Muscarinic agonist
Template:Short description Template:Infobox drug class
A muscarinic acetylcholine receptor agonist, also simply known as a muscarinic agonist or as a muscarinic agent, is an agent that activates the activity of the muscarinic acetylcholine receptor.[1] The muscarinic receptor has different subtypes, labelled M1-M5, allowing for further differentiation.
Clinical significance
M1
M1-type muscarinic acetylcholine receptors play a role in cognitive processing. In Alzheimer disease (AD), amyloid formation may decrease the ability of these receptors to transmit signals, leading to decreased cholinergic activity. As these receptors themselves appear relatively unchanged in the disease process, they have become a potential therapeutic target when trying to improve cognitive function in patients with AD.[2][3][4]
A number of muscarinic agonists have been developed and are under investigation to treat AD. These agents show promise as they are neurotrophic, decrease amyloid depositions, and improve damage due to oxidative stress. Tau-phosphorylation is decreased and cholinergic function enhanced. Notably several agents of the AF series of muscarinic agonists have become the focus of such research:. AF102B, AF150(S), AF267B. In animal models that are mimicking the damage of AD, these agents appear promising.
The dual M1, M4 agonist xanomeline has been proposed as a potential treatment for schizophrenia.[5][6] Xanomeline/trospium chloride was approved in the US in 2024.[7] Based on preclinical pharmacological and genetic studies, M1 predominantly modulates cognitive symptom domains and modestly regulates psychosis symptom domains.[8]
M3
In the form of pilocarpine, muscarinic receptor agonists have been used medically for a short time.
- M3 agonists
- Aceclidine, for glaucoma
- Arecoline, an alkaloid present in the Betel nut
- Pilocarpine is a drug that acts as a muscarinic receptor agonist that is used to treat glaucoma
- Cevimeline (AF102B) (Evoxac®) is a muscarinic agonist that is a Food and Drug Administration (FDA)-approved drug and used for the management of dry mouth in Sjögren's syndrome
M4
Xanomeline exerts its action partially through the M4 receptor. Based on preclinical pharmacological and genetic studies, M4 receptors appear to modulate both psychosis and cognitive symptom domains.[9][8]
Muscarinic versus nicotinic activity
| Comparison of cholinergic agonists [10] | ||||
|---|---|---|---|---|
| Substance | Receptor specificity | Hydrolysis by acetylcholinesterase | Comments | |
| Muscarinic | Nicotinic | |||
| Acetylcholine | +++ | +++ | +++ | Endogenous ligand |
| Carbachol | ++ | +++ | - | Used in the treatment of glaucoma |
| Methacholine | +++ | + | ++ | Used to diagnose bronchial hyperreactivity,[11] a hallmark of asthma and COPD. |
| Bethanechol | +++ | - | - | Used in bladder and gastrointestinal hypotonia. |
| Muscarine | +++ | - | - | Natural alkaloid found in certain mushrooms.
Cause of one form of mushroom poisoning |
| Nicotine | - | +++ | - | Natural alkaloid found in the tobacco plant. |
| Pilocarpine | ++ | - | - | Used in glaucoma. |
| Oxotremorine | ++ | +[12] | - | Used in research to induce
symptoms of Parkinson's disease. |
Muscarinic acetylcholine receptor subtypes
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See also
- Muscarine
- Muscarinic acetylcholine receptor
- Muscarinic antagonist
- Nicotinic acetylcholine receptor
- Nicotinic agonist
- Nicotinic antagonist
References
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External links
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