Muscular Dystrophy Experiment

Improved Essays
Muscular dystrophy is a hereditary disease that causes the muscles in your body to weaken, and become wasted. It is a rare disease that affects 20,00 to 200,00 United States citizens per year. It can have life lasting effects on the ones infected. The Department of Medicine/Cardiology, at the University of Minnesota Medical School did a study on prevention for the most common fatal form of muscular dystrophy, Duchenne Muscular Dystrophy. Duchenne Muscular dystrophy is caused by an absence of a protein that keeps muscles in tact, dystrophin. Dystrophin is the protein responsible for connecting the internal cytoskeleton and the extracellular matrix. It acts as a protectant against the sarcolemmal membranes contractions. It affects 1 in every …show more content…
For the experiment they used mice because they have a lower PCr/ATP ratio compared to humans, which would show what a DMD patient would be going through. At the University of Minnesota School of Medicine they conducted an experiment with six control mice and nine mdx mice. They had 3 males and 3 females weighing in at 28-38 grams. They range from 22-28 weeks old. The nine mdx mice were 3 male and 6 female. Their weights were from 27-31 grams, and were 22-28 weeks in age. To start the experiment the mice were induced with a 2% isoflurane and a 3% mixture of isoflurane, and a 1:1 mixture of of oxygen and N2O. The animal ventilator they used scanned their heart rate, body temperature, and respiration rate. The mices body temperature was maintained about 37 degrees. They had a high temperature water system and a fan. They tested the mice with coils to make them have the problem. They performed MRI’s on the mice. The hearts were scanned using the 3D-ISIS. After they examined the hearts they froze them in liquid nitrogen immediately after they extracted it from the mouse’s body. They than crushed and weighed the hearts. ATP was then extracted from the tissue. They than mixed a sample of chloroform and saturated phenol, than they were centrifuged at 10,000xg for 5 minutes. After the

Related Documents

  • Decent Essays

    The Daphnia Puplex

    • 163 Words
    • 1 Pages

    In this experiment the Daphnia will be observed, checking the heart and circulatory system under low power magnification. Daphnia can be found…

    • 163 Words
    • 1 Pages
    Decent Essays
  • Improved Essays

    A special type of synthetic tissue is then cut up by suregons and sewn to the atora (artery to the body) and the pulmonary artery (artery to the lungs) This synthetic is used to help connect the artificial heart to the remaning parts the natural heart. The artificial heart is then placed into the chest and connected by quick connects which are similar to little snaps. Once this has all been sucsessfuly completed the patient is taken off th Heart-lung machine and the surgical team checks that heart is working…

    • 576 Words
    • 3 Pages
    Improved Essays
  • Improved Essays

    Duchenne muscular dystrophy (DMD), the most common form of all muscular dystrophies, is an X-linked disorder affecting approximately one in 5000 newborn boys. " (page1; paragraph 1; lines 1-4)" Patients are usually restricted to a wheelchair around the age of twelve and facing death somewhere between the ages twenty-five to thirty. DMD is caused when the dystrophin gene is mutated. That mutation stops the communication for a functional protein.…

    • 533 Words
    • 3 Pages
    Improved Essays
  • Superior Essays

    Duchenne muscular dystrophy (DMD) is a one type of muscular dystrophy. Muscular dystrophy is a group of genetic disorders, leading to progressive muscle degeneration. People suffering from most common muscular dystrophies ,Duchenne/Becker (DMD), Myotonic (MMD), and Limb-Girdle (LGMD), experience muscles degradation overtime, leading to overall muscle weakness and decreased mobility. Statistics show that the most prevalent forms of muscular dystrophy are rare.…

    • 806 Words
    • 4 Pages
    Superior Essays
  • Improved Essays

    The protein that was concluded was dystrophin. The disease that is associated with this protein is Duchenne. Duchenne is referred to as DMD and is associated with muscular dystrophy. DMD is one of the most common gene malfunctions and is causes by having a problem with a gene which makes up the dystrophin protein. Gupta (2014) explained that when the protein is functioning properly, muscle cells are able to keep their shape and strength, but without it they can begin to break down and become weaker over time.…

    • 372 Words
    • 2 Pages
    Improved Essays
  • Improved Essays

    MDA Research Paper

    • 467 Words
    • 2 Pages

    MD is a disease that weakens your muscles and stops you from doing more things. I believe that scientists should work on finding a cure or do something to help for people with MD. If you help donate to Muscular Dystrophy Association you could help make more medicine to help people with MD. I will be talking about how MDA has events, about the association and what MD is. MDA holds a lot of events such as 5k walks/runs to help raise money for the people suffering this disease.…

    • 467 Words
    • 2 Pages
    Improved Essays
  • Decent Essays

    Dystrophin is a protein that is located in muscles that work with movement. The job of Dystrophin is to produce muscle proteins that protects the skeletal, cardiovascular and nervous system. Dystrophin plays an important role in protein complex that work together to strengthen muscle fiber and help prevent injuries. It also plays a role in cell signaling between proteins and chemical signals. However its main job is connecting and weighing down each structural framework between proteins and molecules outside the cell.…

