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Related Concept Videos

Antiasthma Drugs: β2-Adrenoceptor Agonists01:25

Antiasthma Drugs: β2-Adrenoceptor Agonists

Bronchodilators are critical in managing asthma, a chronic respiratory condition characterized by airway constriction due to inflammation and hyper-reactivity. Specifically, bronchodilators ease this constriction by relaxing the bronchial muscles, facilitating easier breathing.
One class of bronchodilators includes β2-adrenoceptor agonists. These agents target the β2-adrenoceptors located on bronchial smooth muscle cells. By stimulating these receptors, β2-agonists induce relaxation in these...
Antihypertensive Drugs: Types of β-Blockers01:28

Antihypertensive Drugs: Types of β-Blockers

β receptors are classified into three subclasses: β1, β2, and β3. β1 receptors are primarily located in the heart and kidneys. When they get activated, they increase heart rate, contractility, and renin release. This process enhances blood pressure and aids in stress management. In contrast, β2 receptors are situated mainly in the lungs, blood vessels, and skeletal muscles. Upon activation, they trigger smooth muscle relaxation, causing bronchodilation and vasodilation. This widens airways and...
Asthma-II: Pathophysiology and Classification01:26

Asthma-II: Pathophysiology and Classification

Asthma is a prevalent chronic respiratory condition marked by inflammation and hyperresponsiveness of the airways. Its pathophysiology involves complex interactions among inflammatory pathways, immune responses, and neural mechanisms.
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Pharmacogenetics of Drug Targets: β₂-Adrenergic Receptors, Apo E, Thymidylate Synthase01:11

Pharmacogenetics of Drug Targets: β₂-Adrenergic Receptors, Apo E, Thymidylate Synthase

Genetic polymorphisms in drug targets have emerged as critical determinants of interindividual variability in drug response and toxicity. Pharmacogenomic investigations increasingly focus on identifying these variations to personalize and optimize therapeutic interventions. A drug target may be a receptor, enzyme, or signaling protein involved in pharmacologic responses or disease-related pathways. While early pharmacogenetic studies focused primarily on drug metabolism, current research...
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Asthma-IV: Diagnostic and Management

The diagnosis and management of asthma are comprehensive, encompassing clinical assessments, lung function tests, and pharmacological interventions. Here's an overview:
Clinical Assessment for Asthma:
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Asthma III: Clinical Manifestations01:13

Asthma III: Clinical Manifestations

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Related Experiment Video

Updated: Jul 5, 2026

Bronchial Thermoplasty: A Novel Therapeutic Approach to Severe Asthma
14:39

Bronchial Thermoplasty: A Novel Therapeutic Approach to Severe Asthma

Published on: November 4, 2010

Confirmed beta16 Arg/Arg polymorphism in a patient with uncontrolled asthma.

Nicole L Metzger1, Denise R Kockler, Leigh Anne Hylton Gravatt

  • 1Virginia Commonwealth University Health System, Medical College of Virginia Hospitals, Richmond, VA 23298, USA.

The Annals of Pharmacotherapy
|April 24, 2008
PubMed
Summary

Patients with the beta(16) Arg/Arg polymorphism may experience uncontrolled asthma with short-acting beta(2)-agonists. Genotyping and considering anticholinergics may improve asthma outcomes in these individuals.

Related Experiment Videos

Last Updated: Jul 5, 2026

Bronchial Thermoplasty: A Novel Therapeutic Approach to Severe Asthma
14:39

Bronchial Thermoplasty: A Novel Therapeutic Approach to Severe Asthma

Published on: November 4, 2010

Area of Science:

  • Pharmacogenomics
  • Respiratory Medicine
  • Clinical Genetics

Background:

  • Uncontrolled asthma necessitates exploring genetic factors influencing treatment response.
  • The beta(16) Arg/Arg polymorphism is prevalent in certain populations and may impact beta-agonist efficacy.

Observation:

  • A patient with uncontrolled asthma and frequent short-acting beta(2)-agonist (SABA) use was found to have the beta(16) Arg/Arg genotype.
  • Despite adherence to asthma medications, the patient experienced multiple exacerbations requiring hospitalization and intubation.

Findings:

  • The beta(16) Arg/Arg genotype is associated with a potential decrease in sensitivity or increased desensitization to beta(2)-agonists.
  • Clinical outcomes, including asthma symptoms and exacerbations, may worsen with regular SABA use in individuals with this polymorphism.

Implications:

  • Beta(2)-adrenoreceptor genotyping can identify patients at risk for poor outcomes with standard asthma therapies.
  • Anticholinergic medications may offer a beneficial alternative to beta(2)-agonists as a primary rescue therapy for patients with the Arg/Arg polymorphism.