Warning: foreach() argument must be of type array|object, bool given in /var/www/html/web/app/themes/studypress-core-theme/template-parts/header/mobile-offcanvas.php on line 20

The respiratory symptoms of asthma result from constriction of the bronchi and bronchioles of the lungs, caused by contraction of the smooth muscle of their walls. Raising [cAMP] in the smooth muscle reverses the constriction of the bronchi and bronchioles. Explain the therapeutic effects of albuterol, an inhaled \(\beta\)-adrenergic agonist, in treating asthma. Would you expect this drug to have any side effects? If so, what design change could you make to the drug to minimize side effects?

Short Answer

Expert verified
Albuterol induces bronchodilation by increasing cAMP in bronchial smooth muscle, with possible side effects like increased heart rate. Modifying it to target lung-specific \\(\\beta_2\\) receptors can minimize side effects.

Step by step solution

01

Understanding Albuterol's Mechanism

Albuterol functions as a \(\beta\)-adrenergic agonist. This means that it binds to and activates \(\beta\)-adrenergic receptors on the smooth muscle cells surrounding the bronchi and bronchioles. These receptors are part of the sympathetic nervous system, which when activated, leads to an increase in intracellular cyclic adenosine monophosphate (cAMP).
02

Increasing cAMP and Smooth Muscle Relaxation

The increase in cAMP in the smooth muscle of the bronchi and bronchioles results in muscle relaxation. Since the constriction of these muscles is a primary symptom of asthma, albuterol effectively leads to bronchodilation—widening of the airways—which alleviates the respiratory symptoms of asthma.
03

Considering Side Effects

Albuterol, by activating \(\beta\)-adrenergic receptors, isn't only specific to those in the lungs. These receptors are also present in the heart and other tissues. Thus, side effects can include increased heart rate (tachycardia), jitteriness, or tremors, because of stimulation of \(\beta\)-receptors in these areas.
04

Design Modifications to Minimize Side Effects

To minimize side effects, the drug can be modified to target \(\beta_2\)-adrenergic receptors specifically, rather than both \(\beta_1\) and \(\beta_2\) receptors. \(\beta_2\)-receptors are predominantly found in the lungs, whereas \(\beta_1\)-receptors are primarily found in the heart. Additionally, altering the drug formulation to limit systemic absorption and designing delivery systems that target the lung more directly can reduce side effects.

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with Vaia!

Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Bronchodilation
Asthma is a respiratory condition where the airways of the lungs (the bronchi and bronchioles) become constricted. This can make breathing difficult and lead to symptoms such as wheezing and coughing. When discussing asthma treatment, a key goal is to achieve **bronchodilation**.

Bronchodilation refers to the widening of the airways, which helps increase airflow to the lungs. Treatment that leads to bronchodilation works by relaxing the smooth muscles that encircle the bronchi and bronchioles, allowing them to expand. This action directly alleviates the respiratory symptoms of asthma, making it easier to breathe. By understanding bronchodilation, we can better appreciate how medications like albuterol help in asthma management.
Beta-Adrenergic Agonist
Albuterol is classified as a **beta-adrenergic agonist**. This type of medication works by interacting with the beta-adrenergic receptors located on the surface of smooth muscle cells.

When albuterol is inhaled, it binds to these receptors, particularly targeting those in the airways. These receptors play a role in the sympathetic nervous system, which controls the "fight or flight" responses in the body. By activating these beta-adrenergic receptors, albuterol sets off a cascade of events inside the muscle cells.

This activation leads to increased levels of cyclic adenosine monophosphate (cAMP), which we'll explore more shortly. But, in essence, it is this increase that triggers muscle relaxation, leading to bronchodilation.
Drug Side Effects
While bronchodilators like albuterol are effective in treating asthma, they can also have **drug side effects**. This occurs because beta-adrenergic receptors are spread throughout various parts of the body, not just the lungs.

For instance, activating beta-adrenergic receptors in the heart can lead to increased heart rate (tachycardia), or cause symptoms like jitteriness and tremors. These side effects are generally due to albuterol's interaction with \(\beta_1\) and \(\beta_2\) adrenergic receptors.

