Excitation Contraction Coupling Flashcards
How is the neuronal action potential propagated to the muscle? Describe what is happening in the neuron.
The AP propagates down the neuron to the presynaptic terminal (terminal button) where it depolarizes it and causes voltage-gated Ca channels to open. Increase in Ca causes vesicles to fuse with the membrane and release ACh into the synaptic cleft.
How is the neuronal action potential propagated to the muscle? Describe what is happening in the synaptic cleft and the muscle.
ACh binds to ACh receptors embedded in the muscle plasma membrane at the motor endplate. ACh receptors open and allow Na to flow in (a little K out) changing the endplate potential. Voltage-gated Na channels are then activated and the AP propagates down the muscle.
What is Myasthenia Gravis? Explain it.
It is an autoimmune disease where antibodies block or reduce the number of nicotinic acetylcholine receptors at the neuromuscular junction resulting in muscle fatigability.
How is Myasthenia Gravis treated? What clinical presentation does it have?
Treated with edrophonium chloride which is a cholinesterase inhibitor and thus increases ACh at the neuromuscular junction. Patients will have ptosis and weakness of smile. They may feel fine in the morning but develop diplopia and speech slur later in the day. They can not resist a physician pushing their head to pull their chin off of their chest.
Disorders of excitation contraction coupling include the following: 1-Amyotrophic lateral sclerosis. 2-Demyelinating disease (eg. Guillain-Barre Syndrome). 3-Myasthenia Gravis. 4-Malignant hyperthermia. 5-Muscular dystrophy. Explain with which part each interferes.
1- Motor Neuron Disease 2- Nerve disease 3- Neuromuscular Junction Disease 4- Sarcomere disease 5- Muscle disease (pg 252)
Can skeletal muscle contract in the absence of extracellular calcium?
Yes, the cycling of calcium is intracellular. The Na dependent AP triggered by ACh release at the neuromuscular junction triggers the release of Ca from an internal store inside the muscle cell.
Describe the skeletal muscle AP and Ca release
The sarcolemma and T-tubules are depolarized in a Na dependent mechanisms. The depolarization of T-tubules induces a change in the structure of L-type Ca channels (embedded in the T-tubule) which in turn opens a Ca channel gate in the ryanodine receptors embedded in the sarcoplasmic reticulum releasing Ca into the sarcoplasm (cytosol)
What composes the skeletal muscle triad?
1 T-tubule and 2 sarcoplasmic reticulum cisternae
How are the terminal cisternae of SR physically attached to the T-tubules?
Through the direct coupling of L-type Ca channels embedded in the T-tubule membrane to the Ryanodine receptors embedded in the membrane of the SR.
At nonmolar concentrations and micromolar concentrations what effect does the plant alkaloid Ryanodine have?
Nanomolar - opens
Micromolar - closes
In which type of muscle is Ca induced Ca release most important? Describe the process
Cardiac muscle. The Ryanodine receptor is stimulated to open by the presence of cytoplasmic Ca. So after the L-type Ca channels open the ryanodine receptors at the triad Ca is released and causes more ryanodine receptors to release Ca. Ultimately, Ca release occurs rapidly along the entire length of the SR and not just at the triad.
How is skeletal muscle contraction terminated?
By the removal of calcium from the sarcoplasm
What is the major mechanism for Ca removal from the sarcoplasm in skeletal muscle?
The Sarcoplasmic Reticulum Ca ATPase (SERCA). It uses ATP hydrolysis to pump Ca into the SR where it is bound by Ca binding proteins Calreticulin and Calsequestrin. Ca is retained in the cell.
What are the two mechanisms of Ca removal from the sarcoplasm that extrude Ca into the extracellular fluid?
The plasma membrane Ca ATPase (PMCA). It pumps 1 Ca out per ATP used. The second is the Sodium Caclium exchanged (NCX). It lets 3 Na ions into the cell to remove 1 Ca from the cell.
An increase in muscle tension from successive action potentials is called?
Summation