Acetylcysteine

UNDER REVIEW (April 2017)

Mechanism of Action:

NAC is a glutathione precursor that, unlike glutathione, has the potential to cross cell membranes and enter hepatocytes where it restores glutathione (GSH). GSH is necessary for the conversion of the toxic metabolite of paracetamol, NAPQI, to unreactive metabolites. When it is exhausted the toxix metabolites destroy the liver cells. Thus NAC is used to protect the liver from damage in paracetamol overdose. NAC also breaks disulphide bonds that holds mucus glycoproteins together (mucolytic).

Lecture and CAL materials:

  • Lecture: Drugs affecting the respiratory system

 

 

 


Drug specifics

Alternative drug name N-acetylcysteine, NAC, Parvolex®
Effects Prolonged intake of paracetamol may damage liver and kidney. Hepatic toxicity due to metabolite - normally combines with glutathione in liver, but excess metabolite (in overdose) starts binding to nucleophilic constituents (cell proteins) in liver cells, causing cell damage/death. Treatment of poisoning as soon as possible in first 12-48hr by increasing levels of gluathione (give N-acetylcysteine i.v. or methionine orally). see eBNF
Adverse actions Anaphylactoid reaction in 10-15% of patients, usually in the first 30 minutes of administration, due to systemic histamine release.
Dose See ToxBase and eBNF.
Interactions See eBNF.
Contraindications not specified
Comments not specified
Contributors