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

Drug toxicity: Drug–Drug Interaction01:30

Drug toxicity: Drug–Drug Interaction

421
Drug–drug interactions can precipitate toxicity through multiple mechanisms. Absorption interactions alter how drugs enter the body, exemplified when ranitidine increases the absorption of basic drugs, while cholestyramine decreases the levels of propranolol. Protein binding interactions occur when drugs share the same binding sites on plasma proteins. Drugs like aspirin and warfarin, when bound in excess, can lead to increased free drug concentrations, enhancing the potential for...
421
Pharmacokinetics: Drug–Drug Interactions01:25

Pharmacokinetics: Drug–Drug Interactions

804
Drug interactions occur when the pharmacological effect of one drug is altered by another substance, either enhancing or diminishing its activity. The drug whose activity is altered is known as the object drug, and the substance causing the alteration is called the agent drug or the precipitant. The net effects of these interactions are mostly undesirable, leading to decreased effectiveness or increased adverse effects. In rare cases, interactions can be beneficial, such as the enhanced...
804
Drug-Receptor Interactions01:29

Drug-Receptor Interactions

8.2K
Drug-receptor interaction describes the binding of receptors by drugs, but not all drug-receptor interactions result in activation and tissue response. For instance, the binding of agonists activates the receptor to generate a cellular reaction, while antagonists bind to receptors without causing their activation.
Several parameters, such as the drug's affinity for its receptor and its efficacy, which is its ability to activate the receptor, determine the drug's effect on the tissue....
8.2K
Drug-Receptor Interaction: Antagonist01:28

Drug-Receptor Interaction: Antagonist

4.9K
An antagonist is a drug that binds strongly to a receptor without activating it. An antagonist prevents other molecules, such as neurotransmitters or hormones, from binding to the receptor and triggering a cellular response. Such interaction effectively hinders the normal physiological processes mediated by the receptor, resulting in various pharmacological effects depending on the specific receptor targeted.
Antagonists can be classified as competitive or noncompetitive based on their...
4.9K
Drug-Receptor Interaction: Agonist01:25

Drug-Receptor Interaction: Agonist

4.3K
Agonists are drugs that interact with specific receptors in the body to produce a biological response. When an agonist binds to a receptor, it activates or enhances the receptor's function, leading to physiological effects. The interaction between agonist drugs and receptors is crucial for their therapeutic action in various medical treatments.
Agonists can bind to receptors in different ways. Some agonists bind directly to the receptor's active site, mimicking the endogenous...
4.3K
Quantitative Aspects of Drug-Receptor Interaction01:30

Quantitative Aspects of Drug-Receptor Interaction

2.1K
The receptor occupancy theory connects a drug's response to the number of occupied receptors. With higher drug concentrations, more receptors are occupied, leading to increased responses. The formation of drug-receptor complexes involves association and dissociation rates, which reach equilibrium when the forward and backward reactions are equal. The equilibrium association constant (Ka) and its inverse, the equilibrium dissociation constant (Kd), indicate drug affinity. Higher Ka and lower...
2.1K

You might also read

Related Articles

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

Sort by
Same author

Tract-based χ-separation imaging differentiates multiple sclerosis from neuromyelitis optica spectrum disorder by mapping iron and myelin signatures.

BMC medical imaging·2026
Same author

A Bibliometric Analysis of Global Research Hotspots and Progress on Microbial Extracellular Polymeric Substances in Bioremediation.

Microorganisms·2026
Same author

Engineered bone-targeting <i>Lycium barbarum L.</i>-derived extracellular vesicle-like nanoparticles deliver miR167a-5p to regulate mitochondrial dynamics and metabolic reprogramming in alleviating osteoporosis.

Materials today. Bio·2026
Same author

Computed Tomography-Based Morphometric Analysis Reveals Intercondylar Notch Stenosis and Osteophytes Are Associated With Anterior Cruciate Ligament Injury.

Arthroscopy : the journal of arthroscopic & related surgery : official publication of the Arthroscopy Association of North America and the International Arthroscopy Association·2026
Same author

Perioperative serplulimab with neoadjuvant chemotherapy versus perioperative chemotherapy in PD-L1-positive gastric cancer (ASTRUM-006): a randomised, double-blind, multicentre, phase 3 study.

Lancet (London, England)·2026
Same author

Benchmarking Image-Based Motion-Correction Methods for Ultrasound Localization Microscopy.

