Muscle Contraction, Tissue and Plasticity etc Flashcards

1
Q

What are the structures and functions of smooth muscle?

A
  • Involuntary.
  • It’s found in the walls of your hollow internal organs such as your gut, blood vessels and uterus.
  • Mononucleated and spindle shaped.
  • Contract slowly and don’t fatigue.
  • Regulated by the autonomic nervous system.
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2
Q

What are the structures and functions of cardiac muscle?

A
  • Not a true syncytium
  • Myogenic
  • Made of muscle fibres connected by intercalated disks.
  • Mononucleated and cross striated.
  • Contract rhythmically and don’t fatigue.
  • Central nuclei.
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3
Q

What are the structures and function of skeletal muscle?

A
  • Voluntary.
  • Regular cross-striations.
  • Force production for locomotion and breathing.
  • Force production for postural support.
  • Heat production during cold stress.
  • Largest protein store in the body.
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4
Q

How are skeletal muscle fibres arranged? ( connective tissue covering)

A

Each fibre is arranged in bundles called fascicles:

  • Epimysium surrounds entire muscle
  • Perimysium surrounds fascicles
  • Endomysium surrounds individual muscle fibres
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5
Q

What are 3 functions of connective tissue covering?

A
  • Protective role
  • Fibrosis
  • Collagenisation
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6
Q

What is the microstructure of the skeletal muscle?

A
  • Sarcolemma ( muscle cell membrane)
  • Myofibrils ( tubular structures that pack the fibres)
  • Myofilaments ( threadlike strands within myofibrils)
  • Actin (thin filament) troponin and tropomyosin
  • Myosin (thick filament)
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7
Q

What occurs during muscle contraction?

A

1) Depolarisation from the sarcolemma -> T tables -> Sarcoplasmic reticulum causes release of Ca2+ ions into the sarcoplasm.
2) Calcium ions bind to troponin causing a conformational change and the actin-myosin binding site is exposed.
3) Calcium ions activate ATPase which breaks ATP down which is used to move the myosin head.
4) ATP also provides energy to break the actin myosin cross bridge.

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8
Q

What 3 complexes is troponin compromised of?

A

Troponin T: attaches to tropomyosin.
Troponin I: binds to actin head
Troponin C: captures Ca2+ and undergoes a conformational change that lifts tropomysin away from the actin filament.

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9
Q

Define excitation contraction coupling

A

It is a way to link muscle excitation (the depolarisation of the action potential) to Ca2+ release from the sarcoplasmic reticulum.

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10
Q

Explain excitation contraction coupling

A

1) Acetylcholine is released by the axonal ending, diffuses to the muscle cell, and attaches to the ACh receptors on the sarcolemma.
2) Depolarisation occurs, and the action potential is generated along the sarcolemma.
3) The action potential, carried deep into the cell via T tubules, causes the sarcoplasmic reticulum to release calcium ions.
4) The calcium concentration at the myofilaments increas; the myofilaments slide past one another, and the cell shortens.
5) After the action potential ends, calcium concentration at the myofilaments decreases.
6) The muscle cell relaxes and lengthens.

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11
Q

What are the 3 types of muscle fibre types?

A

Type I fibres- slow twitch and slow oxidative.
Type IIa fibres- intermediate and fast-oxidative glycolytic fibres.
Type IIb fibres- fast twitch and fast glycolytic fibres.

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12
Q

Define motor unit

A

A motor unit is made up of a motor neuron and the skeletal muscle fibers innervated by that motor neuron’s axonal terminals.

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13
Q

What is meant by motor unit recruitment and what order does it occur in?

A

Motor unit recruitment is a measure of how many motor neurons are activated in a particular muscle, and therefore is a measure of how many muscle fibers of that muscle are activated.
The higher the recruitment the stronger the muscle contraction will be. Motor units are generally recruited in order of smallest to largest ( slow to fast twitch) as contraction increases.

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14
Q

Define:

1) Hypertrophy
2) Hyperplasia
3) Atrophy

A

1) Cells getting bigger( increased number of myofibrils)
2) Increasing cell number
3) Cells getting smaller

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15
Q

How can mechanical stimuli produce cellular hypertrophy?

A

1) A mechanical stimulus comes in.
2) IGF1 and other compounds( ANG II) are produced by muscle fibres.
3) These compounds are fed back to the muscle fibre.
4) Satellite cells are then activated which then enter a cell and add a new nucleus.

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16
Q

What is a ligament?

A

They are bands of connective tissue which cross the joint space and therefore support and modify joint movement.
They join bone to bone.

17
Q

Describe the contents of ligaments

A
  • Classed as dense regular connective tissue.
  • Collagen fibres arranged in multiple directions, but not irregular like fascia.
  • Allows strength in multiple directions.
  • Very similar makeup to tendons, but:
    Usually have about 10% elastin content.
    More type III collagen.
  • 85% type I collagen plus other types to make up 75% of the dry weight.
  • 25% of dry weight is proteoglycans, glycoproteins, elastin and other proteins.
  • Like tendons, water content very important to functional properties.
18
Q

What are bursae?

A
  • Tough connective tissue sacs.
  • Contain synovial fluid.
  • Placed under areas of pressure.
  • Mainly under tendons near their insertion.
19
Q

What are tendon sheaths?

A
  • These are present where tendons cross joints.
  • Synovial fluid is secreted to lubricate the tendons over joints.
  • Blood supply in sheathed tendons is carried by the mesotenon where the sheath folds inwards.
20
Q

How can a muscle be injured externally and what are the consequences?

A

Can be caused by trauma or by injection which leads to severe necrosis of muscle fibres:

  • Torn plasmalemma leads to influx of Ca2+ leading to a necrotic zone.
  • Distal to the necrotic region the fibre is functionally denervated.
21
Q

Describe the major causes and consequences of myopathies in skeletal muscle.

A

Myopathy can occur in horses after exercise: cell membrane damaged, myoglobin is then released into the blood which can lead to renal failure.

22
Q

Describe the major causes and consequences of dystrophies in skeletal muscle.

A

Duchenne muscular dystrophy is a mutation in gene coding for the membrane protein dystrophin that occurs in humans, dogs and mice.
This leads to Degeneration/regeneration resulting eventually in failure of the respiratory muscles.

23
Q

Explain the role of satellite cells in the repair and regeneration of muscle fibres.

A

First, satellite cells( quiescent adult stem cells) are activated.
Then they migrate to a necrotic zone and form myotubes in a process similar to normal embryological development.

24
Q

Outline the effects of endocrine and nutritional factors in myopathies.

A
  • Nutritional:Primarily a condition found in herbivores due to selenium or vitamin E deficiency. Lambs and calves of deficent mothers are weak and have impaired movement.
  • Endocrine: Cushing’s disease, hypothyroidism and diabetes.
  • Both can lead to heart failure and renal disease.
25
Q

What are the two most common inflammatory conditions in dogs?

A
  • Polymyositis: Generalised inflammatory myopathy. Muscle damage is thought to the result of cell-mediated immunity.
  • Masticatory muscle myositis (MMM): focal inflammatory myopathy that selectively affects the muscles of mastication.
26
Q

Describe what is meant by sarcopenia.

A

Atrophy associated with raging is known as sarcopenia.

27
Q

What does HVPP stand for?

A

Equine Hyperkalemic Periodic Paralysis Disease.
This hereditary disease (autosomal dominant) affects horses under stress( training or racing.)
The horse undergoes a paralytic attack affecting most of the skeletal muscles.
HYPP is a sodium channelopathy- there is a single nucleotide change, which leads to a single amino acid change in the transmembrane ion channel.