3-Chloro-4-(dichloromethyl)-5-hydroxy-2(5H)-furanone (MX) as a Direct-Acting Teratogen in Micromass in vitro Tests |
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Authors: | Shoji TERAMOTO Ken L. TAKAHASHI Masayuki KIKUTA Hiroko KOBAYASHI |
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Affiliation: | Toxicology Division, Institute of Environmental Toxicology, Uchimoriya-cho 4321, Mitsukaido, Ibaraki 303–0043, Japan;Chemistry Division, Institute of Environmental Toxicology, Uchimoriya-cho 4321, Mitsukaido, Ibaraki 303–0043, Japan |
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Abstract: | 3-Chloro-4-(dichloromethyl)-5-hydroxy-2( 5H )-furanone (MX) causes complete inhibition of rat embryonic midbrain (CNS) cell differentiation in the micromass in vitro test when applied at a concentration of 5 μ g/ml under conditions where MX is rapidly degraded in culture medium with a half-life of 56 min. This study investigated whether or not degradation products of MX have inhibitory effects on CNS cell differentiation following pre-incubation of MX in culture medium for 0.5, 1 or 2 hr. When MX was pre-incubated for 0.5 hr, the mean number of differentiated foci was 0.2 against 62.5 for the control. However, the number increased to 44.7 when pre-incubation time was extended to 2 hr. These results suggest that MX, but not its degradation products, is a teratogen in vitro. MX manifested almost complete inhibitory effects on CNS cell differentiation by 0.5 hr of exposure. |
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Keywords: | MX direct-acting teratogen micromass test chlorination by-product |
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