Ultrasound in medicine & biology·2026
Same journal

A Knowledge-Guided Large Language Model Framework for Microbiome-Based Disease Diagnosis.

Proceedings. IEEE International Conference on Bioinformatics and Biomedicine·2026
Same journal

Vital Measurements of Hospitalized COVID-19 Patients as a Predictor of Long COVID: An EHR-based Cohort Study from the RECOVER Program in N3C.

Proceedings. IEEE International Conference on Bioinformatics and Biomedicine·2026
Same journal

Geospatial Analysis of Socioeconomic Equity and Environmental Factors Influencing Lung Cancer Prevalence in US.

Proceedings. IEEE International Conference on Bioinformatics and Biomedicine·2026
Same journal

Modeling TCR-pMHC Binding with Dual Encoders and Cross-Attention Fusion.

Proceedings. IEEE International Conference on Bioinformatics and Biomedicine·2026
Same journal

Utilizing Large Language Models for Zero-Shot Medical Ontology Extension from Clinical Notes.

Proceedings. IEEE International Conference on Bioinformatics and Biomedicine·2026
Same journal

Uncovering the Role of Neuropsychiatric Symptoms in Cognitive Impairment Progression.

Proceedings. IEEE International Conference on Bioinformatics and Biomedicine·2026
See all related articles

Related Experiment Video

Updated: Apr 25, 2026

A Data Integration Workflow to Identify Drug Combinations Targeting Synthetic Lethal Interactions
07:40

A Data Integration Workflow to Identify Drug Combinations Targeting Synthetic Lethal Interactions

Published on: May 27, 2021

3.4K

Text Mining Driven Drug-Drug Interaction Detection.

Su Yan1, Xiaoqian Jiang2, Ying Chen1

  • 1IBM Almaden Research Lab, San Jose, CA, USA.

Proceedings. IEEE International Conference on Bioinformatics and Biomedicine
|August 19, 2014
PubMed
Summary
This summary is machine-generated.

This study introduces a new computational method to predict drug-drug interactions by combining structured data with text mining. The novel approach significantly improves prediction accuracy, enhancing drug safety.

More Related Videos

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

21.0K
High-throughput Identification of Synergistic Drug Combinations by the Overlap2 Method
07:51

High-throughput Identification of Synergistic Drug Combinations by the Overlap2 Method

Published on: May 21, 2018

11.5K

Related Experiment Videos

Last Updated: Apr 25, 2026

A Data Integration Workflow to Identify Drug Combinations Targeting Synthetic Lethal Interactions
07:40

A Data Integration Workflow to Identify Drug Combinations Targeting Synthetic Lethal Interactions

Published on: May 27, 2021

3.4K
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

21.0K
High-throughput Identification of Synergistic Drug Combinations by the Overlap2 Method
07:51

High-throughput Identification of Synergistic Drug Combinations by the Overlap2 Method

Published on: May 21, 2018

11.5K

Area of Science:

  • Computational Biology
  • Bioinformatics
  • Drug Discovery

Background:

  • Drug-drug interactions (DDIs) pose a significant challenge in healthcare.
  • Predictive modeling for DDIs is hindered by the limited availability of structured data versus abundant, yet noisy, textual information.
  • Integrating heterogeneous data sources (structured and unstructured) is crucial for effective DDI prediction.

Purpose of the Study:

  • To develop a novel computational approach for predicting drug-drug interactions.
  • To enhance DDI prediction by effectively combining structured data with augmented text-mining features.
  • To improve the performance of predictive models in terms of discrimination and calibration.

Main Methods:

  • Leveraging augmented text-mining features derived from textual data.
  • Developing a logistic regression model incorporating these synthesized features.
  • Comparing the performance of the novel model against a model using only structured features.

Main Results:

  • The proposed model significantly outperformed the baseline model using only structured features.
  • Achieved higher predictive performance with an AUC of 96% vs. 91%, Sensitivity of 90% vs. 82%, and Specificity of 88% vs. 81%.
  • Identified and discussed interpretable "latent topics" from text mining as an intermediate result.

Conclusions:

  • Augmented text-mining features enhance the prediction of drug-drug interactions.
  • The developed computational approach offers improved accuracy and reliability for DDI identification.
  • This method provides a valuable tool for computational biology and healthcare research to ensure drug safety.