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萘对大鼠致畸实验 被引量:1

Study on the Teratogenic Effect of Naphthalene in SD Rats
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摘要 将妊娠大鼠随机分为5组,即敌枯双1mg/kg·d^(-1)(阳性对照组)、空白乳剂(阴性对照组)、萘实验组1000mg/kg·d^(-1)、600mg/kg·d^(-1)和60mg/kg·d^(-1),分别在怀孕第6~15d经灌胃给药。实验结果:萘为1000mg/kg·d^(-1)和600mg/kg·d^(-1)剂量组的母鼠和仔鼠均体重减轻,影响仔鼠的发育,某些骨骼发生骨化迟缓(胸骨和枕骨)。在1000mg/kg·d^(-1)组早期吸收胎和死胎发生率增加,但未发现畸形仔鼠。60mg/kg·d^(-1)组和阴性对照组经统计学处理无显著性差异,母鼠和仔鼠均无任何影响。阳性对照组则有明显的致畸作用。认为萘对大鼠不是一种致畸原。 Pregnant SD rats were divided into 5 groups randomly, ie N, N'-methylene-Bis (2-Amino 1, 2, 4-Thiadiazole) 1mg/kg·d^(-1) (positive control), blank emulsion (negative control), and naphthalene 1000mg/kg·d^(-1),600mg/kg·d^(-1) & 60mg/kg·d^(-1),and were administered by gastric intubation daily within 6 to 15d of the pregnancy. The results of experiments demonstrated that naphthalene dose at 600mg/kg·d^(-1) & 1000mg/kg·d^(-1) both maternal body weight gain &embryo fetal development were depressed, and ossification of some parts of the skeletal districts (Sternum & occipital bone)were retarded. At 1000mg/kg·d^(-1) increased embryo absorption and death rate were found, but no malformed fetus. There were not any statistical difference between the naphthalene 60mg/kg·d^(-1) group & the negative control group, neither the dam nor the fetuses were affected. Pregnant rats of positive control group showed obvious teratogenic effects. It may be concluded that naphthalene is not a teratogen of rat.
出处 《安徽医科大学学报》 CAS 1989年第1期16-19,共4页 Acta Universitatis Medicinalis Anhui
关键词 致畸胎物 妊娠 中毒 大鼠 pregnancy animal, laboratory teratogens naphthalenes poisoning
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  • 1黄正,王家玲.细菌发光试验及Ames试验检测工业废水急性毒性及致突变性的研究[J].环境科学,1994,15(6):70-71. 被引量:11
  • 2王献仁,尹先仁,郭润荣,张丽霞.萘丸吸入毒性研究[J].环境与健康杂志,1995,12(2):67-68. 被引量:6
  • 3陈逖.139名萘作业工人眼病情况调查[J].安徽医科大学学报,1990,25(2):130-130.
  • 4Sarojini R. Naphthalene - induced atresia in the ovary of the crayfish,Procambarus clarkii. Ecotoxicol Environ Saf, 1995, 31(1):76.
  • 5Iyer P. Role of biotransformation in the in vitro preimplantation embryotoxicity of naphthalene. Toxicology, 1991, 66 (3):257 - 270.
  • 6Virchows Archiv fuer Pathologische, Anatonie und Physiologie, und fuer Klinische Medizin. (Berlin, Ger) V.1 -343, 1847- 1967.For publisher information, see VAAPB7. 1956, 329:141.
  • 7Kanekal S.Metabolism and cytotodcity of naphthalene oxide in the isolated perfused mouse lung. J Pharmacol Exp Ther, 1991, 256( 1 ): 391.
  • 8Hakura A.Mutagenicity and cytotoxicity of naphthoquinones for Ames Salmonella. Chem Res Toxicol, 1994, 7 (4):559.
  • 9Chichester CH. Metabolism and cytotoxicity of naphthalene and its metabolites isolated muine Clara cells. Mol Phamaccol, 1994, 45(4) :664.
  • 10Tsuruda LS.Fornation of epoxide and quinone protein adducts in B6C3F1 micetreated with naphthalene, sulfate conjugate of 1, 4 - dihydroxynaphthalene and 1, 4 - naphthoquinone. Arch Toxicol, 1995,69 (6) :362- 367.

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