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Methacholine

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Chemical compound
Pharmaceutical compound
Methacholine
Clinical data
Trade names Provocholine
AHFS/Drugs.com Consumer Drug Information
License data
Routes of
administration
Respiratory
ATC code
Legal status
Legal status
Identifiers
  • 2-(Acetyloxy)-N,N,N-trimethylpropan-1-aminium
CAS Number
PubChem CID
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
Formula C8H18NO2+
Molar mass 160.237 g·mol−1
3D model (JSmol)
  • [Cl-].O=C(OC(C)C[N+](C)(C)C)C
  • InChI=1S/C8H18NO2.ClH/c1-7(11-8(2)10)6-9(3,4)5;/h7H,6H2,1-5H3;1H/q+1;/p-1 checkY
  • Key:JHPHVAVFUYTVCL-UHFFFAOYSA-M checkY
 NcheckY (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

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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

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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

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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

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  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.
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mAChRs Tooltip Muscarinic acetylcholine receptors
Agonists
Antagonists
Precursors
(and prodrugs)

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