FUNCTIONING OF MUSCLE
In this post we are going to discuss about the Process of Functioning of Muscle. For the post of Muscle System, Click here.
Structure of Contractile Protein :
•Each actin (thin) filament is made of two ‘F’ (filamentous) actins helically wound to each other.
•Each ‘F’ actin is a polymer of monomeric ‘G’ (Globular) actins.
•Two filaments of another protein, tropomyosin also run close to the ‘F’ actins throughout its length.
•A complex protein Troponin is distributed at regular intervals on the tropomyosin.
•In the resting state a subunit of troponin masks the active binding sites for myosin on the actin filaments.
•Each myosin (thick) filament is also a polymerised protein.
•Many monomeric proteins called Meromyosins constitute one thick filament.
•Each meromyosin has two important parts, a globular
head with a short arm and a tail, the former being called the heavy meromyosin (HMM) and the latter, the light meromyosin (LMM). The HMM component, i.e.; the head and short arm projects outwards at regular distance and angle from each other from the surface of a polymerised myosin filament and is known as cross arm.
•The globular head is an active ATPase enzyme and has binding sites for ATP and active sites for actin.
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Mechanism of Muscle Contraction :
•Mechanism of muscle contraction is best explained by the sliding filament theory which states that contraction of a muscle fibre takes place by the
sliding of the thin filaments over the thick filaments.
•Muscle contraction is initiated by a signal sent by the central nervous system (CNS) via a motor neuron.
•A motor neuron alongwith the muscle fibres connected to it constitute a motor unit.
•The junction between a motor neuron and the sarcolemma of the muscle fibre is called the
neuromuscular junction or motor-end plate.
•A neural signal reaching this junction releases a neurotransmitter (Acetyl choline) which generates an action potential in the sarcolemma.
•This spreads through the muscle fibre and causes the release of calcium ions into the sarcoplasm.
•Increase in Ca++ level leads to the binding of calcium with a subunit of troponin on actin filaments and thereby remove the masking of active sites for myosin.
•Utilising the energy from ATP hydrolysis, the myosin head now binds to the exposed active sites on actin to form a cross bridge.
•This pulls the attached actin filaments towards the centre of ‘A’ band.
•The ‘Z’ line attached to these actins are also pulled inwards thereby causing a shortening of the sarcomere, i.e., contraction.
•It is clear from the above steps, that during shortening of the muscle, i.e., contraction, the ‘I’ bands get reduced, whereas the ‘A’ bands retain the length.
•The myosin, releasing the ADP and P1 goes back to its relaxed state.
•A new ATP binds and the cross-bridge is broken.
•The ATP is again hydrolysed by the myosin head and the cycle of cross bridge formation and breakage is repeated causing further sliding.
•The process continues till the Ca++ ions are pumped back to the sarcoplasmic cisternae resulting in the masking of actin filaments.
•This causes the return of ‘Z’ lines back to their original position, i.e., relaxation.
•The reaction time of the fibres
can vary in different muscles.
•Repeated activation of the muscles can lead to the accumulation of lactic acid due to anaerobic breakdown of glycogen in them, causing fatigue.
•Muscle contains a red coloured oxygen storing pigment called myoglobin.
•Myoglobin content is high in some of the muscles which gives a reddish appearance.
•Such muscles are called the
Red fibres.
•These muscles also contain plenty of mitochondria which can utilise the large amount of oxygen stored in them for ATP production.
•These muscles, therefore, can also be called aerobic muscles.
•On the other hand, some of the muscles possess very less quantity of myoglobin and therefore, appear pale or whitish.
•These are the White fibres.
•Number of mitochondria are also few in them, but the amount of sarcoplasmic reticulum is high.
•They depend on anaerobic process for energy.
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