To minimize these side effects, drug design modifications focus on improving the selectivity of albuterol for \(\beta_2\) receptors which are mainly in the lungs, rather than \(\beta_1\) receptors predominantly found in the heart.
Cyclic Adenosine Monophosphate (cAMP)
A crucial player in the relief of asthma symptoms is **cyclic adenosine monophosphate (cAMP)**. When the beta-adrenergic receptors are activated by albuterol, they increase the levels of cAMP within the smooth muscle cells.

The presence of cAMP is vital because it starts a chain reaction inside the cells that causes the muscles surrounding the bronchi and bronchioles to relax.

The relaxation of these muscles permits the widening of the airways, a process known as bronchodilation. This increase in cAMP is one of the key biological processes that help open up the airways during an asthma attack.
Pharmacology
In **pharmacology**, understanding how drugs work in the body is essential. With regards to asthma treatment, pharmacology helps us delve into the mechanisms of drugs like albuterol.

Standard pharmacological practice examines how drugs interact with their target receptors—like how albuterol acts on beta-adrenergic receptors to promote bronchodilation. Furthermore, pharmacology explores how a drug's formulation and delivery can be optimized to maximize its therapeutic effects while minimizing adverse effects.

By using pharmacological principles, scientists can continue to refine asthma treatments, helping individuals breathe more easily and lead healthier lives.

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

The sensations of heat and cold are transduced by a group of temperature-gated cation channels. For example, TRPV1, TRPV3, and TRPM8 are usually closed, but they open at different temperatures. TRPV1 opens at \(\geq 43{ }^{\circ} \mathrm{C}\), TRPV 3 opens at \(\geq 33{ }^{\circ} \mathrm{C}\), and TRPM8 opens at \(<25^{\circ} \mathrm{C}\). These channel proteins are expressed in sensory neurons known to be responsible for temperature sensation. a. Propose a reasonable model to explain how exposing a sensory neuron containing TRPV1 to high temperature leads to a sensation of heat. b. Capsaicin, one of the active ingredients in "hot" peppers, is an agonist of TRPV1. Capsaicin shows \(50 \%\) activation of the TRPV1 response at a concentration of \(32 \mathrm{~nm}-\) a property known as \(\mathrm{EC}_{50}\). Explain why even a very few drops of hot pepper sauce can taste very "hot" without actually burning you. c. Menthol, one of the active ingredients in mint, is an agonist of TRPM8 \(\left(\mathrm{EC}_{50}=30 \mu \mathrm{M}\right)\) and TRPV3 \(\left(\mathrm{EC}_{50}=20 \mathrm{mM}\right)\). What sensation would you expect from contact with low levels of menthol? With high levels?

In principle, the physiological effects of epinephrine should be mimicked by addition of cAMP to the target cells. In practice, addition of cAMP to intact target cells elicits only a minimal physiological response. Why? When the structurally related derivative dibutyryl cAMP (shown) is added to intact cells, the expected physiological response is readily apparent. Explain the basis for the difference in cellular response to these two substances. Dibutyryl cAMP is widely used in studies of cAMP function.

Explain why some children with retinoblastoma develop multiple tumors of the retina in both eyes, whereas others have a single tumor in only one eye.

Explain why mutations in tumor suppressor genes are recessive (both copies of the gene must be defective for the regulation of cell division to be defective), whereas mutations in oncogenes are dominant.

For each of the situations listed, provide a plausible explanation for how it could lead to unrestricted cell division. a. Colon cancer cells often contain mutations in the gene encoding the prostaglandin \(\mathrm{E}_{2}\) receptor. \(\mathrm{PGE}_{2}\) is a growth factor required for the division of cells in the gastrointestinal tract. b. Kaposi sarcoma, a common tumor in people with untreated AIDS, is caused by a virus carrying a gene for a protein similar to the chemokine receptors CXCR1 and CXCR2. Chemokines are cell-specific growth factors. c. Adenovirus, a tumor virus, carries a gene for the protein E1A, which binds to the retinoblastoma protein, pRb. (Hint: See Fig, 12-40.) d. An important feature of many oncogenes and tumor suppressor genes is their cell-type specificity. For example, mutations in the \(\mathrm{PGE}_{2}\) receptor are not typically found in lung tumors. Explain this observation. (Note that \(\mathrm{PGE}_{2}\) acts through a GPCR in the plasma membrane.)

See all solutions

Recommended explanations on Chemistry Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.

Sign-up for free