Histological and histomorphometric alterations in thyroid and adrenals of CD rat pups exposed in utero to methyl thiophanate

被引:31
作者
Maranghi, F [1 ]
Macrì, C [1 ]
Ricciardi, C [1 ]
Stazi, AV [1 ]
Rescia, M [1 ]
Mantovani, A [1 ]
机构
[1] Ist Super Sanita, Comparat Toxicol & Ecotoxicol Lab, I-00161 Rome, Italy
关键词
thyroid; adrenals; endocrine disrupters; development; fungicide; rat; postnatal effects; prenatal exposure;
D O I
10.1016/S0890-6238(03)00105-9
中图分类号
Q [生物科学];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
Pregnant CD rats were treated with an initial dose of 0, 310 or 560 mg/kg bw per day of the fungicide methyl thiophanate (MT) on gestational days 10-14, corresponding to formation of thyroid and adrenal primordia; newborns were sacrificed on postnatal days (PNDs) 10 and 23. No apparent maternal toxicity and no effects on litter size, viability or weight gain were present. Delayed ear pinna detachment and eye opening were present at top dose level. Thyroid histology showed increased irregular nuclei and/or mitoses (PND 10-both doses), cells with necrotic or hydropic changes (PND 23-top dose). The adrenal cortex showed increased karyomegaly and hydropic degeneration (PND 23-both doses). Thyroid histomorphometry showed reduced follicular density, moderately increased follicular cell height and number of nuclei/follicle (PND 10-top dose and PND 23-both doses), suggesting retarded follicular maturation. The adrenal cortex relative area was slightly decreased (PND 10-top dose and PND 23-both doses). MT may act as weak endocrine disrupter, suggesting that attention should be paid to delayed endocrine alterations elicited by agrochemicals. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:617 / 623
页数:7
相关论文
共 29 条
[1]
Occupational and environmental agents as endocrine disrupters: Experimental and human evidence [J].
Baccarelli, A ;
Pesatori, AC ;
Bertazzi, PA .
JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, 2000, 23 (11) :771-781
[2]
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
[3]
Fetal origins of cardiovascular disease [J].
Baum, M ;
Ortiz, L ;
Quan, A .
CURRENT OPINION IN PEDIATRICS, 2003, 15 (02) :166-170
[4]
EFFECTS OF METHYL BENZIMIDAZOLECARBAMATE DURING EARLY-PREGNANCY IN THE RAT [J].
CUMMINGS, AM ;
HARRIS, ST ;
REHNBERG, GL .
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1990, 15 (03) :528-535
[5]
Impact of exposure to endocrine disrupters in utero and in childhood on adult reproduction [J].
Damgaard, IN ;
Main, KM ;
Toppari, J ;
Skakkebæk, NE .
BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM, 2002, 16 (02) :289-309
[6]
Screening methods for thyroid hormone disruptors [J].
DeVito, M ;
Biegel, L ;
Brouwer, A ;
Brown, S ;
Brucker-Davis, F ;
Cheek, AO ;
Christensen, R ;
Colborn, T ;
Cooke, P ;
Crissman, J ;
Crofton, K ;
Doerge, D ;
Gray, E ;
Hauser, P ;
Hurley, P ;
Kohn, M ;
Lazar, J ;
McMaster, S ;
McClain, M ;
McConnell, E ;
Meier, C ;
Miller, R ;
Tietge, J ;
Tyl, R .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1999, 107 (05) :407-415
[7]
Endocrine active agents: Implications of adverse and non-adverse changes [J].
Foster, PMD ;
McIntyre, BS .
TOXICOLOGIC PATHOLOGY, 2002, 30 (01) :59-65
[8]
Furness PN, 1997, J PATHOL, V183, P253, DOI 10.1002/(SICI)1096-9896(199711)183:3<253::AID-PATH927>3.0.CO
[9]
2-P
[10]
Xenoendocrine disrupters-tiered screening and testing Filling key data gaps [J].
Gray, LE ;
Ostby, J ;
Wilson, V ;
Lambright, C ;
Bobseine, K ;
Hartig, P ;
Hotchkiss, A ;
Wolf, C ;
Furr, J ;
Price, M ;
Parks, L ;
Cooper, RL ;
Stoker, TE ;
Laws, SC ;
Degitz, SJ ;
Jensen, KM ;
Kahl, MD ;
Korte, JJ ;
Makynen, EA ;
Tietge, JE ;
Ankley, GT .
TOXICOLOGY, 2002, 181 :371-382