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Methacholine



Methacholine
Systematic (IUPAC) name
2-acetyloxypropyl-trimethyl-azanium
Identifiers
CAS number 55-92-5
62-51-1 (chloride)
ATC code  ?
PubChem 1993
Chemical data
Formula C8H18NO2+
Mol. mass 160.234 g/mol
Pharmacokinetic data
Bioavailability  ?
Metabolism  ?
Half life  ?
Excretion  ?
Therapeutic considerations
Pregnancy cat.

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Legal status
Routes  ?

Methacholine chloride is a synthetic choline ester that acts as a non-selective muscarinic receptor agonist in the parasympathetic nervous system. 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 to 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 resistance to acetylcholinesterases.

The primary clinical use of methacholine is to diagnose bronchial hyperreactivity, which occurs in asthma. This is accomplished through the methacholine challenge test. Other therapeutic uses are limited by its adverse cardiovascular effects, such as bradycardia and hypotension, which arise from its function as a cholinomimetic.

Use of methacholine, as well as all other muscarinic receptor agonists, is contraindicated in patients with coronary insufficiency, gastroduodenal ulcers, and incontinence. The parasympathomimetic action of this drug will exacerbate the symptoms of these disorders.


Brand Name

  • Provocholine®

The primary clinical use of methacholine is to diagnose bronchial hyperresponsiveness (due to either hypersensitivity or hyperreactivity).

References

  • Katzung, Bertram G. (2004). Basic and Clinical Pharmacology, 9th. ISBN 0-07-141092-9. 
  • Lötvall J, Inman M, O'Byrne P (May 1998). "Measurement of airway hyperresponsiveness: new considerations". Thorax 53: 419–424. PMID 9708238.
 
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Methacholine". A list of authors is available in Wikipedia.
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