期刊文献+

槐定对互隔交链孢霉霉菌毒素所致DNA损伤的抑制作用 被引量:1

Inhibitory Effects of Sophoridine on DNA Damage Induced by the Mycotoxins of Alternaria alternata
下载PDF
导出
摘要 本文应用碱性洗脱荧光分析法探讨了槐定对互隔交链孢霉的两种毒素——交链孢酚单甲醚(AME)和交链孢酚(AOH)引起2BS细胞DNA单链断裂的抑制作用。实验结果表明,槐定能抑制AME和AOH引起的2BS细胞DNA单链断裂,加入不同浓度的槐定作用后洗脱9小时DNA在滤膜上的存留分数分别为:AME组,由对照组的0.205=0.02回升至0.57±0.02、0.61±0.05、0.74±0.03;AOH组,由对照组的0.11±0.01回升至0.45±0.04、0.58±0.03、0.85±0.06,实验组与对照组比较统计学处理均有显著差别(P<0.01)。 In this study, the alkaline elution and fluorometic DNA assay were used to explore the inhibitory effects of sophoridine on DNA damage induced by the alternariol monomethyl ether (AME) and alternariol (AOH) which were produced by alternaria alternata. The results showed that sophoridine was able to inhibit the DNA single-strand breaks induced by the AME and AOH in the cultured human fetal lung 2BS cells : (1)Under the sophoridine concentration of 12.5μg/ml,25μg/ml,50μg/ml,the fraction of DNA remaining on the filters in AME (50μg/ml) groups was 0.57±0. 02,0.61±0.05,0.74 ±0.03 respectively,while it was 0.20±0.02 in the control group (only with AME 50μg/ml). (2) Under the sophoridine concentration of 25μg/ml,50μg/ml, l00μg/ml,the fraction of DNA remaning on the filters in AOH (10μg/ml) groups was 0.45±0.04,0.58±0.03,0.85±0.06 respectively, while it was 0.11±0.01 in the control group (only with AOH 10μg/ml). The dosage-response relationships of both AME and AOH groups were clearly shown. The fraction of DNA remaining on the filters by test groups were significantly different from that by control gronps (P<0.01).
出处 《河南肿瘤学杂志》 1992年第1期25-28,共4页 Henan Journal of Oncology
关键词 链格孢霉 槐定 DNA损伤 肿瘤 alternaria mycotoxins sophoridine DNA single-strand
  • 相关文献

参考文献3

  • 1秦秀生,郑智敏,刘桂亭,钱玉珍,阮丽荣,苏堤,徐友梅,李雪梅,余月华.槐定的致突变性研究[J].河南肿瘤学杂志,1991,4(3):5-7. 被引量:3
  • 2张鹏,刘桂亭,甄应中,王秀林,安玉会,苗健.-3诱发人羊膜细胞UDS的研究[J]中国病理生理杂志,1986(04).
  • 3董伟华,刘桂亭,陈勇夫,郑智敏,甄应中,安玉会,苗健.运用体内、外结合检测方法对互隔交链孢霉诱变性的研究[J]癌症,1986(02).

二级参考文献2

  • 1董伟华,刘桂亭,陈勇夫,郑智敏,甄应中,安玉会,苗健.运用体内、外结合检测方法对互隔交链孢霉诱变性的研究[J]癌症,1986(02).
  • 2李在邠,赵德化,盛宝恒.槐定碱抗实验性心律失常作用[J]第四军医大学学报,1986(01).

共引文献2

同被引文献10

引证文献1

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