    • 277 Words
    • 2 Pages
    Decent Essays
  • Improved Essays

    Muscular Dystrophy Muscular Dystrophy is a group of disorders characterized by a progressive loss of muscle mass and consequent loss of strength. There are multiple types of muscular dystrophy, each type affecting a different part of the body. Examples would be Duchenne muscular dystrophy, which effects toddlers starting from their third birthday and causing them to be in a wheel chair by the time they are 12 and usually dying from respiratory failure in their late twenties, early thirties. Becker muscular dystrophy is similar to Duchenne, it just starts later on in life and has a slower attack, most die in their mid forties.…

    • 530 Words
    • 3 Pages
    Improved Essays
  • Superior Essays

    Duchenne MD

    • 1444 Words
    • 6 Pages

    Effects Powerful Enough To Deteriorate Muscle And Hope Need an attention-getter. In 1861, Guillaume Benjamin Amand Duchenne wrote De L'électrisation Localisée in which he described the disorder now referred to as DMD. Although later discovered, Edward Meryon described this genetic disease first, but by that time it had the title of “Duchenne” (Abramovitz p. 19-21). Out of nine different types (“Duchenne”), Duchenne MD, the most common of childhood muscular dystrophies (Abramovitz p. 19-21), is known as the second largest gene.…

    • 1444 Words
    • 6 Pages
    Superior Essays
  • Great Essays

    160116 Duchenne Muscular Dystrophy “Muscular dystrophy (MD) is a genetic disease characterized by progressive weakness and degeneration of the skeletal or voluntary muscles which control movement” (Muscular dystrophy, 2013). Muscular dystrophy is classified into nine major types that each affect specific muscle groups, certain age groups and are identified by different signals. Duchenne muscular dystrophy most commonly affects males and is targeted at younger children (Facts about Muscular Dystrophy, 2015). “The Centers for Disease Control and Prevention estimated that 1 out every 5,600 to 7,700 males between the age of 5-24 has DMD” (Seiner, Duchenne Muscular Dystrophy).…

    • 1194 Words
    • 5 Pages
    Great Essays
  • Improved Essays

    Echo Intensity Paper

    • 982 Words
    • 4 Pages

    Lamminen et al., examined 24 healthy children and 20 children with NMDs. All children with muscular dystrophy had clearly abnormal US images with increased echogenicity, and the majority of images from children with benign myopathic disorders had higher echogenicity as well. Many studies similar to this have shown higher echogenicity in children with NMDs, making US an easy method of examining these disorders. However, EI values are arbitrary and specific to the US model being used (Pillen et al., 2009). For this reason, EI values from US imaging cannot properly be used as a clinical measurement at this…

    • 982 Words
    • 4 Pages
    Improved Essays
  • Superior Essays

    Duchenne’s muscular dystrophy Duchenne’s Muscular Dystrophy Zachary Uecker Genetic Disease Abstract Duchenne’s muscular dystrophy is a genetic disease that targets skeletal muscles and over time, the muscles lose protein and are replaced by fats and connective tissue, making the skeletal muscles unusable. In this paper, the parts of Duchenne’s that will be covered are the method of transmission, statistics about Duchenne’s in the population, the pathophysiology, the body systems effected, signs and symptoms, age of onset, treatment/therapy options, psychological factors, prognosis, prevention techniques, ethical considerations, and how genetic counseling may be utilized for patients.…

    • 1182 Words
    • 5 Pages
    Superior Essays
  • Improved Essays

    Mutations in the DMD gene, which creates dystrophin, causes Muscular dystrophy. Dystrophin is located in the skeletal and and cardiac muscles. Alterations or mutations in the gene make it so little to know dystrophin are produced, causing Muscular Dystrophy. Without enough dystrophin muscles contract and get damaged. (2015)…

    • 341 Words
    • 2 Pages
    Improved Essays
  • Improved Essays

    Muscular Dystrophy Essay

    • 1251 Words
    • 5 Pages

    This disorder affects muscle tissues, leading to problems with organs. Rarely will affected individuals live past their late twenties. (Morgenroth, Hache, and Clemens, 2012) Dystrophin is part of the dystrophin-associated glycoprotein complex (a protein complex) that plays the role of an anchor, linking every muscle…

    • 1251 Words
    • 5 Pages
    Improved Essays
  • Improved Essays

    Frank James is a 72 year old male who was admitted in the ward due to the exacerbation of his heart failure. His condition dramatically worsened, having developed pulmonary oedema as depicted by bat wings on his chest x-ray as well as signs and symptoms of cardiogenic shock. Vital assessment tools in identifying and prioritising the nursing care for Frank consist of the ABCDE of primary survey in conjunction with physical examination (inspection, palpation, percussion, and auscultation). This case study will explore relevant nursing assessments such as primary survey, physical examination, and the pathophysiology of cardiogenic shock and how it relates to Frank’s presenting signs and symptoms. Primary survey which incorporates airway, breathing,…

    • 510 Words
    • 3 Pages
    Improved Essays