3.6.3 Skeletal Muscles

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19 Terms

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antagonistic pairs

muscles can only pull so they work in pairs to move bones around joints - pull in opposite directions

-agonist contracts while antagonist relaxes

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gross structure of skeletal muscle

myofibrils = muscle cells fused together to form bundles of parallel muscle fibres

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microscopic structure of skeletal muscle

-myofibrils divided into sarcomeres

-sarcoplasm = muscle cell’s cytoplasm with lots of mitochondria + glycogen granules and sarcoplasmic reticulum

-sarcolemma = cell membrane which folds inwards and sticks into sarcoplasm to form T-tubules (transverse)

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roles of different features

-mitochondria + glycogen granules = provide ATP + hydrolysed into glucose for respiration

-sarcoplasmic reticulum = stores and releases Ca2+ ions 

-T-tubules = help to spread electrical impulses to sarcoplasmic reticulum

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myofibrils structure

-myosin = thick filament
-actin = thin filament

-Z-line = boundary between sarcomeres

-M-line = middle of filaments

-I-band = only actin = light

-A-band = overlap of actin + myosin = dark

-H-zone = only myosin

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sliding filament theory 

-myosin + actin filaments slide over one another to make sarcomeres contract so myofibrils + muscles contract

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evidence that supports theory

-H-zone narrows

-I-band narrows

-Z-lines get closer

-A-band remains the same

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STAGES of muscle contraction 1) stimulation of muscle

same process as synapse but at neuromuscular junction instead always with acetylcholine from motor neurone to skeletal muscle cell

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STAGES of muscle contraction 2) arrival of action potential

-sarcolemma is depolarised + action potential travels down T-tubules to sarcoplasmic reticulum

-causes voltage-gated Ca2+ channels to open in reticulum so releases Ca2+ ions into sarcoplasm

-Ca2+ ions bind to troponin attached to tropomyosin causing conformational change of troponin

-so tropomyosin is removed and myosin binding sites are exposed

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STAGES of muscle contraction 3) binding of myosin head

-myosin head in low energy configuration so ATP binds to myosin head + is then hydrolysed causing head to bend into high energy configuration

-myosin pulled back into position and binds to actin binding site to form actin-myosin cross bridge

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STAGES of muscle contraction 4) movement of actin filament

-Ca2+ ions also activate enzyme ATP hydrolase which hydrolyses ATP into ADP + Pi for energy

-power stroke = causes head to move and pull actin filament over myosin

-actin moves towards centre of sarcomere

-head is now in low energy configuration

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STAGES of muscle contraction 4) breaking of cross bridge

ADP + Pi dissociate but another ATP molecule binds to myosin head and breaks cross bridge

-myosin head detaches from actin + returns to original position

-myosin reattaches to different binding site further along

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STAGES of muscle contraction 5) muscle relaxing

-Ca2+ ions leave binding sites and are actively transported back into sarcoplasmic reticulum through Ca2+ ATPase pump

-tropomyosin moves back and blocks actin-myosin binding sites

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energy for muscle contraction

1) aerobic respiration - generates ATP, for long periods of low exercise

2) anaerobic respiration - makes ATP rapidly by glycolysis, for short periods of hard exercise

3) ATP-phosphocreatine system 

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phosphocreatine (PCr)

-PCr reacts with ADP and adds a phosphate group to produce ATP + creatine

-PCr is stored inside cells and generates ATP very quickly, for short bursts of vigorous exercise

-anaerobic respiration

-some creatine get broken down into creatinine which is removed via kidneys

ADP + PCr → ATP + Cr

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slow twitch muscle fibres

-found in sites of sustained contraction/posture e.g. calves

-long duration contraction - work for long time

-energy is released slowly through aerobic respiration to prevent lactate buildup

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PROPERTIES of slow twitch muscle fibres

-glycogen = many ends can be hydrolysed to release glucose for respiration

-contain myoglobin = higher affinity for oxygen at lower partial pressures, reddish colour

-many mitochondria + blood vessels = high supply of ATP + oxygen

-mitochondria found near edge = short diffusion pathway for oxygen

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fast twitch muscle fibres

-found in sites of rapid, powerful contraction/fast movement

-short-term contraction - get tired quickly

-energy is released quickly through anaerobic respiration using glycogen

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PROPERTIES of fast twitch muscle fibres

-large store of PCr = energy can be generated very quickly

-more + thicker myosin filaments

-few mitochondria + blood vessels = get fatigued easily

-less myoglobin = pale colour