ca2+ channels and BK-type and
SK-type Ca2+ activated K+ channels were tuned using Neurofitter (Van
Geit et al., 2007) and are presented in Anwar et al., 2010. This plot
exists in Figure 7c in Anwar et al., 2010.

6.  Calcium spikes using DCM: Click on this button to see the calcium
spikes generated using DCM. The maximal conductance values for P-type
and T-type Ca2+ channels and BK-type and SK-type Ca2+ activated K+
channels were tuned using Neurofitter (Van Geit et al., 2007) and are
presented in Anwar et al., 2010. This plot exists in Figure 7c in
Anwar et al., 2010.

References

Anwar H, Hong S, De Schutter E (2010) Controlling Ca2+-activated K+
channels with models of Ca2+ buffering in Purkinje cell. Cerebellum,
in print.

van Geit W, Achard P, de Schutter E (2007) Neurofitter: a parameter
tuning package for a wide range of electrophysiological neuron
models. Front Neuroinform 1:1

Schmidt H, Stiefel K, Racay P, Schwaller B, Eilers J (2003) Mutational
analysis of dendritic Ca2+ kinetics in rodent Purkinje cells: role of
parvalbumin and calbindin D28k. J Physiol 551:13-32


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