Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Pharmacodynamic Models: Additive and Proportional Drug Effect Model01:09

Pharmacodynamic Models: Additive and Proportional Drug Effect Model

61
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...
61
Pharmacodynamic Models: Direct Effect Model and Indirect Response Model01:29

Pharmacodynamic Models: Direct Effect Model and Indirect Response Model

100
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...
100
Cooperative Allosteric Transitions01:58

Cooperative Allosteric Transitions

9.4K
Cooperative allosteric transitions can occur in multimeric proteins, where each subunit of the protein has its own ligand-binding site. When a ligand binds to any of these subunits, it triggers a conformational change that affects the binding sites in the other subunits; this can change the affinity of the other sites for their respective ligands. The ability of the protein to change the shape of its binding site is attributed to the presence of a mix of flexible and stable segments in the...
9.4K
The Two-State Receptor Model01:29

The Two-State Receptor Model

3.5K
The two-state receptor model explains a drug's interaction with receptors, such as G protein-coupled receptors and ligand-gated ion channels, to induce or inhibit a biological response. When no natural ligands are present, a receptor exists in an equilibrium of inactive (Ri) and active (Ra) conformations. The inactive form does not produce a response, while the active form generates a basal effect known as constitutive activity.
The binding affinity of a drug determines its interaction with...
3.5K
Pharmacodynamic Models: Link Model and Systems Pharmacodynamic Model01:14

Pharmacodynamic Models: Link Model and Systems Pharmacodynamic Model

81
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...
81
Pharmacodynamic Models: Linear Concentration–Effect Model01:15

Pharmacodynamic Models: Linear Concentration–Effect Model

56
The linear concentration–effect model, underpinned by the principle that pharmacological effect (E) is directly proportional to plasma drug concentration (C), emerges as a pivotal simplification of the Emax model for conditions where C is significantly less than EC50. This model portrays a linear trajectory of the concentration–effect relationship when drug levels are markedly below the EC50 threshold.Despite its inherent assumption of continuous effect augmentation with increasing...
56

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Visual System Inspired Algorithm for Enhanced Visibility in Coronary Angiograms (VIAEVCA).

Biomimetics (Basel, Switzerland)·2025
Same author

Nonlinear multiscale analysis of coronary atherosclerotic vulnerable plaque artery: fluid-structural modeling with micromechanics.

Biomechanics and modeling in mechanobiology·2021
Same author

A predictive multiscale model for simulating flow-induced platelet activation: Correlating in silico results with in vitro results.

Journal of biomechanics·2021
Same author

New Insights into Valve Hemodynamics.

Rambam Maimonides medical journal·2020
Same author

Editorial: Integrating Visual System Mechanisms, Computational Models and Algorithms/Technologies.

Frontiers in bioengineering and biotechnology·2020
Same author

A Compound Computational Model for Filling-In Processes Triggered by Edges: Watercolor Illusions.

Frontiers in neuroscience·2019
Same journal

Multi-module collaborative optimization-driven fast speckle correlation imaging in variable environments.

Journal of the Optical Society of America. A, Optics, image science, and vision·2026
Same journal

Secrecy performance analysis of NOMA-UWOC systems over a vertically stratified WGG oceanic turbulence channel.

Journal of the Optical Society of America. A, Optics, image science, and vision·2026
Same journal

Backscattering of plane waves in a composite system containing a rough surface and anisotropic scatterers.

Journal of the Optical Society of America. A, Optics, image science, and vision·2026
Same journal

Aspherical surface construction methods based on extended Jacobi polynomials.

Journal of the Optical Society of America. A, Optics, image science, and vision·2026
Same journal

OCT sidelobe suppression method based on dual-path phase sinusoidal modulation and minimum value fusion.

Journal of the Optical Society of America. A, Optics, image science, and vision·2026
Same journal

Optical design concepts using wavelength-selective diffractive optics to enable miniaturized multimodal endoscopic imaging across separated spectral ranges.

Journal of the Optical Society of America. A, Optics, image science, and vision·2026
See all related articles

Related Experiment Video

Updated: Mar 26, 2026

Diagonal Method to Measure Synergy Among Any Number of Drugs
12:08

Diagonal Method to Measure Synergy Among Any Number of Drugs

Published on: June 21, 2018

19.7K

Single additive mechanism predicts lateral interactions effects-computational model.

Hava Matichin, Shmuel Einav, Hedva Spitzer

    Journal of the Optical Society of America. A, Optics, Image Science, and Vision
    |February 3, 2016
    PubMed
    Summary
    This summary is machine-generated.

    This study proposes a new model for lateral interactions (LI), suggesting a single facilitatory mechanism explains both facilitation and inhibition. This challenges existing models and offers a simpler explanation for visual perception phenomena.

    More Related Videos

    3D Modeling of Dendritic Spines with Synaptic Plasticity
    07:13

    3D Modeling of Dendritic Spines with Synaptic Plasticity

    Published on: May 18, 2020

    7.5K
    Author Spotlight: Evaluation of Protein-Condensate Dynamics in Live Human Cells
    06:48

    Author Spotlight: Evaluation of Protein-Condensate Dynamics in Live Human Cells

    Published on: January 5, 2024

    5.8K

    Related Experiment Videos

    Last Updated: Mar 26, 2026

    Diagonal Method to Measure Synergy Among Any Number of Drugs
    12:08

    Diagonal Method to Measure Synergy Among Any Number of Drugs

    Published on: June 21, 2018

    19.7K
    3D Modeling of Dendritic Spines with Synaptic Plasticity
    07:13

    3D Modeling of Dendritic Spines with Synaptic Plasticity

    Published on: May 18, 2020

    7.5K
    Author Spotlight: Evaluation of Protein-Condensate Dynamics in Live Human Cells
    06:48

    Author Spotlight: Evaluation of Protein-Condensate Dynamics in Live Human Cells

    Published on: January 5, 2024

    5.8K

    Area of Science:

    • Visual perception
    • Psychophysics
    • Neuroscience

    Background:

    • The mechanism of lateral interactions (LI) in visual perception remains poorly understood.
    • Existing models often incorporate both inhibitory and facilitatory mechanisms to explain LI.
    • These models are based on the traditional interpretation of threshold elevation in psychophysical experiments.

    Purpose of the Study:

    • To propose a novel interpretation of threshold elevation in psychophysical experiments.
    • To present a model demonstrating that a single facilitatory additive mechanism can explain LI phenomena.
    • To challenge the necessity of an additional inhibitory mechanism in LI models.

    Main Methods:

    • Development of a new theoretical model for lateral interactions.
    • Experimental validation using psychophysical methods.
    • Comparison of model predictions with existing psychophysical and neurophysiological data.

    Main Results:

    • The proposed model successfully predicts both facilitatory and inhibitory aspects of the LI phenomenon using only a facilitatory mechanism.
    • The model accurately accounts for LI across diverse stimulus configurations and parameters.
    • The model aligns with both historical and contemporary findings in psychophysics and neurophysiology.

    Conclusions:

    • A single facilitatory additive mechanism can explain the full spectrum of the lateral interactions phenomenon.
    • The traditional assumption of a significant inhibitory mechanism may not be necessary.
    • Lateral interactions likely contribute to the visual system's ability to infer continuity in gratings and textures.