摘要
目的通过分析小檗碱处理后的Raji细胞中EB病毒DNA的变化,探讨小檗碱对EB病毒DNA复制的抑制作用。方法运用四甲基偶氮唑蓝法确定小檗碱对Raji细胞生长的细胞无毒性浓度,然后采用巢式荧光定量PCR方法检测该浓度处理后的Raji细胞EB病毒DNA含量,分析小檗碱对EB病毒DNA复制的影响。结果小檗碱对Raji细胞的细胞无毒性浓度(NCC)为0~10μmol/L.不同浓度(1.25、10和40μmol/L)的小檗碱处理后的Raji细胞EB病毒DNA拷贝数与未加药组相比显著降低(P<0.05),呈药物浓度依赖性。结论小檗碱在细胞无毒性浓度下,可抑制Raji细胞中EB病毒DNA的复制,为使用小檗碱或含小檗碱的中药复方防治EB病毒相关肿瘤提供了新的实验依据。
ObjectiveTo observe the effect of berberine (BBR) on EBV-DNA replication in Raji cells treated with BBR.MethodsMTT assay was used for determining non-cytotoxic concentration (NCC) of BBR in Raji cells. After being treated with BBR at NCC, EBV-DNA was detected by fluorescent quantitative nested-PCR, and then the inhibitory effect of BBR was analyzed on EBV-DNA replication in Raji cells at various concentrations.Results NCC of BBR in Raji cells was 0~10 μmol/L, EBV-DNA levels of Raji cells with BBR treatment at 1.25, 10 and 40μmol/L were obviously lower than that without using BBR (P 0.05).ConclusionBBR could inhibit EBV-DNA replication at NCC, it provides a new experimental evidence to prevent and cure nasopharyngeal carcinoma using BBR or the traditional Chinese drug compound recipes comprised of BBR.
出处
《中国现代医学杂志》
CAS
CSCD
北大核心
2010年第4期490-493,497,共5页
China Journal of Modern Medicine
基金
国家自然科学基金(30572455
30973400)
国家科技部"863"项目(No:2006AA02Z481)
湖南省科技厅计划项目(No:2009WK3060)