Human Musculoskeletal Anatomy Flashcards

1
Q

What 3 layers make up skeletal tissue?

A

Ectoderm, mesoderm and endoderm

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2
Q

What is connective tissue?

A

Tissue that connects and support organs and other tissues

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3
Q

Cartilage
- properties (4 marks)
- What is it made up of (2 marks)

A
  • Made from chondrocytes embedded in a matrix
  • No blood vessels within cartilage so nutrients and oxygen must diffuse through the matrix in the cell (therefore doesn’t heal well)
  • Hard, flexible, compressible and elastic
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4
Q

Describe the three types of cartilage and order them from weakest to strongest

A
  • Hyaline cartilage is located at the ends of the bones, the nose and trachea. High proportion of collagen. Weakest
  • Yellow elastic cartilage. Contains yellow elastic fibres located in external year. Chondrocytes surrounded by network of elastin fibres,
  • White fibrous cartilage. Strongest. Many bundles of collagen. Great tensile strength and found between vertebrae
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5
Q

What does the compact bone matrix consist of?
(2 marks)

A
  • 30% organic (mainly protein collagen to resist fracture)
  • 70% inorganic (mainly hydroxyapatite containing calcium and phosphate to prevent compression)
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6
Q

Describe Haversian systems (osteons) and how it provides a transport system in the bone
(3 marks)

A
  • Haversian canal at the centre of the system contains an arteriole, venule, lymph vessels and nerve fibres
  • Lamellae concentric rings of hydroxyapatite around the lamellae
  • Lacunae containing osteoblasts and osteoclasts. Nourished by diffusion through tissue fluid. Link to other cells via canaliculi channels.
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7
Q

What are osteoblasts and osteoclasts?

A
  • Osteoblasts build lamellae up by secreting/deposit hydroxyapatite /calcium salts. Bone is reformed by osteoblasts
  • Osteoclasts continually breakdown/reabsorb bone compounds/lamellae for rebuilding
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8
Q

What is the cause, symptoms and treatment for rickets (children) / Osteomalacia (adult)

A

Cause
- Deficiency in vitamin D (from butter, eggs, liver and synthesised by the skin), which leads to the inability to absorb calcium from the gut leading to defective calcification of bone
Symptoms
- Bone tenderness, fractures and skeletal deformities
Treatment
- Calcium and vitamin D supplements

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9
Q

What is the cause, symptoms and treatment for brittle bone disease?

A

Cause
- Inherited caused by a mutation in the gene for collagen. Causes an imbalance between the organic and inorganic components of bone matrix
Symptoms
- Loose joints, poor muscle tons and susceptibility to fractures
Treatment
- Drugs to increase mineral density in bone, or surgery to place metal rods in long bones

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10
Q

What is the cause, symptoms and treatment for osteoporosis?

A

Cause
- Risk factors such as age, smoking, hormone imbalance following menopause, poor diet, illness or alcohol misuse
Symptoms
- Abnormally fast loss of bone density leading to fractures
Treatment
- Calcium and vitamin D supplements

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11
Q

Describe the ultrastructure of skeletal muscle / The level of organisation in skeletal muscle. (3 marks)

A
  • Skeletal muscle is made up of a bundle of fibres that are multinucleated, with a striated appearance
  • Bundles of fibres are made up of fibres, which are made up of many myofibrils
  • Myofibrils contain actin and myosin myofilaments arranged in repeated sarcomeres
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12
Q

Describe the different striations/bands in sarcomeres
(5 marks)

A
  • Z line end of sarcomere where actin filaments are joined
  • I band x 2 are actin only
  • A band is the whole length of the myosin filament. Overlaps in dark areas with actin
  • H band is myosin only
  • M line is the centre of the sarcomere where myosin molecules are attached
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13
Q

Describe the structure of actin
(3 marks)

A
  • Two twisted chains of actin monomers, with myosin head binding sides
  • Protein tropomyosin is wrapped around the actin fibre. Tropomyosin blocks the binding site
  • Troponin found at positions along the fibre
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14
Q

