Pregnant rats were treated with a single intravenous or oral administration
of indium chloride (InCl3) on day 9 of pregnancy and their fetuses were ex
amined for growth and malformation on day 20 of pregnancy. By intravenous a
dministration, fetal weight was significantly decreased and the incidences
of fetal mortality and malformation were significantly increased at 0.4 mg
In/kg. Fetal malformations of the tail and digits, e.g., kinked tail, brach
yury, and oligodactyly, were observed at high incidences. By oral administr
ation, similar tendencies in the fetal effects were observed, but there wer
e no significant differences compared to the control even at 300 mg In/kg.
Indium concentrations in the serum of pregnant rats showed low bioavailabil
ity of indium by oral administration. It was concluded from these results t
hat indium showed teratogenicity in rats. Oral treatment with indium may be
developmentally toxic at 300 mg In/kg, but this is difficult to state with
certainty given the limited number of animals that were used in this study
. (C) 1998 Wiley-Liss, Inc.