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Related Concept Videos

Pharmacodynamic Models: Direct Effect Model and Indirect Response Model01:29

Pharmacodynamic Models: Direct Effect Model and Indirect Response Model

Pharmacodynamic models are essential tools in understanding the relationship between drug concentrations and their effects on biological systems. By characterizing the dynamics of drug action, these models guide dose selection, optimize therapeutic efficacy, and inform the development of new drugs. Two major classes of pharmacodynamic models include direct effect and indirect response models.Direct Effect ModelsDirect effect models describe the immediate relationship between drug concentration...
Pharmacodynamic Models: Additive and Proportional Drug Effect Model01:09

Pharmacodynamic Models: Additive and Proportional Drug Effect Model

Drug response models describe how pharmacological agents interact with biological systems to produce measurable effects. Baseline responses are inherent physiological activities without a drug significantly influencing the observed pharmacological outcomes. Depending on the drug response model employed, these baseline responses may combine with the drug's effect in either an additive or proportional manner.Additive Drug Response ModelIn the additive model, the drug effect is independent of the...
Pharmacodynamic Models: Emax Drug–Concentration Effect Model01:18

Pharmacodynamic Models: Emax Drug–Concentration Effect Model

The Emax drug-concentration effect model is central to pharmacodynamics in drug discovery and development. This model is predicated on the receptor occupancy theory, which posits that the effect of a drug is directly related to the number of receptors occupied by the drug and the resultant complex formation.The model describes the reversible interaction between a drug (C) and a receptor (R) to form a drug-receptor complex (RC). The kinetics of this interaction are quantified by an equation that...
Pharmacodynamic Models: Link Model and Systems Pharmacodynamic Model01:14

Pharmacodynamic Models: Link Model and Systems Pharmacodynamic Model

The link model is a fundamental pharmacokinetic-pharmacodynamic (PK–PD) approach to account for delayed drug responses when the observed effect does not immediately correlate with the drug's plasma concentration peak. This delay is mathematically addressed by introducing an effect compartment concentration, Ce, which is kinetically linked to the plasma concentration, Cp, via a first-order rate constant, ke0. The linkage allows for a more accurate prediction of drug effects over time. A higher...
Pharmacodynamic Models: Overview01:27

Pharmacodynamic Models: Overview

Pharmacodynamic (PD) responses describe the interaction between a drug and its biological target, culminating in a physiological effect. These responses can be classified into different types: continuous variables, such as blood glucose levels; categorical outcomes, like survival rates; and time-to-event metrics, such as disease progression. Understanding and modeling PD responses are critical for optimizing drug efficacy and safety.PD models describe the relationship between drug concentration...
Induced-fit Model01:13

Induced-fit Model

Most chemical reactions in cells require enzymes—biological catalysts that speed up the reaction without being consumed or permanently changed. They reduce the activation energy needed to convert the reactants into products. Enzymes are proteins, that usually work by binding to a substrate—a reactant molecule that they act upon.
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Modeling Fast-scan Cyclic Voltammetry Data from Electrically Stimulated Dopamine Neurotransmission Data Using QNsim1.0
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A dynamic causal model for evoked and induced responses.

Chun-Chuan Chen1, Stefan J Kiebel, James M Kilner

  • 1Wellcome Trust Centre for Neuroimaging, Sobell Department of Motor Neuroscience and Movement Disorders, Institute of Neurology, University College London, UK. cchen@ncu.edu.tw

Neuroimage
|August 13, 2011
PubMed
Summary

This study introduces a new model to analyze brain

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Area of Science:

  • Neuroscience
  • Computational Neuroscience
  • Brain Imaging

Background:

  • Neuronal responses comprise evoked and induced components, potentially reflecting distinct processes.
  • Induced responses are often linked to top-down modulation, contrasting with bottom-up evoked responses.
  • Current methods assume linear decomposition, which may fail for nonlinear neuronal processes.

Purpose of the Study:

  • To develop a novel Dynamic Causal Model (DCM) capable of simultaneously modeling evoked and induced neuronal responses.
  • To investigate the underlying mechanisms, specifically coupling and changes in coupling, that generate induced responses.
  • To empirically test the model's validity and explore the role of backward connections in motor control circuits.

Main Methods:

  • Proposed a Dynamic Causal Model (DCM) for simultaneous analysis of evoked and induced neuronal responses.
  • Utilized Bayesian Model Selection to validate the model with synthetic data.
  • Applied the DCM to magnetoencephalography (MEG) data from a hand grip task.

Main Results:

  • The proposed DCM successfully distinguished between models with and without induced components in synthetic data.
  • Analysis of MEG data provided evidence that induced responses are associated with backward message passing.
  • Demonstrated that evoked and induced components share underlying mechanisms and coupling characteristics.

Conclusions:

  • The novel DCM offers a robust framework for simultaneously modeling evoked and induced neuronal responses.
  • Findings suggest induced responses in motor control circuits are primarily mediated by backward connections.
  • The study highlights shared mechanisms between evoked and induced components, advancing our understanding of neural dynamics.