EFFECTS OF NICOTINAMIDE ON HEPATOCYTE VIABILITY AND SECRETION OF ALBUMIN AND ALPHA(1)-ACID GLYCOPROTEIN BY ADULT-RAT HEPATOCYTES IN PRIMOCULTURE - COMPARISON WITH DEXAMETHASONE AND RECOMBINANT HUMAN INTERLEUKIN-6
B. Barraud et al., EFFECTS OF NICOTINAMIDE ON HEPATOCYTE VIABILITY AND SECRETION OF ALBUMIN AND ALPHA(1)-ACID GLYCOPROTEIN BY ADULT-RAT HEPATOCYTES IN PRIMOCULTURE - COMPARISON WITH DEXAMETHASONE AND RECOMBINANT HUMAN INTERLEUKIN-6, Biology of the cell, 83(2-3), 1995, pp. 127-133
The effects of nicotinamide on hepatocyte viability and secretion of a
lbumin and alpha(1)-acid glycoprotein were studied in the absence or p
resence of dexamethasone and/or recombinant human interleukin-6 either
after cell attachment (2 h) or after 24, 48, and 72 h of culture. The
evolution of hepatocyte survival during the culture was appreciated b
y measurement of total DNA content. The secretion of albumin and alpha
(1)-acid glycoprotein was measured after a 4-h period following cell a
ttachment or after 24, 48 and 72 h of culture. The important decrease
of DNA content, mRNA levels and secretion of albumin and alpha(1)-acid
glycoprotein in control cultures after 2-3 days was not prevented by
the addition of nicotinamide. In contrast, dexamethasone alone or with
recombinant human interleukin-6 improved DNA content and albumin secr
etion with no additional effect of nicotinamide. The secretion of alph
a(1)-acid glycoprotein was largely induced by dexamethasone alone or d
examethasone and recombinant human interleukin-6. The increase of alph
a(1)-acid glycoprotein secretion was not modified by the addition of n
icotinamide and averaged respectively 27- and 60-fold for dexamethason
e alone and dexamethasone and recombinant human interleukin-6 after 48
h. These observations suggested that nicotinamide, at least in the co
nditions tested here, is unable to prevent alterations of hepatocyte v
iability and gene expression of cultured hepatocytes.