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

Citation
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
Citations number
34
Categorie Soggetti
Cell Biology
Journal title
ISSN journal
02484900
Volume
83
Issue
2-3
Year of publication
1995
Pages
127 - 133
Database
ISI
SICI code
0248-4900(1995)83:2-3<127:EONOHV>2.0.ZU;2-V
Abstract
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.