We have investigated the inhibition of lipid peroxidation by beta-carboline
derivatives, synthesized by Pictet-Spengler condensation of tryptophan wit
h formaldehyde, acetaldehyde, pyruvic acid and pyridoxal HCl, in rat brain
homogenate and liver mitochondria and microsomes. The antioxidant activity
of the compounds was also evaluated by the linoleic acid autoxidation syste
m. Out of the four compounds tested, one (tetrahydro beta-carboline) optima
lly inhibited spontaneous and iron-induced lipid peroxidation in brain homo
genate. It also inhibited lipid peroxidation induced by ferrous-ascorbate i
n liver mitochondria, as well as ferrous-ADP-ascorbate and NADPH-induced li
pid peroxidation in liver microsomes. In addition, this compound exhibited
antioxidant activity in the linoleic acid autoxidation system and its antio
xidant activity was comparable to that of the standard antioxidant viz buty
lated hydroxy anisole. Its higher antioxidant activity may be attributable
to its structure. Med Sci Res 27:181-184 (C) 1999 Lippincott Williams & Wil
kins.