Muscle Flashcards

1
Q

Where is skeletal muscle derived from?

A

Mesodermally derived myogenic stem cells give rise to myoblasts.

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2
Q

Explain why skeletal muscle initially has centrally positioned nuclei and then where these nuclei move to.

A

Myoblasts fuse to produce a primary myotube. The nuclei are then gradually displaced to the periphery by the newly synthesised actin/myosin micro filaments.

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3
Q

What is the difference between red and white skeletal muscle fibres?

A

Red muscle fibres fatigue slower and can do many repeated repetitions whilst white muscle fibres fatigue quickly but they are faster and stronger (for sprinting).

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4
Q

What is a myotendious junction?

A

These is the junction between muscle and the collagen of tendons. Sarcolemma lies between the muscle fibres and the tendon collagen.

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5
Q

Where would u find the perimysium? What is it’s function?

A

This is found surrounding a fasicle (bundle of muscle fibres) in a muscle. It carries nerves and blood vessels.

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6
Q

What is the name of the membrane which surrounds an individual muscle fibre?

A

Endomysium.

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7
Q

What two muscle types does the tongue have and what is their function?

A

Intrinsic which change the shape of the tongue and extrinsic which moves the position of the tongue within the mouth.

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8
Q

What accounts for the mobility and flexibility of the tongue?

A

Multidirectional muscle fibres. Also plasticity and strength of the connective tissue assists with this.

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9
Q

Describe the banding pattern in skeletal muscle.

A

MHAZI. The A line is found within the H zone of the M band, and the I band is found within the Z disc.

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10
Q

What is a sacromere?

A

This is one muscle unit which is the same length as a muscle fibre.

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11
Q

What is seen when skeletal muscle is cut transversely?

A

Micro fibrils can be seen as dots.

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12
Q

Where in skeletal muscle are mitochondria found and how can they be seen on a stained section?

A

Mitochondria are between myofibrils and are seen as purple streaks.

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13
Q

What three substances are thin filaments of muscle composed of?

A

Actin, tropomyosin and troponin.

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14
Q

What is a good clinical marker for cardiac muscle damage?

A

Troponin is released from ischaemic heart muscle, small changes indicate damage to cardiac muscle but levels are not proportional to the damage.

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15
Q

Describe the structure of a thick muscle filament.

A

These are made from myosin molecules. These have a long tail and 2 heads. The heads protrude from the sides. Of the bundle of myosin molecules.

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16
Q

Actin molecules form a helix structure. What other molecules are involved in thin filaments?

A

Tropomyosin molecules wrap around this to stabilise the structure, and to each of these a troponin complex attaches.

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17
Q

What can be said about the thick filaments in the centre of the sacromere (the M line)?

A

Here there are no myosin heads because they point outwards to where the actin molecules are present.

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18
Q

What is the role of calcium in activating muscle contraction?

A

Calcium binds to the TnC of the troponin complex and this causes a conformational change and the tropomyosin molecule moves away from actins binding sites. This allows myosin to bind and contraction begins.

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19
Q

What is the role of ATP in muscle contraction?

A

When ATP binds to the myosin filament this releases the actin molecule. Hydrolysis of ATP leads to movement of this head and it cocks back. It then binds to another Troponin molecule.

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20
Q

What is rigor Mortis?

A

This is because there is no ATP and so the myosin head is not released from the troponin molecules and so the muscles are very stiff.

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21
Q

Where are T tubules found in skeletal muscle?

A

They are found at the join between the A and the I band. It is a triad in this type of muscle.

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22
Q

What are the two different types of muscle?

A

Striated and non-striated.

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23
Q

What is a neuromuscular junction?

A

This is a small terminal swelling on an axon which contain vesicles of acetylcholine.

24
Q

What is the action of acetylcholine?

A

This binds to receptors on sarcolemma and initiates an action potential which propagates along the length of the muscle.

25
Q

Explain how a nerve impulse leads to muscle contraction.

A

The nerve impulse stimulates release of acetylcholine which leads to depolarisation of sarcolemma and voltage gated sodium channels open. This causes a change in voltage sensor proteins of t tubules which leads to opening of calcium channels. Calcium is released into sarcoplasm.

26
Q

Describe features of cardiac muscle that allow us to differentiate it from skeletal muscle.

A

It has centrally positioned nuclei, and it branches. It also has intercalating discs for electrical and mechanical coupling.

27
Q

What is a adherents type junction?

A

These are found in cardiac muscle and are for actin anchorage.

28
Q

Are there myofilaments in cardiac muscle?

A

No, there are only actin and myosin molecules.

