What is myasthenia Gravis? Describe what part of neuromuscular junction is impacted and how that is associated with the presentation of the patient. The drug neostigmine is used to both diagnose and treat MG. How does it work and what is its target?
Ans. Myasthenia gravis (MG) is the most commonly encountered autoimmune disease of the neuromuscular junction. MG causes fluctuating weakness that worsens with activity and as the day progresses, and ocular weakness, causing ptosis and diplopia.
Patients with MG present with painless, specific muscle weakness, and not generalized fatigue. Myasthenic weakness typically affects the extraocular, bulbar, or proximal limb muscles. Droopy eyelids or double vision is the most common symptom at initial presentation of MG, with more than 75% of patients.
Neostigmine works by slowing the breakdown of acetylcholine when it is released from nerve endings. This means that there is more acetylcholine available to attach to the muscle receptors and this improves the strength of your muscles.
What is rigor mortis? What causes it? How long does it last?
Rigor mortis is when the muscles lock up post-mortem. It is the third stage of death. It occurs 4–6 hours after death.
The mechanism of rigor mortis is based on sustained contraction of the muscles of the body following death. This happens because inasmuch as ATP is required for contraction, it is equally needed for the muscles to relax. So, in the absence of ATP, there would be no relaxation of the contracted muscles.
The muscle stiffening usually starts from the facial muscles and ends with the diaphragm. The entire process lasts for 54 hours. Hence after 54 hours, the stiffness of the body (rigor mortis) should have disappeared.
Ans 31. The prime mover of inspiration is the (a) diaphragm, (b) internal intercostals, (c) external intercostals, (d) abdominal wall muscles
Ans 32. The muscles of the abdomen are made up of the muscles of the anterolateral abdominal wall and the muscles of the posterior abdominal wall. These muscles work together to protect the internal organs (viscera) by covering them completely. They also help to provide postural support, assist in forceful expiration and increase the intra-abdominal pressure.
The anterolateral abdominal wall consists of four layers- skin, superficial fascia (connective tissue), muscles and parietal peritoneum. The muscles of the anterolateral abdominal wall include flat and vertical muscles. The flat muscles are stacked on top of each other and have fibres that run in different directions, helping to strengthen the abdominal wall. There are two vertical muscles in the anterolateral abdominal wall, and these are situated near the midline of the body. The posterior abdominal wall is made up of the lumbar vertebrae, pelvic girdle, five posterior abdominal muscles and their associated fascia. Major nerves, vessels and organs are located on the inner surface of the posterior abdominal wall. The posterior abdominal wall is found medial to the lateral abdominal walls and is limited anteriorly by the posterior part of the parietal peritoneum.
The white line (Latin: linea alba) is a fibrous structure that runs down the midline of the abdomen in humans and other vertebrates. In humans linea alba runs from the xiphoid process to the pubic symphysis. The name means white line and the linea alba is indeed white, being composed mostly of collagen connective tissue.
33. Draw and describe the anterior triangle. What are its boundaries? Contents.
The anterior triangle is situated at the front of the neck. It is bounded:
The contents of the anterior triangle include muscles, nerves, arteries, veins and lymph nodes.
34. Draw and describe the posterior triangle. What are its boundaries? Contents.
Ans. The posterior triangle has the following boundaries:
Apex: Union of the sternocleidomastoid and the trapezius muscles at the superior nuchal line of the occipital bone
Anteriorly: Posterior border of the sternocleidomastoideus
Posteriorly: Anterior border of the trapezius
Inferiorly: Middle one third of the clavicle
Roof: Investing layer of the deep cervical fascia
Floor: (From superior to inferior)
1) M. semispinalis capitis
2) M. splenius capitis
3) M. levator scapulae
4) M. scalenus posterior
5) M. scalenus medius
Contents
A) Nerves and plexuses:
B) Vessels:
C) Lymph nodes:
D) Muscles:
35. Name the four muscles that form the rotator cuff of the shoulder. Use the acronym?
Ans. The acronym SITS is often used as the name for the collection of four muscles that make up the rotator cuff: supraspinatus, infraspinatus, teres minor, and subscapularis
36. Where is the femoral triangle located? Name the boundaries (SAIL). Name the contents (NAVY)
Ans. The femoral triangle (or Scarpa's triangle) is an anatomical region of the upper third of the thigh. It is a sub fascial space which appears as a triangular depression below the inguinal ligament when the thigh is flexed, abducted and laterally rotated.
The borders of the femoral triangle can be remembered using the word , SAIL expanded as
Lateral border: Sartorius (S)
Medial Border : Adductor Longus (A)
Base border: Inguinal Ligament (IL)
The contents of the Femoral triangle is abbreviated as NAVEL:
Femoral Nerve (N)
Femoral Artery (A)
Femoral Vein (V)
Femoral Canal (Empty space) (E)
Lymphatics (L)
37. Botulism is an acute neurologic disorder that causes potentially life-threatening neuroparalysis due to a neurotoxin produced by Clostridium botulinum. The toxin binds irreversibly to the presynaptic membranes of peripheral neuromuscular and autonomic nerve junctions.
Botulinum toxin, one of the most lethal biologic toxins, is produced by the bacteria Clostridium botulinum. It acts at the neuromuscular junction, where it binds to the presynaptic cholinergic terminal and inhibits the release of acetylcholine. This functional denervation causes weakness and atrophy
What is myasthenia gravis? Describe what part of the neuromuscular junction is impacted and how that...
6. Draw the Neuromuscular junction and label the Following structures. Include the three substances that interfere with normal muscle contraction (both toxic and therapeutic). ID synapse, neurotransmitter synaptic cleft, axon terminal, synaptic bulb, synaptic vesicles, motor end plate, acetylcholine receptors, Junctional folds, acetylcholinesterase. 7. Describe or draw each of the contractile proteins (actin/myosin) and regulator proteins (troponin & tropomyosin). Explain the set up and how each participate in muscle contraction. Name the protein that attaches the sarcomere to the sarcolemma...
1. A. Name the three planes and the positions they each describe to identify a unique position in the human body. B. Name the two major ventral body cavities plus the major organs found in them. C. Name the cavities that the heart and lungs reside in. D. Finally, list the six levels of organization in nature. 2. A. Describe the three components of an atom in terms of charge and location. Define atomic mass and atomic number. B. For...
1. According to the paper, what does lactate dehydrogenase
(LDH) do and what does it allow to happen within the myofiber? (5
points)
2. According to the paper, what is the major disadvantage of
relying on glycolysis during high-intensity exercise? (5
points)
3. Using Figure 1 in the paper, briefly describe the different
sources of ATP production at 50% versus 90% AND explain whether you
believe this depiction of ATP production applies to a Type IIX
myofiber in a human....
change pas channels in the volta t ive protein to change shape. This A of the S l e terminal siste oplasmic reticum calcio p r eneule warcoplasm reticulum sodium ions m o nster transverse tubules sarcolemma: calcium ions Saroplasmic reticum: triadsarcolemma: calcium ions sons bind to This causes a change in shape and exposing C D E Calcium vesicle tylcholine action potential Sodium sarcolemma calcium on myosin heads Sodium sacoplasmic reticulum calcium ions actin 15. An attaches to exposed...