The ability of chromium (Cr) salts to increase metallothionein (MT) levels
in rat liver, kidney and pancreas, and its relationship with the presence o
f toxic effects are reported here. Rats were injected subcutaneously with 0
, 10, 20, 30, 40, or 50 mg K2Cr2O7/kg and sacrificed 24 h later. Total Cr a
ccumulation followed a dose-dependent pattern, levels in kidney being highe
r than those in liver or pancreas, suggesting different tissue bioavailabil
ities and accumulation patterns. Cr(IV) administration resulted in a tissue
-specific MT induction: pancreas and liver showed five- and 3.5-fold MT inc
reases, respectively; no increase was observed in the kidney. A positive co
rrelation was observed between zinc and MT concentrations in liver, and bet
ween total Cr and MT concentrations in pancreas. Serum cl-amylase activity
showed a dose-dependent increase starting from 20 mg/kg, whereas serum gluc
ose levels increased at doses higher than 30 mg/kg. Serum aspartate aminotr
ansferase and alanine aminotransferase activities were increased in a dose-
dependent manner, from 20 and 30 mg/kg, respectively. Our results showed th
at treatment with Cr(VI) can induce MT synthesis in pancreas and suggests a
subsequent binding of Cr to MT. Also, pancreas is a target organ for Cr to
xicity, and the usefulness of alpha-amylase activity as a sensitive biomark
er of Cr toxicity in human exposed populations merits further study. (C) 20
00 Elsevier Science Ireland Ltd. All rights reserved.