The present study aimed to examine the effect of astilbin, a flavanoid, on
liver injury. When administered during the effector but not induction phase
, astilbin significantly decreased the liver injury induced by delayed-type
hypersensitivity to picryl chloride in mice. The pretreatment of nonparenc
hymal cells but not hepatocytes with astilbin in vitro caused a concentrati
on- and time-dependent inhibition against the damage. Nonparenchymal cells
isolated from astilbin-administered mice also showed a significant incompet
ence of hepatotoxicity, correlated with the inhibition of serum transaminas
e elevation. However, astilbin did not protect from CCl4-induced liver dama
ge. Furthermore, the flavanoid markedly promoted the apoptosis of nonparenc
hymal cells from liver-injured mice, whereas did not influence those from n
aive mice. These results suggest that astilbin provides improvement against
liver injury through a selective dysfunction of liver-infiltrating cells r
ather than by protecting the hepatocyte membrane. Such characteristics will
be of significance to pave a new way for treating immunologically related
liver diseases and for developing new drugs. (C) 1999 Elsevier Science B.V.
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