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丙烯酰胺对雄性小鼠生殖系统的影响 被引量:3

Effect of Acrylamide Monomer on Genital System of Male Mice
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摘要 本文运用睾丸染色体畸变试验和精子畸形试验研究了丙烯酰胺对雄性小鼠生殖系统的影响。试验组剂量分别为21.25、42.5、85mg/kg。丙烯酰胺所致的畸变最低剂量精原细胞为85mg/kg,精母细胞和精子畸形均为42.5mg/kg,并有一定的剂量-反应关系。实验结果表明丙烯胺中剂量和高剂量能引起生殖细胞畸变和精子畸形,但低剂量组(21.25mg/kg)未见明显的致突变作用。 In this paper, the effects of anrylamide mo- nomer on genital system in male mice was stu- died by means of sperm morphology and chro- mosomal aberrations in germ cells of testis. Male mice were given the acrylamide monomer in doses of 21.25, 42.5, 85mg/kg by intraperito- heal injection. The least dose of acrylamide monomer was 85mg/kg for the mutagenic induct- ion of spermatogonia, 42.5mg/kg for that of pr- imary spermatocyte and sperm shape. There was a difinite relationship between dose and re- sponse. The result indicated that acrylarnide m- onomer was mutagenic to germ cells and sperm of testis in middle and high dose while no sign- ificant mutagencity was found at lower exposu- re level (21,25mg/kg).
出处 《中国公共卫生学报》 1993年第1期33-35,共3页
关键词 丙烯酰胺 生殖系统 染色体 精子 Acrylamide monomer Spermshape abnormality Chromosomal aberration
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同被引文献60

  • 1邓春华,郭海彬,刘建中.老年大鼠睾丸间质细胞结构和功能变化的实验研究[J].中华男科学杂志,2005,11(10):740-743. 被引量:12
  • 2王皓,葛津瑶,周振琪,王正朝,石放雄.口服丙烯酰胺对雄性大鼠生长发育及生殖机能的影响[J].中华男科学杂志,2007,13(6):492-497. 被引量:16
  • 3Xie Q, Sun H, Liu Y, et al. Adduction of biomacromolecules with acrylamide (AA) in mice at environmental dose levels studied by acceleratormass spectrometry. ToxicolLett, 2006,163 : 101-108.
  • 4Sumizawa T, Igisu H. Release of heat shock proteins from human neuroblastoma cells exposed to acrytamide. J. Toxicol. Sci, 2008,33 : 117-122.
  • 5Mottram DS, Wedzicha BL, Dodson AT. Acrylamide is formed in the Maillard reaction. Nature, 2002,419:448- 449.
  • 6Stadler RH, Blank I, Varga N. Aerylamide from Maillard reaction products. Nature, 2002,419 : 449-450.
  • 7Ghanayem BI, Witt KL, Hadri EL, et al. Comparison of germ cell mutagenicity in male CYP2EI-mull and wildtype mice treated with acrylamide: evidence supporting a glycidamide-mediated effect. Biol Reproduct, 2005,72: 157-163.
  • 8Carere A. Genotoxicity and carcinogenicity of acrylamide: a critical review. Ann Ist Super Sanita, 2006,42:144-155.
  • 9Fuhr U, Boettcher MI, Schippers MK, et al. Toxicokinetics of acrylamide in humans after ingestion of a defined dose in a test meal to improve risk assessment for acrylamide carcinogenicity. Cancer Epidemiology Biomarkers & Prevention, 2006,15 : 266-271.
  • 10Fennell TR, Friedman MA. Comparision Of Acrylamide metabolism in humans and rodents. Chemistry and Safety of Acrylamid in Food, 2005.109-116.

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