Thymoquinone, the active constituent of Nigella sativa, was tested in
isolated rat hepatocytes as a hepatoprotective agent against tert-buty
l hydroperoxide (TBHP) toxicity. TBHP (2 mM) was used to produce oxida
tive injury in isolated rat hepatocytes and caused progressive depleti
on of intracellular glutathione (GSH), loss of cell viability as evide
nced by trypan blue uptake and leakage of cytosolic enzymes, alanine t
ransaminase (ALT) and aspartic transaminase (AST). Preincubation of he
patocytes with 1 mM of either thymoquinone or silybin, which is a know
n hepatoprotective agent, resulted in the protection of isolated hepat
ocytes against TBHP induced toxicity evidenced by decreased leakage of
ALT and AST, and by decreased trypan blue uptake in comparison to TBH
P treated hepatocytes. Both thymoquinone and silybin prevented TBHP in
duced depletion of GSH to the same extent. Although thymoquinone prote
cted the liver enzymes leakage, the degree of protection was less than
that caused by silybin. (C) 1998 Elsevier Science Ireland Ltd. All ri
ghts reserved.