Acetylcholine Muscarinic Receptors

Muscarinic receptors are widely distributed throughout the body and control distinct functions according to location and subtype (M1 - M5).They are predominantly expressed in the parasympathetic nervous system where they exert both inhibitory and excitatory effects.

Targets
Literature (1)
Receptor Data

Acetylcholine Muscarinic Receptor Target Files

Muscarinic receptor agonists and antagonists could prove useful in the research and treatment of a wide range of central nervous system diseases including Alzheimer's disease and Parkinson's disease.

Literature for Acetylcholine Muscarinic Receptors

Tocris offers the following scientific literature for Acetylcholine Muscarinic Receptors to showcase our products. We invite you to request* your copy today!

*Please note that Tocris will only send literature to established scientific business / institute addresses.


Alzheimer's Disease Poster

Alzheimer's Disease Poster

Alzheimer's disease (AD) is a debilitating and progressive neurodegenerative disease and the most common cause of dementia, affecting approximately 30% of individuals aged over 85 years. This poster summarizes the cellular and molecular mechanisms of AD.

Muscarinic Receptor Pharmacological Data

Receptor Subtype M1 M2 M3 M4 M5
Transduction Mechanism ↑PLC (Gq/11) ↓Adenylyl Cyclase (Gi/o) ↑PLC (Gq/11) ↓Adenylyl Cyclase (Gi/o) ↑PLC (Gq/11)
Primary Distribution Neocortex, hippocampus, neostriatum, salivary glands, eye, heart Brain, heart, smooth muscle, salivary glands Smooth muscle, exocrine glands, brain, autonomic ganglia, salivary glands Neostriatum, cortex, hippocampus, autonomic ganglia Substantia nigra, pars compacta, ventral tegmental area, hippocampus
Tissue Function Learning and memory, neuromodulation, M-current inhibition Bradycardia, smooth muscle contraction, antinociception, hyperthermia, ↓ neurotransmitter release (presynaptic) Smooth muscle contraction, gland secretion, ↓ neurotransmitter release (presynaptic) Regulation of dopamine D1 stimulated locomotor activity Unknown
Key Compounds pKB Values
Agonists Oxotremorine (0843)
Oxotremorine M (1067)
Pilopcarpine (0694)
923*
20286*
4718†
70*
107*
-
881*
8299*
2796†
454*
975*
-
-
-
2476†
Antagonists AF-DX 116 (1105)
AF-DX 384 (1345)
AQ-RA 741 (2292)
4-DAMP (0482)
(S)-(+)-Dimethindene (1425)
J 104129 (2507)
PD 102807 (1671)
Pirenzepine (1071)
J 104129 (2507)
Zamifenacin (2579)
417*
7.5
29*
8.6-9.2
7.08‡
19
5.3
8.5
19*
7.90‡
64-73*
8.2-9.0
3.7*
8.4
7.78‡
490
5.7
6.7
490*
7.93‡
786*
7.8
55*
9.3
6.70‡
4.2
6.2
7.1
4.2*
8.52‡
211*
8.0-8.7
1.5*
8.4-9.4
7.00‡
-
7.3
8.1
-
7.78‡
5130*
6.3
732*
8.9-9.0
-
-
5.2
7.1
-
-

* Ki values, ‡ pKi values, † EC50 value

References

Caulfield and Birdshall (1998) International union of pharmacology. XVII. Classification of muscarinic acetylcholine receptors. Pharmacol.Rev. 50 279. Mansfield et al (2005) Muscarinic receptor subtypes in human bladder detrusor and mucosa, studied by radioligand binding and quantitative competitive RT-PCR: changes in ageing. Br.J.Pharmacol. 144 1089. Pfaff et al (1995) The (S)-(+)-enantiomer of dimethindene: a novel M2-selective muscarinic receptor antagonist. Eur.J.Pharmacol. 286 229. Loudon et al (1997) SB 202026: a novel muscarinic partial agonist with functional selectivity for M1 receptors. J.Pharmacol.Exp.Ther. 283 1059. Burstein et al (1997) Pharmacology of muscarinic receptor subtypes constitutively activated by G proteins. Mol.Pharmacol. 51 312. Mitsuya et al (2000) Discovery of a muscarinic M3 receptor antagonist with high selectivity for M3 over M2 receptors among 2-[(1S,2S)-3-sulfonylaminocyclopentylacetamide derivatives. Bioorg.Med.Chem. 8 825. Watson et al (1995) Characterization of the interaction of zamifenacin at muscarinic receptors in vitro. Eur.J.Pharmacol. 285 135. Mitsuya et al J-104129, a novel muscarinic M3 receptor antagonist with high selectivity for M3 over M2 receptors. Bioorg.Med.Chem.Lett. 7 2555.