Difference between revisions of "Support:Documents:Examples:Estimate Change of Neurotransmitter"

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[[Image:Model.jpg]]
 
[[Image:Model.jpg]]
 
Generally, there are two separate injections of tracer for ntPET: one for the rest condition (without any stimuli) and the other for the activation conditon (after a stimulus). C<sub>p</sub> is the pasma concentration of tracer at the first injection (the "rest" condition), F and B are free (unbound) and bound molar concentrations of tracer after the first injection  C<sub>p2</sub> is the pasma concentration of tracer at the second injection (the "activation" condition), F2 and B2 are free (unbound) and bound molar concentrations of tracer after the second injection. F<sup>en</sup> and B<sup>en</sup> are free and bound molar concentrations of a neurotransmitter released by endogenous ligand after a stimulus.
 
  
 
This model can be described by the differential equations:
 
This model can be described by the differential equations:
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dB/dt = K<sub>on</sub>[B<sub>max</sub> - B -B2 - B<sup>en</sup>]F - k<sub>off</sub>B
 
dB/dt = K<sub>on</sub>[B<sub>max</sub> - B -B2 - B<sup>en</sup>]F - k<sub>off</sub>B
  
 +
Generally, there are two separate injections of tracer for ntPET: one for the rest condition (without any stimuli) and the other for the activation conditon (after a stimulus).
 +
C<sub>p</sub> is the pasma concentration of tracer at the first injection (the "rest" condition).
 +
F and B are free (unbound) and bound molar concentrations of tracer after the first injection 
 +
C<sub>p2</sub> is the pasma concentration of tracer at the second injection (the "activation" condition).
 +
F2 and B2 are free (unbound) and bound molar concentrations of tracer after the second injection.
 +
F<sup>en</sup> and B<sup>en</sup> are free and bound molar concentrations of a neurotransmitter released by endogenous ligand after a stimulus.
  
  

Revision as of 20:17, 25 February 2009

Model of Neurotransmitter PET (ntPET)

Overview

The changes of endogenous neurotransmitter by PET scanning after a stimulus has been proved with different approaches. In stead of detecting the increase or decrease of a neurotransmitter, it is important to characterize the temporal change of a neurotransmitter after a stimulus. Morris proposed the new technique (called ntPET) for capturing the dynamic changes of a neurotransmitter after a stimulus and demonstrated the ability of this method to reconstruct the temporal characteistics of an enhance in neurotransmitter concentration.

Here we present a general model of ntPET, which can be simplified to Morris' model.

Model.jpg

This model can be described by the differential equations:

dF/dt = K1Cp - K2F - Kon[Bmax - B -B2 - Ben]F + koffB

dB/dt = Kon[Bmax - B -B2 - Ben]F - koffB

Generally, there are two separate injections of tracer for ntPET: one for the rest condition (without any stimuli) and the other for the activation conditon (after a stimulus). Cp is the pasma concentration of tracer at the first injection (the "rest" condition). F and B are free (unbound) and bound molar concentrations of tracer after the first injection Cp2 is the pasma concentration of tracer at the second injection (the "activation" condition). F2 and B2 are free (unbound) and bound molar concentrations of tracer after the second injection. Fen and Ben are free and bound molar concentrations of a neurotransmitter released by endogenous ligand after a stimulus.


Implementing the Compartment Model

Create a new model for ntPET