Isolated hepatocyte suspensions prepared by collagenase perfusion released
high levels of nitrite into the extracellular medium during an 8-hr incubat
ion. The release was time dependent, with increases first occurring by 4 hr
and continuing throughout the remainder of the incubation period. Nitrite
production was inhibited by the nitric oxide synthase (NOS) inhibitors amin
oguanidine and N-G-nitro-L-arginine methyl ester (L-NAME), indicating that
the nitrite is derived from nitric oxide (NO) production from NOS activity.
Nitrite production was not related to bacterial or Kupffer cell contaminat
ion. The protein synthesis inhibitor cycloheximide and the transcription in
hibitor actinomycin D also prevented nitrite production by parenchymal hepa
tocytes. Calcium-independent NOS enzyme activity increased with incubation
times, and this increase coincided with the observed increases in nitrite p
roduction. Our results suggest that NOS is induced following the isolation
of hepatocytes, and this induction results in the formation of high levels
of NO. BIOCHEM PHARMACOL 57;11:1223-1226, 1999. (C) 1999 Elsevier Science I
nc.