Methacholine

Methacholine
Clinical data
Trade names	Provocholine
AHFS/Drugs.com	Consumer Drug Information
License data	US DailyMed: Methacholine;
Routes of; administration	Respiratory
ATC code	V04CX03 (WHO) ;
Legal status
Legal status	AU: S4 (Prescription only); US: ℞-only;
Identifiers
	IUPAC name 2-(Acetyloxy)-N,N,N-trimethylpropan-1-aminium;
CAS Number	55-92-5 62-51-1 (chloride);
PubChem CID	6114;
DrugBank	DB06709 ;
ChemSpider	5888 ;
UNII	03V657ZD3V;
KEGG	D04970 ;
ChEBI	CHEBI:50142 ;
ChEMBL	ChEMBL978 ;
CompTox Dashboard (EPA)	DTXSID2046967 ;
Chemical and physical data
Formula	C8H18NO2+
Molar mass	160.237 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES [Cl-].O=C(OC(C)C[N+](C)(C)C)C;
	InChI InChI=1S/C8H18NO2.ClH/c1-7(11-8(2)10)6-9(3,4)5;/h7H,6H2,1-5H3;1H/q+1;/p-1 ; Key:JHPHVAVFUYTVCL-UHFFFAOYSA-M ;
	(what is this?) (verify)

Methacholine (INN, USAN) (trade name Provocholine), also known as acetyl-β-methylcholine, is a synthetic choline ester that acts as a non-selective muscarinic receptor agonist in the parasympathetic nervous system.

Medical uses

Methacholine is primarily used to diagnose bronchial hyperreactivity,^[1] which is the hallmark of asthma and also occurs in chronic obstructive pulmonary disease. This is accomplished through the bronchial challenge test, or methacholine challenge, in which a subject inhales aerosolized methacholine, leading to bronchoconstriction. Other therapeutic uses are limited by its adverse cardiovascular effects, such as bradycardia and hypotension, which arise from its function as a cholinomimetic.

Pharmacology

It is highly active at all of the muscarinic receptors, but has little effect on the nicotinic receptors. Methacholine has a charged quaternary amine structure, rendering it insoluble in lipid cell membranes. Clinically, this means that it will not cross the blood–brain barrier and has poor absorption from the gastrointestinal tract. It is broken down at a relatively slow rate within the body, due to its relative resistance to acetylcholinesterases.

The chemical structure of methacholine is derived from acetylcholine by the substitution of a methyl group on the β carbon; this methyl group increases selectivity for muscarinic receptors over nicotinic receptors. The quaternary ammonium group is essential for activity.

Contraindications

Use of methacholine is contraindicated in patients with recent heart attack or stroke, uncontrolled hypertension, known severe airway disease, or aortic aneurysm. It may be used with caution by nursing or pregnant mothers and patients taking certain medications for myasthenia gravis.^[2]

References

^ Birnbaum S, Barreiro TJ (June 2007). "Methacholine challenge testing: identifying its diagnostic role, testing, coding, and reimbursement". Chest. 131 (6): 1932–5. doi:10.1378/chest.06-1385. PMID 17565027.
^ Valentin Popa (2001). "ATS guidelines for methacholine and exercise challenge testing". American Journal of Respiratory and Critical Care Medicine. 163 (1): 292–293. doi:10.1164/ajrccm.163.1.16310b. PMID 11208661.

External links

"Methacholine". Drug Information Portal. U.S. National Library of Medicine. Archived from the original on November 18, 2020.
"Methacholine chloride". Drug Information Portal. U.S. National Library of Medicine. Archived from the original on June 28, 2019.

[pmid17565027-1] Birnbaum S, Barreiro TJ (June 2007). "Methacholine challenge testing: identifying its diagnostic role, testing, coding, and reimbursement". Chest. 131 (6): 1932–5. doi:10.1378/chest.06-1385. PMID 17565027.

[2] Valentin Popa (2001). "ATS guidelines for methacholine and exercise challenge testing". American Journal of Respiratory and Critical Care Medicine. 163 (1): 292–293. doi:10.1164/ajrccm.163.1.16310b. PMID 11208661.

[1]

[2]