29
Q

Where do T tubules lie in cardiac muscle?

A

They lie along Z bands. Here they are dials and the proximity of this to the sarcoplasmic recticulum allows calcium release for muscle contraction.

30
Q

What can be said about the contraction of cardiac cells?

A

It is spontaneous rhythmic contraction. Potentials are generated by the SAN and AVN.

31
Q

What are the distal conducting cells called in the heart and what is important about their structure?

A

They are called purkinje fibres. They have abundant glycogen, sparse myofilaments and e tensile gap junctions which all allow for rapid contraction.

32
Q

State the most common location where smooth muscle is found.

A

Contractile walls of vessels such as the gut.

33
Q

What shape are smooth muscle cells?

A

They are spindle shaped with central nuclei.

34
Q

How do contractions of smooth muscle compare to those of striated muscle?

A

They are much slower and sustained and the muscle can remain contracted for days. This means they are capable of being stretched.

35
Q

Where are myoepithelial cells found?

A

They are found around secretory units of some exocrine glands so assist in secretion through ducts. They are also present in the ocular iris and dilate the pupil.

36
Q

What is a myofibroblast cell?

A

These are found at wound healing sights and are responsible for collagen secretion but also contraction.

37
Q

How is smooth muscle in the gut innervated?

A

It is innervated by the autonomic nervous system which stimulates release of neurotransmitters.

38
Q

Explain how the contraction of smooth muscle is different to that of skeletal muscle.

A

Smooth muscle has thick and thin filaments in a diagonal arrangement, and this leads to a twisting contraction motion. Intermediate filaments are attached to dense bodies which are scattered throughout the sarcoplasm.

39
Q

How do cells in smooth muscle repair?

A

These cells retain their mitotic capability and so they form new smooth muscle.

40
Q

Explain the consequences of cardiac muscle becoming damaged.

A

Cardiac muscle is unable to regenerated and therefore once it is damaged it is not replaced. This can lead to heart failure if it no long has sufficient contraction.

41
Q

Explain how hyperplasia and hypertrophy occur in skeletal muscle.

A

Skeletal muscle does not have mitotic capability, however new cells are produced by satellite cells. This leads to hyperplasia (increase in cell number) and hypertrophy (increase in cell size).

42
Q

How often does muscle remodelling occur?

A

This is a continuous process with myosin and actin molecules being replaced once every two weeks.

43
Q

When muscle destruction is higher than replacement what is this called?

A

Atrophy.

44
Q

What is the metabolic adaption of muscles caused by increased exercise?

A

With increased exercise the SR swells and there is an increase in mitochondria abundance. This means more ATP is produced which leads to increased T tubule density and increased contractile proteins.

45
Q

What is the difference between high resistance exercise and endurance exercise on muscles?

A

High resistance exercises lead to hypertrophy whilst endurance exercises lead to an increase in endurance due to stimulated mitochondrial synthesis and vascular changes.

46
Q

What is a side effect of disuse atrophy?

A

Disuse atrophy is where there is loss of protein and therefore muscle mass due to disuse. This has an impact on thermoregulation and can lead to hypothermia in severe cases.

47
Q

What is Denervationatrophy?

A

This is where loss of motor neuron lesions leads to weakness and muscle atrophy.

48
Q

How can muscle length be changed?

A

Sustained stretching can increase the length of muscles. Immobilisation reduces muscle length.

49
Q

What is myasthenia gravis?

A

This is autoimmune destruction of the end plates Ach receptors or loss of junctional folds at the end plate.

50
Q

What are the symptoms of myasthenia gravis?

A

Someone suffering from this will find it hard to maintain muscle contraction. They may have drooping eyelids and double vision.

51
Q

What enzyme is responsible for the breakdown of ACh?

A

Acetylcholinesterase.

52
Q

What is duchennes?

A

Duchennes is a form of muscular dystrophy, as there is a lack of the molecule dystrophin.

53
Q

What is pseudo hypertrophy?

A

This is a condition which occurs as part of duchennes. The lack of dystrophin means that muscles tear themselves apart and then this leads to necrosis as calcium enters the cell. Swelling presents as pseudo hypertrophy before fat and connective tissue replaces the muscle.

54
Q

Why can contracture occur in duchennes?

A

This can occur because there is an imbalance in muscle pairs.

55
Q

What is malignant hyperthermia?

A

It is when someone is given general anaesthesia or a similar drug and this leads to an opening in the calcium channels. This leads to an increase in calcium concentration which causes muscles to contract. This use of ATP stimulates more synthesis and their causes an excessive amount of heat.