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Effects on the fetal rat intestine of maternal malnutrition and exposure to nitrofen (2,4‐dichlorophenyl‐p‐nitrophenyl ether)

 

作者: Soltanali Mahboob,   Elizabeth R. Hoogenboom,   Robert J. Kavlock,   Frances J. Zeman,  

 

期刊: Teratogenesis, Carcinogenesis, and Mutagenesis  (WILEY Available online 1986)
卷期: Volume 6, issue 1  

页码: 45-57

 

ISSN:0270-3211

 

年代: 1986

 

DOI:10.1002/tcm.1770060106

 

出版商: Wiley Subscription Services, Inc., A Wiley Company

 

关键词: nitrofen;protein‐energy malnutrition;fetal rat intestine;lactase;dipeptidase;morphology

 

数据来源: WILEY

 

摘要:

AbstractThe effects of maternal protein‐energy malnutrition and exposure to nitrofen on selected aspects of intestinal morphology and function were studied in the fetal rat. Pregnant rats were fed, throughout gestation, diets containing 24% or 6% casein as the sole source of protein. Reduced total food intake produced protein‐energy malnutrition (PEM). Each diet group was divided in half and gavaged with either 12.5 mg nitrofen in corn oil/kg/day or corn oil carrier only from days 7 to 21 of gestation. Body weight, intestinal weight, length, and diameter were measured as were villus length (VL), villus width (VW), and number of villi per length of intestine (VMM). Protein (horseradish peroxidase) and lipid absorption were studied histochemically. Lactase and dipeptidase activities were determined in proximal, medial, and distal thirds of the intestine. Results showed that the restricted maternal diet resulted in reduced fetal body weight (BW), intestinal weight (IW) and length (IL), reduced IW/BW and IW/IL ratios, VH, and VMM. The VW was reduced only in the distal third. Protein and lipid absorption were unaffected. Lactase and dipeptidase activities were reduced. Maternal nitrofen exposure resulted in reduced body weight, intestinal size, and lipid absorption, with some evidence of interaction with the diet effects on enzyme activities. It is concluded that effects of maternal malnutrition were extensive, but that nitrofen exposure, at this dosage level, is not likely to contribute to the postnatal fetal mortality rate in either adequately nourished or malnourished r

 

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