ACH receptors can be defined as an integral membrane protein that responds to the binding of acetylcholine, a neuoyansmitter. Two example are nicotinic acetyl line receptors and muscarinic acetylcholine receptors. .
An acetylcholine receptor is a feature of neurons which detects the presence of acetylcholine as part of neural activity.
Nicotinic receptors are closed until ACh molecules bind to the receptor proteins.
Acetylcholine or aka ACH is the neurotransmitter that is released from the axon terminal to through the neuromuscular junction across the synaptic cleft which binds to the ACH receptors on the end motor plate of the Sarcolema.
When the Ach binds to receptor sites on the muscle cell membrane it causes channels to open and allows Na+ to move into the cell which then causes an action potential.
It can act presynaptically on Nicotinic 2 receptors which increases the release of AcH potentiating the block at the motor end plate.
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Nicotinic receptors are closed until ACh molecules bind to the receptor proteins.
ACh (acetylcholine) binds to receptors at the NMJ (neuromuscular junction) to induce contraction of muscle.
AChE destroys the ACh and they are removed from the membrane receptors.
ACh esterase, which breaks ACh down into an acetyl group and a choline group. This is then taken up by the neurone and some is reformed into ACh.
Neostigmine is a competitive irreversible inhibitor of Acetylcholinesterase (AChE), an enzyme responsible for breaking down acetylcholine (ACh). Myasthenia gravis is caused by the body producing too little ACh receptors. As stimulating the ACh receptors is needed for nervous transmission, the nerve signals cannot be transmitted causing muscle weakness and fatigue. Neostigmine is hence used to inhibit AChE so that less ACh gets broken down. This leads to more ACh binding to the ACh receptors causing muscular contraction.
they stimulate the action of ACh at post ganglionic muscarinic receptors.
Competes with ACh at the nerve receptors and results in under stimulatin of the receptors.
Competes with ACh at the nerve receptors and results in under stimulatin of the receptors
It doesn't atropine only acts on muscarinic receptors (it's a competitive antagonist here for ACh), but histamine acts on different receptors (histamine receptors). There is no direct interaction between atropine and histamine receptors
myasthenia gravis
At autonomic ganglia and after post ganlionic parasympathetic fibres. With few exceptions
Preganglionic fibers for the SNS release ACh; so a drug that stimulates ACh receptors would stimulate the postganglionic fibers of sypathetic nerves, resulting in increased sympathetic activity