## Abstract Pregnant Wistar rats were given butyl benzyl phthalate (BBP) at a dose of 2.0% in the diet on days 0β20, days 0β11 or days 11β20 of pregnancy. Food consumption and body weight gain were decreased in pregnant rats given BBP. Preβimplantation loss in the BBPβtreated groups was comparable
Evaluation of the teratogenic potential of the plasticizer butyl benzyl phthalate in rats
β Scribed by Makoto Ema; Toshimi Murai; Takafumi Itami; Hironoshin Kawasaki
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 485 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0260-437X
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β¦ Synopsis
The teratogenicity of butyl benzyl phthalate (BBP) was studied in Wistar rats. Pregnant rats were given BBP at a dosage of 0, 0.25, 0.5, 1.0 or 2.0% in the diet from day 0 to day 20 of pregnancy. Daily intakes of BBP were 185 mg kg-' for the 0.25% group, 375 mg kg-' for the 0.5% group, 654 mg kg-' for the 1.0% group and 974 mg kg-' for the 2.0% group. Adjusted maternal body weight gain (body weight gain excluding the gravid uterus) during pregnancy in the 1.0 and 2.0% groups was significantly lowered. Food consumption during pregnancy in the 0.25 and 0.5% groups did not differ from that in the control group. No death was noted in the pregnant females of any group. There was no significant compound-related effects on the incidence of preimplantation loss. All dams given 2.0% BBP exhibited complete resorption of all the implanted embryos. Morphological examinations of the fetuses revealed no evidence of teratogenesis. It could be concluded that the no-observable-effect-levels (NOEL) in rats were 0.5 and 1.0% BBP in the diet for maternal and embryofetal toxicity, respectively.
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The objective of this study was to determine the susceptible day for the developmental toxicity of butyl benzyl phthalate (BBP) by a single administration on one of the days during organogenesis. Pregnant rats were given a single dose of BBP by gastric intubation at a dose of 1000 mg kg(-1) on one o
The embryolethality of butyl benzyl phthalate (BBP) was studied in Wistar rats. Pregnant rats were given BBP at dosages of 0 (control) and 2.0% in the diet from day 0 to day 20 of pregnancy. Daily intake of BBP was 974 mg kg-1 for the 2.0% BBP group. In this group, all dams exhibited complete resorp
The teratogenic potential of dibenzthiazyl disulphide (MBTS) was studied in Wistar rats. Pregnant rats were given MBTS at a dosage of 0, 0.04, 0.2 or 1 % in the diet from day 0 to day 20 of pregnancy. Daily intakes of MBTS were 26 mg kg-' for the 0.04% group, 127 mg kg-' for the 0.2% group and 596 m
The objective of the present study was to determine if periods of exposure would modify the developmental toxicity of butyl benzyl phthalate (BBP). Pregnant Wistar rats were given BBP at a dose of 2.0% in the diet on days 0-20, days 0-7, days 7-16 or days 16-20 of pregnancy. Food consumption and bod