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. 2006 Jan;61(1):5–15. doi: 10.1111/j.1365-2125.2005.02523.x

Table 3.

NAC in cardiology

Disease Dose of NAC Results
High plasma lipoprotein(a) concentration (1) Orally 2 g day−1 4 weeks→ 4 g day−1 4 weeks (1) Concentration reduction of 70% [83]
(2) Orally 4 g day−1 2 weeks (2) No effect on lipoprotein(a), reduction of homocysteine levels [82]
Unstable angina pectoris, conventional therapy (1) i.v.i. 5 g 6 hourly + i.v.i. NG (1) Fewer infarcts, but severe hypotension [82]
(2) Orally 600 mg three times daily + transdermal NG, 4 months (2) Fewer cardiac events, but intolerable headache [82]
Acute myocardial infarction i.v.i. 15 g per 24 h Decreased level of oxidative stress, more rapid reperfusion, better left ventricular preservation [82]
Acute myocardial infarction i.v.i. 100 mg kg−1 Reduced infarct size, better preservation of global and regional left ventricular function, rudimentary R wave or R wave recovery in left precordial leads [82]
Angina pectoris, normal left ventricular function i.v.i. bolus 2 g, then 5 mg kg−1 h−1 NAC attenuated tolerance development to continuous NG infusion [12]
Chronic heart failure (1) Orally 200 mg kg −1+ i.v.i. NG (1) NG tolerance partly disappeared [82]
(2) i.v.i. 100 mg kg−1 per 30 min + ISDNi (2) Haemodynamic effects of ISDNi potentiated [82]
Viral myocarditis, case report i.v.i. 150 mg kg−1 per 15 min, 6.25 mg kg−1 h−1 Positive inotropic effect [82]
Cardiac catheterization in patients with or without atherosclerosis i.a. 48 mg min−1 Coronary and peripheral endothelium-dependent vasodilation improved [82]

NG, Nitroglycerine; ISDNi, isosorbidedinitrate.