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Related Concept Videos

Drug-Receptor Interactions01:29

Drug-Receptor Interactions

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.
Drug-Receptor Interaction: Antagonist01:28

Drug-Receptor Interaction: Antagonist

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...
Drug toxicity: Drug–Drug Interaction01:30

Drug toxicity: Drug–Drug Interaction

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...
Quantitative Aspects of Drug-Receptor Interaction01:30

Quantitative Aspects of Drug-Receptor Interaction

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 Kd...
Combined Effects of Drugs: Synergism01:27

Combined Effects of Drugs: Synergism

Synergism is a useful mechanism where combining two or more drugs is more effective than each constituent used alone. Such combinations are also called supra-additive interactions. The drugs collectively enhance the final therapeutic effect by acting on different targets. Another advantage is that the low dose of each constituent drug is sufficient to achieve the desired effect. This helps reduce the duration of therapy and lower the adverse effects of these drugs.
Such synergistic combinations...
Drug-Receptor Interaction: Agonist01:25

Drug-Receptor Interaction: Agonist

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 ligand's action.

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A Data Integration Workflow to Identify Drug Combinations Targeting Synthetic Lethal Interactions
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Using a shallow linguistic kernel for drug-drug interaction extraction.

Isabel Segura-Bedmar1, Paloma Martínez, Cesar de Pablo-Sánchez

  • 1Computer Science Department, Carlos III University of Madrid, Leganés, Spain. isegura@inf.uc3m.es

Journal of Biomedical Informatics
|May 7, 2011
PubMed
Summary

This study introduces a machine learning approach for extracting drug-drug interactions (DDIs) from biomedical texts. The proposed shallow linguistic kernel method outperforms previous approaches and introduces the first DDI corpus for research.

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Area of Science:

  • Biomedical Informatics
  • Natural Language Processing
  • Pharmacology

Background:

  • Drug-drug interactions (DDIs) are critical in healthcare, necessitating efficient literature review methods.
  • Current information extraction (IE) techniques lack a dedicated approach for DDI extraction from biomedical texts.

Purpose of the Study:

  • To evaluate a machine learning-based method for automated DDI extraction.
  • To compare the performance of a shallow linguistic kernel against a pattern-based approach for DDI identification.
  • To introduce the first benchmark corpus for DDI extraction research.

Main Methods:

  • Developed a supervised machine learning model using a shallow linguistic kernel.
  • Created and annotated the DrugDDI corpus, containing 3169 DDIs.
  • Conducted experiments to optimize the shallow linguistic kernel's configuration parameters.

Main Results:

  • The shallow linguistic kernel achieved a precision of 51.03%, recall of 72.82%, and F-measure of 60.01% on the DrugDDI corpus.
  • The machine learning approach demonstrated superior performance compared to the previously proposed pattern-based method.
  • The DrugDDI corpus provides a valuable resource for future DDI extraction research.

Conclusions:

  • The shallow linguistic kernel is an effective method for automated DDI extraction from biomedical literature.
  • This study presents the first comprehensive solution for DDI extraction, supported by a novel annotated corpus.
  • The developed corpus is expected to foster further advancements in DDI extraction methodologies.