Developmental Toxicity of Fungicide Carbendazim in Female Mice

被引:59
作者
Farag, Amina [1 ]
Ebrahim, Hala [1 ]
ElMazoudy, Reda
Kadous, Ezzat [1 ]
机构
[1] Univ Alexandria, Dept Pesticide, Fac Agr, Fac Sci,Dept Zool, Alexandria 55555, Egypt
关键词
embryogenesis; environmental issues; maternal-fetal interactions; pesticides; METHYL 2-BENZIMIDAZOLE CARBAMATE; BENZIMIDAZOLE CARBAMATE; SERUM TRIGLYCERIDES; RAT TESTIS; IN-VIVO; BENOMYL; OSSIFICATION; INHIBITION; METABOLISM; BINDING;
D O I
10.1002/bdrb.20290
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This study investigated the developmental toxicity of carbendazim during the organogenesis period in mice. Mated CD-1 mice were administered carbendazim at dose levels 0, 150, 300, and 600 mg/kg/day by gavage. Body weights, weight gains, and feed consumption were significantly reduced in mice administered with 300 and 600 mg/kg/day. Carbendazim exposure increased maternal levels of cholesterol, triglyceride, glucose, protein, and creatinine; and reduced the levels of estradiol and progesterone in the 300- and 600-mg/kg/day groups. In addition, exposure to carbendazim significantly reduced the number of live fetuses and increased the number of dead and resorptions at the same dose levels. External, visceral, and skeleton malformations were observed in the 300- and 600-mg/kg/day. In conclusion, exposure of pregnant mice to carbendazim induced maternal and developmental toxicity at 300 and 600 mg/kg/day. 150 mg/kg/day carbendazim produced a very slight increase in postimplantation loss, which was within the range of historical controls, and no evidence of maternal toxicity. Birth Defects Res (Part B) 92:122-130, 2011. (C) 2011 Wiley-Liss, Inc.
引用
收藏
页码:122 / 130
页数:9
相关论文
共 58 条
[1]  
Akbarsha M A, 2001, Indian J Exp Biol, V39, P921
[2]   EXTENT OF FETAL OSSIFICATION AS AN INDEX OF DELAYED DEVELOPMENT IN TERATOGENIC STUDIES ON THE RAT [J].
ALIVERTI, V ;
BONANOMI, L ;
GIAVINI, E ;
LEONE, VG ;
MARIANI, L .
TERATOLOGY, 1979, 20 (02) :237-242
[3]  
ALVEREZ L, 1987, TERATOGENICITY UNPUB
[4]  
[Anonymous], 1971, Statistical Principles in Experimental Design
[5]   Effects of carbendazim on rat thyroid, parathyroid, pituitary and adrenal glands and their hormones [J].
Barlas, N ;
Selmanoglu, G ;
Koçkaya, A ;
Songür, S .
HUMAN & EXPERIMENTAL TOXICOLOGY, 2002, 21 (04) :217-221
[6]  
BERGMEYER HU, 1974, METHOD ENZYMAT AN, P1205
[7]  
BERGQUIST C, 1983, FERTIL STERIL, V39, P761
[8]  
BISHOP M L., 2000, Clinical Chemistry: Principles, Procedures, Correlations, VFourth
[9]  
BLADON P, 1958, BIOCH PATHOLOGY
[10]   MECHANISM OF ACTION OF COLCHICINE - BINDING OF COLCHINCINE-3H TO CELLULAR PROTEIN [J].
BORISY, GG ;
TAYLOR, EW .
JOURNAL OF CELL BIOLOGY, 1967, 34 (02) :525-&