Fumonisin B-1 (FB1), the major mycotoxin from Fusarium moniliforme, ha
s been implicated as a causative agent in several animal and human dis
eases. Despite animal toxicity studies and human epidemiological studi
es of FB1, knowledge of its reproductive effects is scarce. In this st
udy, one of a series of proposed studies that will allow extrapolation
to humans, pregnant rats were given oral doses of 0, 1.875, 3.75, 7.5
or 15 mg FB1/kg on gestation days 3-16. Caesarean sections were perfo
rmed on day 17 or 20, and maternal condition, implantation efficiency,
foeta1 viability and foetal development were measured. Dose-related d
ecreases in overall feed consumption and body weight gain were seen, b
ut only the feed consumption decrease at 15 mg/kg, and the decreased b
ody weight gain at 15 mg/kg on days 0-17 were statistically significan
t. Foetal body weights at day 17 were similar in control and treated g
roups; but in day-20 foetuses, female weight and crown-rump length wer
e significantly decreased at 15 mg/kg. FBI was not teratogenic at the
doses tested, and no dose-related effects were seen in either skeletal
or soft-tissue development. In day-I7 animals, maternal and foetal br
ain, liver and kidney tissues, and maternal serum were preserved to st
udy the levels of sphinganine (Sa), sphingosine (So), and the Sa/So ra
tios. Dose-related increases were seen in Sa/So ratios in maternal liv
ers, kidneys and serum. Sa/So ratios of maternal brains were not affec
ted, nor were those of foetal kidneys, livers or brains. Published by
Elsevier Science Ltd.