The inhibition of lipid peroxidation by Lactobacillus acidophilus and Bifid
obacterium longum was investigated using two lipid model systems. All eight
strains, including six strains oft. acidophilus and two strains of B. long
um, demonstrated an inhibitory effect on linoleic acid peroxidation. The in
hibitory rates on linoleic acid peroxidation ranged from 33 to 46% when 1 m
L of intracellular cell-free extract was tested. In the second model system
, the cell membrane of osteoblast was used as the source for biological lip
id. The results indicated that all strains were able to protect biological
lipids from oxidation. The inhibition rates on cell membrane lipid peroxida
tion ranged from 22 to 37%. The effect of L. acidophilus and B. longum on i
nhibition of fluorescent tissue pigment accumulation was also obtained for
osteoblastic cells. The inhibition rates on fluorescent tissue pigment accu
mulation ranged from 20 to 39%. The antioxidative effect of each milliliter
df intracellular cell-free extract of L. acidophilus and B. longum was equ
ivalent to 104-172 ppm of butylated hydroxytoulene (BHT). These results ind
icated that all strains demonstrated high antioxidative activity. The scave
nging ability of lipid peroxidation products, tert-butyl hydroperoxide and
malondialdehyde, was also evaluated. The results showed that L. acidophilus
and B. longum were not able to scavenge the tert-butyl hydroperoxide. Neve
rtheless, malondialdehyde was scavenged well by these strains.