Target intelligence / Profile preview

Nicotinic Acetylcholine Receptor (Skeletal Muscle Type) (nAChR (Skeletal Muscle))

Target
nAChR (Skeletal Muscle)
Molecular classification
Ligand-gated ion channel, Receptor
01

Overview

The nicotinic acetylcholine receptor (nAChR), specifically the skeletal muscle type, is a ligand-gated ion channel located at the postsynaptic membrane of neuromuscular junctions in skeletal muscle. It is essential for converting chemical signals from motor neurons into electrical signals that trigger muscle contraction. The muscle-type nAChR is a heteropentamer composed of five subunits (two α1, one β1, one δ, and either one γ (fetal) or one ε (adult) subunit). When acetylcholine binds, it induces a conformational change that opens the central pore, allowing Na⁺ influx and K⁺ efflux, leading to muscle contraction. It is the target of drugs like curare derivatives, which are used as paralytics. Dysfunction is associated with myasthenia gravis.

Other names
Muscle-type Nicotinic Acetylcholine ReceptorSkeletal Muscle nAChRAChR (Muscle)
02

Mechanism of action

Agonist binding opens the ion channel, allowing Na+ influx and K+ efflux, leading to depolarization and muscle contraction. Antagonists block the channel, preventing ion flow and muscle contraction.

03

Biological functions

Neuromuscular transmissionSynaptic signalingIon channel activity
04

Disease associations

Myasthenia Gravis
05

Safety considerations

Paralysis
06

Interacting drugs

Acetylcholine

2 more in the full profile.

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