0429 Excitation-contraction coupling in muscle Flashcards
• Describe the sequence of events involved in skeletal muscle contraction starting from synaptic transmission at the neuromuscular junction to the shortening of the sarcomere • Outline the key proteins involved in contraction and the significance of the cross‐bridge cycle • Recognise the role of Ca2+ in muscle contraction • Describe the mechanisms by which Ca2+ enters and exits skeletal and cardiac muscle cells, and how smooth muscle may differ • Compare / contrast the structural and fu
Briefly describe the synaptic transimission from axon hillock of a motor neuron to the nerve terminal (use ACh as a NT)
Motor neuron fires, causing influx of Ca2+ via depolarisation at the nerve terminal. This signals vesicle fusion with the pre-synaptic membrane, releasing ACh in vesicles into synaptic cleft. ACh binds to nicotinic receptors on the post-synaptic membrane, opening Na+/K+ channels and causing EPSP. ACh is degraded in the synaptic cleft by AChE and choline is transported back into terminal
What is excitation-contraction coupling
It is the excitation of a muscle membrane (due to NMJ synaptic transmission) that leads contraction of muscles
What determines the innervation ratio of a motor neuron in muscle
The function of the neuron. E.g. a fine movement generally involves 3 fibres/neuron. A strong, course movemnt canuse 100 to 1000 fibres/neuron
What is the role of the Sarcolemma, T tubule and Sarcoplasmic reticulum in excitation-contraction coupling
Sarcolemma = plasma membrane of the cell down with AP propagates. The T tubules allow AP propagation to distribute throughout the myofibrils. SR contains the Ca2+ ions that a released into the sarcoplasm and initiate the cross bridge cycling
What is the triad? What receptors are found on it and what are their roles
A triad = terminal cisternae + T tubule + terminal cisternae (part of SR). Dihyropyridine channels (DHP) are found on the T tubules. They are coupled to Ryanodine receptors on the SR. Activation of DHP (due to AP) stimulates ryanodine receptrs which release Ca2+ stored in SR into the sarcoplasm to initiate cross bridge cycle
What are the main players in relaxation of the muscle (i.e. removal of intracellular Ca2+
SERCA (sarco/endoplasmic reticulum calcium ATPase). Calsequrestrin and sarcalumenin
Describe the structure of skeletal muscle (fasicle is made of …., made of…..) down to the thick and thin filaments
Fasicle is made of muscle bundles. Muscle bundle is made of muscle fibres. Muscle fibres are myofibrils. Myofibrils are made of thick and thin filaments
Describe the Z lines, I,A and H bands
Z line demarcate one sarcomere (distance between 2 Z lines). I band contains actin (thin) filaments and no myosin. A band marks the length of myosin filaments. H band contains myosin (thick) filaments, no actin.
During contraction which bands shorten and which bands remain the same length
The A band (length of thick, myosin filaments) stays the same. The H and I bands (myosin and actin only sections) shorten.
Describe the structure of the thin, actin filaments (include actin, troponin, tropomyosin) and their component functions
Actin filaments back the backbone of the filament. Troponin/troponin complex (T,I,C) controls the position of tropomyosin. Tropomyosin wraps around the actin and blocks the myosin binding sites
Where do calcium ions from the sarcoplasm bind to on the thin filaments
The troponin complex (specifically troponin C)
Describe the structure of the thick filaments (tail and cross bridge region) and their component functions
Myosin consists of a tail region (structure of thick filament) and the cross-bridge region. CB region contains the neck and globular heads which binds to actin and makes a cross bridge
Briefly describe the cross bridge cycle (after calcium has bound to troponin, exposing the myosin binding site on actin)
Resting myosin heads contain ATP. Exposure of binding site means myosin and actin join to form a cross bridge. Once bound, myosin heads release phosphate (ATP to ADP) and pull the actin filament towards centre of sarcomere. Myosin release ADP (remains attached). Finally ATP binds to myosin which releases it from actin. Repeat cycle
What would happen if there is no ATP available in muscle
Then the actin and myosin filaments would be stuck in attachment state (contraction but no relaxation of muscle). An example of this is rigor mortis
What are the differences between fast and slow twitch skeletal muscles in terms of contraction (think cross bridges and Ca2+ elimination)
Fast twitch (type 2) muscle fibres have faster cross bride cycles and SERCA 1. Slow tiwtch (type 1) fibres have slower cross bridge cycles and SERCA 2