Structure and Function of the MSK System – Muscles Flashcards

1
Q

Characteristics of skeletal muscles

A

Primarily involved in locomotion

Also involved in maintaining posture

Under voluntary control

Composed of muscle cells (muscle fibres)

Often known as striated muscle due to the appearance of the contractile proteins

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2
Q

Characteristics of smooth muscle

A

Lines structures including the stomach, intestines, and blood vessels

Primary function is to influence movement of material into, out of, and within the body

Involuntary muscle type

Non-striated – different arrangement of muscle cells compared to skeletal muscle

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3
Q

Characteristics of cardia muscle

A

Only found in the heart

Involuntary muscle type – moves blood through the circulatory system

Contraction of cardiac muscle regulated by the sinoatrial node

Striated structure – similar to skeletal muscle

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4
Q

Where is the origin of skeltal muscle found

A

Origin of a muscle is the end of the muscle that is attached closest to the trunk or to the more stationary bone

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5
Q

Composition of skeletal muscles

A

Skeletal muscle is a collection of muscle cells/muscle fibres

Each fibre is a long, cylindrical cell with up to several hundred nuclei near the surface

Skeletal muscle fibres are the largest cells in the body, formed by fusion of many individual embryonic muscle cells

Fibres lie in parallel arrangement, sheathed in connective tissue

Adjacent muscle fibres bundled together into units known as fascicles

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6
Q

How does growth and repair of skeletal muscle occur

A

Satellite (stem) cells activate & differentiate into muscle when needed for growth & repair

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7
Q

What do myofibrils consist of

A

several types of proteins organised into repeating contractile structures known as sarcomeres

Composed of thin and thick filaments

Proteins include:
Actin (thin filaments)
Myosin (thick filaments)
Tropomyosin & troponin (regulatory proteins)

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8
Q

What is actin

A

Actin makes up thin filaments of the muscle fibre

One actin molecule is a globular protein – usually multiple G-actin molecules polymerise to form long chains/filaments known as F-actin

In skeletal muscle, two F-actin polymers twist together like DNA creating thin filaments

Each G-actin molecule has a single myosin binding site and vice versa

Allows for cross-bridging of actin and myosin

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9
Q

What is myosin

A

Myosin makes up thick filaments of the muscle fibre

One myosin molecule is composed of two identical protein chains, each containing one large heavy chain and two smaller light chains

Phosphorylation of the light chains in skeletal muscle enhances contractile force

Heavy chains of myosin form the motor domain that uses ATP to create movement

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10
Q

What does a sarcomere consist of

A

Consists of thin & thick filaments in a repeating pattern of alternating light & dark bands

Z disks – zigzag protein structures, act as attachment sites for thin filaments

I bands – region occupied by thin filaments

A band – runs along the entire length of a thick filament, outer edges thick/thin overlap

H zone – region occupied by thick filaments

M line – proteins that act as attachment sites for thick filaments

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11
Q

What is muscle tension, load, contraction and relaxation

A

Muscle tension – force created by a contracting muscle

Load – weight or force that opposes muscle contraction

Contraction – creation of tension in a muscle, requires ATP

Relaxation – release of tension created by a contraction

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12
Q

How does muscle contraction occur at neuromuscular junction

A

Conversion of ACh signal from a somatic motor neuron into an electrical signal in MF

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13
Q

Explain excitation-contraction coupling

A

Muscle action potentials are translated into calcium signals

Calcium signals in turn initiate a contraction-relaxation cycle

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14
Q

Contraction-relaxation cycle

A

Sliding filament theory of contraction

One cycle is called a muscle twitch

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15
Q

4 major events in EC coupling

A

Ach is released from somatic motor neuron
Ach initiates action potential in muscle fibre
Triggers calcium release from sarcoplasmic reticulum
Calcium combines with troponin to initiate contraction

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16
Q

How does relaxation occur in EC coupling

A

Relaxation occurs following removal of calcium from the cytosol

As cytosolic calcium concentration decreases, it releases from troponin allowing tropomyosin to slide back and block actin’s myosin-binding site leading to release of crossbridges and fibre relaxation

17
Q

What is the sliding filament theory of contraction

A

Overlapping actin and myosin filaments of fixed length slide past each other in an energy-requiring process, resulting in muscle contraction

Myofibrils at resting length have slight overlapping of actin and myosin

During contraction actin and myosin slide past each other

18
Q

How does calcium initiate contraction

A

In resting skeletal muscle, tropomyosin wraps around actin filaments and partially covers actin’s myosin-binding sites (“off” position)

Prior to contraction, tropomyosin must be moved to uncover the remainder of actin’s myosin-binding site (“on”) position

The “off” position of tropomyosin is regulated by troponin

When contraction begins in response to calcium, troponin C binds reversibly to Ca2+

Calcium-troponin C complex pulls tropomyosin away from binding sites (“on”)

Enables myosin heads to bind to actin

19
Q

How does myosin and actin cause contraction

A
  1. ATP binds to myosin and actin is released
  2. ATP hydrolysed to ADP and Pi. Newly formed actin-myosin crossbridge is weak as TM is partially blocking actin’s binding site. Myosin has stored potential energy, like a stretched spring
  3. Ca2+ binds to troponin to uncover rest of the myosin-binding site. Crossbridges become strong as Pi is released. Myosin heads move towards M line, sliding actin with them
  4. ADP released, myosin now back tightly bound to actin in rigor state
20
Q

What is the rigor state

A

No ATP or ADP is bound to myosin – very brief in living muscle

Following death, muscles are unable to bind more ATP so they remain in rigor state

In rigor mortis, the muscles “freeze” due to immovable crossbridges

This lasts for around 24hrs after death until enzymes begin breaking down muscle fibres

21
Q

What is the purpose of creatine kinase

A

enzyme responsible for transfer of the phosphate group from phosphocreatine

22
Q

How is energy tranfered form covalent bonds to ATP

A

Fibres must use metabolism of biomolecules to transfer energy from covalent bonds to ATP
Carbs most efficient and rapid source of ATP

23
Q

How much ATP is produced per Molecule of glucose

A

Aerobic – 30 ATP for each molecule of glucose

Anaerobic – 2 ATP for each molecule of glucose

24
Q

What are the two types of skeltal msucles

A

Type I (MyHC I) – slow-twitch fibres

Type II (MyHC II) – fast-twitch fibres

25
Q

two types of fast twich fibres

A

Type IIa – fast-twitch oxidative glycolytic fibres

Type IIb – fast-twitch glycolytic fibres

26
Q

Why are fast twich fibres quicker

A

Fast-twitch fibres can pump Ca2+ into the sarcoplasmic reticulum faster than slow-twitch fibres, this results in quicker twitches in FT fibres

27
Q

How is ability to resist fatigue related to each fibre

A

Type I / IIa – rely on oxidative phosphorylation for ATP production, so do not fatigue as quick
Type IIb – rely on anaerobic glycolysis for ATP production resulting in quicker fatigue due to H+ accumulation from ATP hydrolysis

28
Q

What does myoglobin do

A
Helps bring oxygen to interior of fibres quickly
Oxidative fibres (I / IIA) contain more so receive oxygen quicker than glycolytic fibres
29
Q

What is isotonic and isometric contractions

A

Isotonic – muscle changes length and creates enough force to move a load
Isometric – muscle does not change length and force created is not enough to move a load