Question

In: Anatomy and Physiology

The condition pulmonary fibrosis is caused by the replacement of elastic fibers in the lung with...

The condition pulmonary fibrosis is caused by the replacement of elastic fibers in the lung with inelastic collagen
fibers, which decreases the lungs' distensibility (the ability to stretch outward). Would pulmonary fibrosis make
inspiration or expiration difficult? Explain.

Solutions

Expert Solution

ANSWER -

Breathing is the process of the exchange of oxygen and carbon dioxide between external environment and body by the process of inspiration and expiration which is called respiration and this a very important process by which our body survives;

RESPIRATORY system is involved in breathing process and majorly lungs plays a major role in this

Normally as our body's every cell needs oxygen for survival so we inhale oxygen from the environment and these oxygen via lungs expansion goes till alveoli and from there get absorbed into the blood and circulates in whole body and waste carbon dioxide comes into the lungs and thrown out of the body.

Now this was the normal physiology of the breathing ; if there is any problem in respiratory tract means any hurdle embolism thrombosis stenosis etc all effects the breathing.

pulmonary fibrosis is the condition of scaring in the lungs in which fibers are deposited in the lungs which are inelastic in nature which are inelastic collagen fibers and so they decreasing the:

  1. size of lungs
  2. capacity
  3. elasticity or expandibltiy

these things when seen in the lungs affects the breathing very much because it becomes the arrival of proper oxygen in lungs , they wont expand also properly to recieve oxygen and so the gaseous exchange and oxygen supply in blood becomes difficult. and due to this brain and heart are also majorly affected and various illness symptoms are seen.

NOW due to the pulmonary fibrosis the process of expiration becomes more difficult when compared between the two because normally the expiration is the exhalation of air outside the body for which the diaphragm use to relax thoracic cavity volume decreases and which increases the pressure the lungs and air goes out but now in the case of pulmonary fibrosis the expand capacity of cavity is lost the lungs cannot relax well and as a result air got trapped in the lungs making the expiration very difficult.

SO comparatively the expiration process becomes more tough than inspiration which whole respiration tough.

Due to the loss of elastic capacity the relaxation of pleural cavity becomes tough and so the expiration also.


Related Solutions

A/. A lung with pulmonary fibrosis would exhibit which of the following characteristics? a. Decreased airway...
A/. A lung with pulmonary fibrosis would exhibit which of the following characteristics? a. Decreased airway resistance b. Decreased lung compliance c. Decreased PVR d. Decreased surface tension B. Which of the following indicate a patient is severe decrease in respiratory muscle inspiratory strength? a. MIP less than -50 cm H20 b. MIP less than -60 cm H20 c. MIP greater than -20 cm H20 d. MIP lower than -20 mm Hg C.  What is the term for alveolar ventilation without...
11. A pulmonary disorder that compromises the integrity of elastic protein fibers in the lungs may...
11. A pulmonary disorder that compromises the integrity of elastic protein fibers in the lungs may cause an increased compliance, poor elastic recoil and collapse of small bronchioles and alveoli. This patient would exhibit all of the following EXCEPT: A decrease in vital capacity A decrease in FEV1 An increase in % oxyhemoglobin saturation Chest pain due to air trapping 12. The majority of CO2 is transported in the blood as: Dissolved in plasma HCO3- Carbaminohemoglobin Carboxyhemoglobin 13 Patients with...
A pulmonary embolism is a blockage of the main arty of the lung or one of...
A pulmonary embolism is a blockage of the main arty of the lung or one of its branches by a clot from elsewhere in the body. The usual adult does of heparin given for pulmonary embolism is a one-time dose of 5000 units/IV followed by continuous IV infusion of 18 units/kg9f/hr. You have a stock solution of 10,000 units/10mL. A. How much of the stock solution would you need to administer initially (for the one-time does)? B. What IV flow...
What are the differences between elastic, collagen, and reticular fibers
What are the differences between elastic, collagen, and reticular fibers
A 68 year old woman with pulmonary fibrosis presents with worsening exertional dyspnea. 1) Describe pulmonary...
A 68 year old woman with pulmonary fibrosis presents with worsening exertional dyspnea. 1) Describe pulmonary fibrosis and include the changes to lung structure and function that are expected with this disease. 2) What changes to pulmonary function testing (capacities and volumes) would you expect to see in this type of patient? 3) What are the treatments for pulmonary fibrosis?
Suzy is a 14 year old with pulmonary fibrosis. This disease causes progressive scarring of the...
Suzy is a 14 year old with pulmonary fibrosis. This disease causes progressive scarring of the lungs and therefore, reduced inspiratory volumes and chronic hypoxemia. Suzy is very inquisitive. Due to her disease, she knows that when she breathes in, her lungs help to bring oxygen into her blood, and when she breathes out, she gets rid of carbon dioxide from her blood. At her appointment today, you note that she has cyanosis (blue coloration) and clubbing in her fingers...
A patient with Duchenne muscular dystrophy presents with fibrosis, where some of the contractile muscle fibers...
A patient with Duchenne muscular dystrophy presents with fibrosis, where some of the contractile muscle fibers are replaced with scar tissue, although the nervous system and neuromuscular junction are not altered. In this patient the sarcomere length, muscle belly length, and fiber type distribution are equivalent to a control subject. A. What would be the predicted change in maximum isometric force and maximum unloaded shortening velocity compared to a control subject. Describe using terms of muscle architecture (sarcomere arrangement- parallel...
the role of surfactant in lung disease and host defense against pulmonary infection /with in citation...
the role of surfactant in lung disease and host defense against pulmonary infection /with in citation and references .
Cystic fibrosis is caused by a mutation in a single gene. Homozygotes for this mutant recessive...
Cystic fibrosis is caused by a mutation in a single gene. Homozygotes for this mutant recessive allele (ff) have cystic fibrosis. Within a population, 2% of people have cystic fibrosis. Assuming Hardy-Weinberg equilibrium, the frequency of heterozygotes in the population is 0.24. If inbreeding was common in this population, what would happen to the percentage of people who have cystic fibrosis over time?
Cystic fibrosis is a rare disease caused by homozygosity for a recessive allele, and characterized by...
Cystic fibrosis is a rare disease caused by homozygosity for a recessive allele, and characterized by a build-up of mucus in the lungs and difficulty breathing. A woman whose maternal uncle had the disease is trying to determine the probability she and her husband could have an affected child. Her husband's sister died of the disease. Assuming the uncle and the sister are the only family members who had the disease, what is the chance that the couple's first child...
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT