期刊文献+

子宫实验和E-SCREEN实验在检测雌激素活性中的相关性 被引量:9

Correlation comparison of uterotrophic assay and E-SCREEN assay for estrogenic activities
下载PDF
导出
摘要 目的 以 1 7β 雌二醇 (1 7β E2 )和四种植物提取物为受试物 ,研究子宫实验和E SCREEN实验在检测雌激素活性中的相关性。方法 断乳雌性小鼠 (1 0~ 1 2g)按体重分为 6组 ,分别给予小茴香、山豆根、补骨脂和川牛膝提取物 (1 0g kgBW ,ig)、1 7β E2 (0 5mg kgBW ,sc)和蒸馏水 (ig) ,持续 9天后处死动物剥离子宫称重。分别在人类乳腺癌MCF 7细胞培养液中加入四种植物提取物 (终浓度 1 0mg L)和 1 7β E2 (终浓度0 3μmol L) ,计算各组细胞在 1 2 0h内的平均群体倍增时间 ,分析小鼠子宫重量与细胞群体倍增时间的相关性。结果  4种植物提取物均可使小鼠子宫重量增加 (P <0 0 5或P <0 0 1 ) ,细胞群体倍增时间缩短。子宫重量与群体倍增时间呈显著负相关 (r=- 0 96 7,P <0 0 1 )。结论 子宫实验和E Objective To evaluate the correlation of uterotrophic assay in immature mice and E SCREEN assay for estrogenic activities using 17β estradiol (17β E 2) and four botanical extracts ( Fructus Foeniculi, Fructus Psoraleae, Radix Cyathulae and Radix Sophorae Tonkinensis). Methods Weanling female Kunming mice weighed 10-12g were given botanical extracts (10 g/kg BW, i.g) and 17β E 2 (0 5 mg/kg BW, s.c), respectively, for 9 days. Uterine and ovary weights of mice were measured after killed. Human breast cancer MCF 7 cells were cultured and treated with botanical extracts (final concentration: 10 mg/L) and 17β E 2(final concentration: 0 3μmol/L) for 120 h, respectively. The doubling time of cell growth was calculated and analyzed its correlation with average uterine weights obtained from uterotrophic assay. Results Four botanical extracts, as well as 17β E 2, increased uterine weights of mice significantly ( P <0 05 or P <0 01) and shortened the doubling time of cell growth. And uterine weights were inversely correlated with the doubling time of cell growth ( r =-0 967, P <0 01) Conclusion The result of uterotrophic assay in immature mice was consistent with that of E SCREEN assay when evaluating estrogenic activities.
出处 《卫生研究》 CAS CSCD 北大核心 2004年第4期458-460,共3页 Journal of Hygiene Research
关键词 子宫实验 E-SCREEN实验 雌激素活性 相关性 uterotrophic assay, E-SCREEN assay, estrogenic activity, correlation
  • 相关文献

参考文献9

  • 1[1]Andersen HR, Andersson AM, Arnold SF, et al. Comparison of shortterm estrogenicity tests for identification of hormone-disrupting chemicals.Environ Health Perspect, 1999,107(S1): 89-108
  • 2[2]Padilla-Banks E, Jefferson WN, Newbold RR. The immature mouse is a suitable model for detection of estrogenicity in the uterotropic bioassay.Environ Health Perspect, 2001, 109:821-826
  • 3[3]Korach KS, McLachlan JA. Techniques for detection of estrogenicity.Environ Health Perspect, 1995, 103(S7): 5-8
  • 4[4]Villalobos M, Olea N, Brotons JA, et al. The E-Screen assay: a comparison of different MCF-7 cell stocks. Environ Health Perspect,1995, 103 (9): 844-850
  • 5[5]Soto AM, Sonnenschein C, Chung KL, et al. The E-SCREEN assay as a tool to identify estrogens: an update on estrogenic environmental pollutants. Environ Health Perspect, 1995, 103(S7): 113-122
  • 6[6]Diel P, Smolnikar K, Michan H. In vitro test systems for the evaluation of the estrogenic activity of natural products. Planta Medica, 1999, 65:197-203
  • 7[7]Zugmaier G, Knabee C, Fritsch C, et al. Tissue culture condition determinate the effects of estrogen and growth factors on anchorage independent growth of human breast cancer cell lines. J Steroid Biochem Mol Biol, 1991, 39:681-685
  • 8[8]Fang H, Tong W, Perkins R, et al. Quantitative comparisons of in vitro assays for estrogenic activities. Environ Health Perspect, 2000, 108:723-729
  • 9史琳娜,苏宜香.大豆异黄酮类对去卵巢大鼠骨丢失的影响[J].营养学报,2000,22(2):113-118. 被引量:49

二级参考文献1

共引文献48

同被引文献194

引证文献9

二级引证文献141

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部