Describe the structure in myosin
(2 marks)

A
  • Many myosin molecules
  • Two heads with ATPase activity, which project from the surface
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15
Q

Describe the sliding filament theory for muscle contraction
(8 marks)

A
  1. Nervous impulse causes calcium ions to be released from the sarcoplasmic reticulum
  2. Calcium ions bind to troponin and change the shape of the troponin molecule
  3. Tropomyosin moves, exposing the myosin binding site on the actin
  4. Myosin heads can form cross bridges to actin
  5. ADP and Pi attached to the head are released changing the myosin head shape as it bends, pulling the actin past myosin aka the power stroke
  6. Cross bridge is broken as ATP attaches to myosin head
  7. ATP is hydrolysed for energy for the head to bind to actin again
  8. Process continues until calcium ions is actively pumped back into the sarcoplasmic reticulum
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16
Q

How are slow twitch muscle fibres characterised by?
(6 marks)

A
  • Aerobic respiration
  • Contract for a longer time
  • Fatigue slowly
  • Rich blood supply
  • High numbers of mitochondria
  • High myoglobin
17
Q

How are fast twitch muscle fibres characterised by?
(3 marks)

A
  • Anaerobic respiration for ATP
  • Short bursts of strength/speed
  • High tolerance to lactic acid
18
Q

Anaerobic respiration results from a lack of oxygen. Describe the two methods muscles use to deal with this.

A
  1. Creatine phosphate
    - Store of phosphate for the rapid phosphorylation of ADP to ATP when oxygen levels are insufficient for oxidative phosphorylation. It lasts for 6 seconds
  2. After creatine phosphate, glycolysis supplies ATP. This also creates lactic acids that builds up causing fatigue and muscle cramp.
19
Q

Describe the energy sources in the muscles
(3 marks)

A
  • Glycogen stored in muscles is main source of energy during muscle contraction. Releases glucose only for respiration
    2. Carbohydrate loading increases muscle glycogen stores
    3. Protein may be used as an energy source
20
Q

What is the function of the skeleton?
(5 marks)

A
  • Support the body
  • Protect vital organs
  • Provide a site for muscle attachment
  • Store calcium
  • Produce red blood cells
21
Q

What are the parts of the axial skeleton?
(4 marks)

A
  • Skull
  • Vertebral column
  • Sternum
  • Ribcage
22
Q

What are the parts of the appendicular skeleton?
(4 different parts)

A

Pectoral girdle
- Clavicle (collar bone)
- Scapula (shoulder blade to rear)
Fore limb
- Humerus
- Ulna
- Radius
Pelvic girdle
Hind limb
- Femur
- Tibia
- Fibula

23
Q

What is the definition of a fracture?

A

Break in bones caused by high impact or stress. Could also have resulted from a medical condition that weakens bones.

24
Q

What are fractures always caused by?

A

When the physical force on the bone is greater than the strength of the bone

25
Q

Describe the 5 different type of fractures

A
  • Simple > Skin over bone remains intact
  • Compound > Bone penetrates skin or internal organs
  • Comminuted > Bone is fragmented into several pieces
  • Non-displaced > Bone is not moved from original position
  • Displaced > Bone is moved from original position
26
Q

What the treatments used to treat fractures
(2 marks)

A
  • Realignment of the bone and immobilisation using a splint or a cast. This gives time for osteoblasts to produce new bone and for osteoclasts to remodel the bone
  • Plates/pins may be inserted during surgery to further support the bone
27
Q

What is the function of the vertebral column?

A
  • Supports the body so that it is flexible and allows bending/twists
  • Protection for the spinal cord
28
Q

What are the 3 vertebrae, how many of each are there and describe there shape/morphology.

A
  • Cervical (7) Wider vertebral canal. Vertebroarterial canal carries blood vessels to brain. Smaller as they bear less weight
  • Thoracic (12) Articulate with the ribs. Large transverse processes
  • Lumbar (5) Largest vertebral bodies. Provide support to the body and absorb stress of lifting and carrying