Axon - long slender fibre of a motor neurone. Conducts electrical impulses away from the neutron's cell body to the muscle fibre.
Motor neurons - connected to an axon that connects to skeletal muscle
CNS - consists of the brain and spinal cord. Sends signals called an action potential to a motor unit and travels through a motor neuron
Neuromuscular junction - site where the axon (axon terminal) of the motor neuron and motor end plate of the muscle fibre meet
Sarcoplasm - cytoplasm of a muscle fibre that contains a network of membranous channels surrounding the myofibrils. It is a water solution containing ATP and phosphagens and contains mitochondria
Sarcoplasmic reticulum - the membranous channels that are storage sites for calcium ions. Play important role in muscle contractions.
Myofibrils - muscle fibres are made up of many myofibrils bundled together. Numerous thread-like structures containing contractile proteins
Myosin - a thick, contractile protein filament with protrusions known as 'myosin heads' that bind to form cross bridges.
Sarcomere - basis contractile unit of muscle myofibril distinguish by Z lines. Each sarcomere is composed of 2 main protein filaments: actin and myosin
Actin - a thin contractile protein filament containing 'binding' sites on the two globular proteins: troponin and tropomyosin
Troponin - plays an important role during excitation - contraction, where Ca2+ bind to troponin, then it interacts with tropomyosin to unblock the myosin head binding sites - allows for a cross bridge to start contraction process
Tropomyosin - a 'thread-like' globular protein that blocks myosin head binding sites on actin filament, preventing cross-bridge formation. This prevents contraction in a muscle without nervous innervation and the binding of Ca2+on troponin
Resting phase - no muscle action potential stimulated by the motor neurone so the muscle is at rest
Excitation phase - An impulse travels along the motor neurone to the neuromuscularjunction. If threshold is met, acetylcholine is secreted across the synapse, depolarising the motor end plate, creating a muscle action potential. This muscle action potential causes calcium to be released from the sarcoplasmic reticulum, down the t-tubules into the sarcoplasm
Contraction phase - calcium binds to troponin changing the shape of the tropomyosin to expose the active site on the actin filament. The myosin head attaches to the active site creating a crossbridge. ATP which is attached to the myosin head, is broke down, releasing energy, pulling the actin and myosin filaments towards each other, known as a powerstroke
Recharge phase - The myosin detaches and then reattaches to a new active site further along the actin. ADP detaches from the myosin head and a new ATP molecule attaches and repeats the process, known as the ratchet mechanism.
This continues until no impulse is received or there is depletion of ATP and calcium.
Relaxation phase - The muscle relaxes as it returns to its resting state
All or none law - minimum amount of stimulation is required to start muscle contraction. If an impulse is strong enough then all the muscle fibres in a motor unit will contract. However, is the impulse is less than the threshold then none of the muscle fibres will contract.
Recruitment - number of motor units stimulated. If only a few motor units within the muscle are stimulated, the strength of the contraction will be weak. The greater the number of motor units that are recruited, the greater the number of muscle fibres that will contract. This increases the force that can be produced.
Wave summation - frequency of stimuli. For a motor unit to maintain a contraction, it must receive continuous impulses. Usually a frequency of 80-100 stimuli/sec
Synchronisation - if all motor units stimulated at exactly the same time, maximum force can be applied
Tetanic contraction - occurs after several stimuli cause a muscle to contract in rapid succession
Slow twitch - long distance, endurance activities. Contract slowly over a prolonged period, generating a low level of force and have high levels of resistance to fatigue.
Slow twitch characteristics:
red in colour due to high O2 supply
small fibre size
high mitochondrial density
large capillarisation
high myoglobin content
low PC stores
low glycogen stores
high triglyceride stores
slow speed of contraction
low force of contraction
high resistance to fatigue
Fast twitch - needed in sprint, power and strength activities. Divided into fastoxidativeglycolytic (iia) and glycolytic (iix). They contract quickly over a relatively short period of time generating a high level of force and have low level of resistance to fatigue
Fast twitch characteristics:
large and largest fibre size
low and lowest mitochondrial density
moderate and small capillarisation
moderate and low myoglobin content
high pc stores
high glycogen stores
moderate and low triglyceride stores
fast and fastest speed of contraction
fast and fastest force of contraction
low and lowest resistance to fatigue
Responses from short-term activity:
Increased number of muscle fibres recruited, leading to increased strength of associated muscles
Increased force production, as additional fast twitch muscle fibres are recruited
Increased rate of fibre recruitment - speeds up sports related movements
Type 1 muscle fibres recruited first as they have best threshold
Increased enzyme activity, leading to more efficient breakdown and subsequent re-synthesis of ATP
Adaptations of endurance training:
Results in type iix muscle fibres being converted into type iia
Increased aerobic capacity of slow twitch muscle fibres due to an increase in mitochondrial density and efficiency of aerobic enzymes
Efficiency of the blood supply to the muscles improve slow twitch
Increased storage of fat and glycogen
Slow twitch muscle activation is more effective
Adaptations of power training:
Muscular hypertrophy in fast twitch muscle fibres - greater force produced
Hyperplasia - increased number of type iix fibres
Overall increased muscle fibre recruitment to increase force produced
Increased storage of ATP and PC leads to increased strength and efficiency of type 11a and 11x fibres
Increased neural firing rates, timing and co-ordination of recruitment, increase rate of force production, speed and agility