摘要
目的探讨长期服用阿德福韦酯对CHB患者外周血单个核细胞(PBMCs)线粒体的可能损伤。方法本研究包括18例服用阿德福韦酯2年、25例服用3年和22例未服用阿德福韦酯的CHB患者;采用实时定量PCR法检测各组患者PBMCs中线粒体DNA(mtDNA)含量(mtDNA/nDMA);采用ELISA法检测血浆丙二醛(MDA)、F2-isoprostanes含量;采用分光光度法检测血浆总抗氧化能力(TAOC)。结果 2年组患者mtDNA含量为0.6±0.4copies/cell,3年组为0.8±0.5copies/cell,均显著低于对照组(1.4±1.2 copies/cell,P均<0.05);2年组F2-iso-prostanes含量为1.5±0.8ng/ml,3年组为2.2±1.3ng/ml,显著低于对照组(3.7±2.7ng/ml,P均<0.05);2年组TAOC含量为3.0±1.1单位/毫升,3年组为2.3±1.4单位/毫升,显著低于对照组(4.3±1.8单位/毫升,P均<0.05)。3组间MDA含量无统计学差异(F=2.404,P>0.05)。结论长期应用阿德福韦酯治疗慢性乙型肝炎,对PBMCs中mtDNA水平有一定的影响,其意义还有待探讨。
Objective To observe the changes of mitochondrial DNA levels in peripheral blood monouclear cells in patients with chronic hepatitis B receiving long-term adefovir treatment.Methods Patients with CHB were divided into three groups:(1) 2 years group(n=18):receiving adefovir for 2 years;(2)3 years group (n=25):adefovir for 3 years;and (3) control group(n=22):naive patients without antiviral treatment.The mtDNA of PBMCs were detected by quantitative real-time PCR. Plasma MDA and F2-isoprostanes were measured by ELISA and TAOC were detected by spectrophotometry.Results The mtDNA in PBMCs in the 2-year treatment group was 0.6+0.4 copies/cell and in the 3-year treatment group was 0.8-+0.5 copies/cell,both signifieantly lower than in the control group (1.4±1.2copies/cell,P〈0.05);thc F2-isoprostanes in 2-year treatment group was 1.5±0.8 ng/ml and in 3-year treatment group was 2.2±1.3ng/ml,much lower than that in the control group(3.7±2.7 ng/ml,P〈0.05);the TAOC in 2-year treatment group was 3.0±1.1 IU/ml,and in 3-year treatment group was 2.3±l.4IU/ml, significantly lower than in the control group (4.3±1.8 IU/ml,P〈0.05).Conclusion The long-term administration of adefovir might injure mitochondrial DNA.
出处
《实用肝脏病杂志》
CAS
2012年第1期10-13,共4页
Journal of Practical Hepatology
基金
北京市丰台区科技项目(项目编号xm101210)
中国艾滋病和结核病多学科应用培训项目(编号5U2RTW006918-08)