Developmental toxicity of triphenyltin hydroxide in mice

被引:16
作者
Sarpa, Marcia
De-Carvalho, Rosangela R.
Delgado, Isabella F.
Paumgartten, Francisco J. R.
机构
[1] Fundacao Oswaldo Cruz, Natl Sch Publ Hlth, Dept Biol Sci, Lab Environm Toxicol, BR-21040361 Rio De Janeiro, Brazil
[2] Fundacao Oswaldo Cruz, Natl Inst Hlth Qual Control, Dept Immunol, BR-21040361 Rio De Janeiro, Brazil
关键词
fentin hydroxide; TPTH; organotin compounds; pre-natal toxicity; teratogenicity; embryotoxicity;
D O I
10.1016/j.yrtph.2007.05.006
中图分类号
DF [法律]; D9 [法律]; R [医药、卫生];
学科分类号
0301 ; 10 ;
摘要
Triphenyltin-hydroxide (TPTH) is used as agricultural fungicide in Brazil and elsewhere. This study was undertaken to evaluate the developmental toxicity of TPTH in mice. Swiss Webster mice were treated by gavage with TPTH (0, 3.75, 7.5, 15 and 30 mg/kg bw/day) on gestation days (GD) 6-17. Caesarean sections were performed on GD 18, and implantations, resorptions and live and dead fetuses were counted. Half of each litter was fixed and examined for visceral anomalies while the remaining fetuses were cleared and stained with Alizarin Red S for skeleton evaluation. A reduced pregnancy weight gain (after subtraction of uterine weights), smaller thymus, spleen and liver, and deaths indicated that doses >= 7.5 mg/kg body wt/day were toxic to mothers. At the two highest doses, TPTH enhanced embryolethality and reduced fetal body weight. The incidence of cleft palate (not seen in controls) was augmented (36.8%) at the highest dose of TPTH, while palatine bone defects were increased at the lowest dose (3.75 mg/kg bw/day). Soft-tissue anomalies, such as misshapened thymus, and malpositioned testes and uteri, were more frequent at doses of TPTH >= 7.5 mg/kg bw/day. TPTH also caused a dose-related increase of fetal skeleton variations (e.g. poorly ossified skull bones) and malformations (misshapened Axis and skull bones). In conclusion, TPTH was toxic to the embryos (NOAEL < 3.75 mg/kg bw/day) at doses that were not overtly toxic to their mothers. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:43 / 52
页数:10
相关论文
共 34 条
  • [1] Effects of in utero tributyltin chloride exposure in the rat on pregnancy outcome
    Adeeko, A
    Li, DM
    Forsyth, DS
    Casey, V
    Cooke, GM
    Barthelemy, J
    Cyr, DG
    Trasler, JM
    Robaire, B
    Hales, BF
    [J]. TOXICOLOGICAL SCIENCES, 2003, 74 (02) : 407 - 415
  • [2] [Anonymous], 1999, CONC INT CHEM ASS DO
  • [3] *ANVISA, 2006, MON PROD AGR
  • [4] Organotin compounds: Toxicokinetic aspects
    Appel, KE
    [J]. DRUG METABOLISM REVIEWS, 2004, 36 (3-4) : 763 - 786
  • [5] [ATSDR. Agency for Toxic Substances and Disease Registry U. S. Department of Health and Human Services.], 2005, TOX PROF TIN TIN COM
  • [6] EMBRYOTOXIC EVALUATION OF BIS (TRI-NORMAL-BUTYLTIN)OXIDE (TBTO) IN MICE
    BARONCELLI, S
    KARRER, D
    TURILLAZZI, PG
    [J]. TOXICOLOGY LETTERS, 1990, 50 (2-3) : 257 - 262
  • [7] Bis(tributyltin) oxide toxicology
    Benya, TJ
    [J]. DRUG METABOLISM REVIEWS, 1997, 29 (04) : 1189 - 1284
  • [9] Classification terms in developmental toxicology: Need for harmonisation - Report of the Second Workshop on the Terminology in Developmental Toxicology Berlin, 27-28 August 1998
    Chahoud, I
    Buschmann, J
    Clark, R
    Druga, A
    Falke, H
    Faqi, A
    Hansen, E
    Heinrich-Hirsch, B
    Hellwig, J
    Lingk, W
    Parkinson, M
    Paumgartten, FJR
    Pfeil, R
    Platzek, T
    Scialli, AR
    Seed, J
    Stahlmann, R
    Ulbrich, B
    Wu, XD
    Yasuda, M
    Younes, M
    Solecki, R
    [J]. REPRODUCTIVE TOXICOLOGY, 1999, 13 (01) : 77 - 82
  • [10] PRENATAL OR POSTNATAL EXPOSURE TO BIS(TRI-NORMAL-BUTYLTIN)OXIDE IN THE RAT - POSTNATAL EVALUATION OF TERATOLOGY AND BEHAVIOR
    CROFTON, KM
    DEAN, KF
    BONCEK, VM
    ROSEN, MB
    SHEETS, LP
    CHERNOFF, N
    REITER, LW
    [J]. TOXICOLOGY AND APPLIED PHARMACOLOGY, 1989, 97 (01) : 113 - 123