M. Kanematsu et al., SYNERGISTIC ENHANCEMENT OF NITRITE ON LYSOPHOSPHOLIPID-MEDIATED CYTOLYSIS, Biological & pharmaceutical bulletin, 17(1), 1994, pp. 78-81
Nitrogen oxide, which is produced by activated macrophages, has been d
emonstrated to possess anti-tumor activity. We report herein the syner
gistic effect of sodium nitrite (NO2-) and/or sodium nitroprusside (SN
P) on lysophospholipid (LysoPL)-mediated cytolysis. The incubation of
Cr-51-labeled mouse melanoma (B16) cells with NO2- alone for 3h at 37
degrees C did not induce cytolysis. On the other hand, NO2- significan
tly enhanced the cytolysis of B16 cells in the presence of lysophospha
tidylcholine (LysoPC; 2.0 mu M). A similar effect of NO2- on B16-cytol
ysis was also observed in the presence of 1-O-alkyl-sn-glycero-3-phosp
hocholine (LysoPAF). In addition, SNP (0.05-0.5 mM) synergistically en
hanced B16-cytolysis in the presence of LysoPC. However, nitrate had n
o effect on the cytolysis of B16 cells treated with LysoPC. Furthermor
e, NO2- synergistically enhanced the hemolysis of sheep erythrocytes i
n the presence of LysoPC, but not in the presence of an anti-sheep ery
throcyte antibody and complement. These findings suggest that NO2- dir
ectly affects membrane damage in the presence of LysoPL.