Pentane, a product of lipid peroxidation, has been detected in situati
ons involving ischemic injury. Such injury may be limited if lipid per
oxidation can be controlled by antioxidants. The role of lipid peroxid
ation in chronic heart failure (CHF) was assessed by measuring breath
pentane in patients with CHF vs. age matched controls. The effect of a
free radical scavenger on pentane released during CHF was also measur
ed. Pentane levels were correlated with the daily dose of captopril, a
sulfhydril-containing drug used to treat CHF, which is an angiotensin
converting enzyme inhibitor. To separate the scavenging effects of ca
ptopril from the pharmacologic effects of converting enzyme inhibitors
, a crossover study using a nonsulfhydril inhibitor was used. Patients
with CHF excreted (p < 0.005) high concentrations of pentane (5.7 +/-
2.1 vs. control 3.6 +/- 1.2 nmol/l). Patients treated with captopril
also had significantly higher (p < 0.05) excretion of pentane than the
control patients (4.7 +/- 1.3 vs. 3.6 +/- 1.2 nmol/l). The dose of ca
ptopril was inversely proportional to the concentration of pentane exc
reted (r = 0.55, p < 0.05). Pentane excretion during captopril therapy
was significantly lower before (p < 0.01) and after (p < 0.02) nonsul
fhydril inhibitor therapy. Conclusion: breath pentane is elevated in C
HF and it can be reduced by a free radical scavenger. This reduction o
f pentane excretion is not a converting enzyme inhibitor class effect.