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Signal transmission from nerve to muscle at the motor end plate. The neuromuscular junction is the synapse that is formed between an alpha motor neuron (α-MN) and the skeletal muscle fiber. In order for a muscle to contract, an action potential is first propagated down a nerve until it reaches the axon terminal of the motor neuron.
When the motor nerve is stimulated there is a delay of only 0.5 to 0.8 msec between the arrival of the nerve impulse in the motor nerve terminals and the first response of the endplate [7] The arrival of the motor nerve action potential at the presynaptic neuron terminal opens voltage-dependent calcium channels, and Ca 2+ ions flow from the ...
As a result, normal functioning can be completely or partially inhibited, with the symptoms largely presenting themselves as problems in mobility and muscle contraction as expected from disorders in motor end plates. Neuromuscular junction diseases can also be referred to as end plate diseases or disorders. [citation needed]
Groups of motor units often work together as a motor pool to coordinate the contractions of a single muscle. The concept was proposed by Charles Scott Sherrington. [2] Usually muscle fibers in a motor unit are of the same fiber type. [3] When a motor unit is activated, all of its fibers contract.
These neurons innervate skeletal muscle fibers through the propagation of action potentials down their axons (through ventral roots and cranial nerves), and they stimulate skeletal muscle fibers at neuromuscular junctions where they synapse with the motor end plates of muscle fibers. In humans, these axons can be as long as one meter.
A neuromuscular non-depolarizing agent is a form of neuromuscular blocker that does not depolarize the motor end plate. [8] The quaternary ammonium muscle relaxants belong to this class. Quaternary ammonium muscle relaxants are quaternary ammonium salts used as drugs for muscle relaxation, most commonly in anesthesia.
[3] [4] In the neuromuscular junction of vertebrates, EPP (end-plate potentials) are mediated by the neurotransmitter acetylcholine, which (along with glutamate) is one of the primary transmitters in the central nervous system of invertebrates. [5] At the same time, GABA is the most common neurotransmitter associated with IPSPs in the brain.
The motor unit consists of a voluntary alpha motoneuron and all of the collective muscle fibers that it controls, known as the effector muscle. The alpha motoneuron communicates with acetylcholine receptors on the motor end plate of the effector muscle. Reception of acetylcholine neurotransmitters on the motor end plate causes contraction of ...