恩替卡韦
乙型肝炎表面抗原
病毒学
重组DNA
HBeAg
乙型肝炎病毒
拉米夫定
医学
生理盐水
核苷酸
病毒
生物
内科学
基因
生物化学
作者
Guojing Wang,Gang Wang,Xiaoyan Dong,Wenhong Tian,Jie Yuchi,Guochao Wei,Hong Meng,Xiaobing Wu
出处
期刊:PubMed
日期:2013-01-01
卷期号:29 (1): 95-106
被引量:5
摘要
We evaluated the anti-HBV effects of nucleotide analogues, Entecavir (ETV) and Lamivudine (LAM) targeting mouse model of HBV persistent infection with recombinant adeno-associated virus 8 carrying 1.3 copies of HBV genome (rAAV8-1.3HBV). Ninety percent (27 of 30 mice) of rAAVS-treated mice were chosen as mouse model. Four groups were orally administrated with different doses of ETV (1 mg/(kgd) or 0.1 mg/(kgd)) and LAM (500 mg/(kgd) or 100 mg/(kgd)) once a day for 10 days. The other two groups were set as normal saline treated and untreated control. We detected the levels of HBV DNA, HBeAg and HBsAg in sera at different time. Results indicate that HBV DNA level decreased significantly (P < 0.05) in drug-treated groups compared with normal saline group after drug administration. Fifteen days after the drug withdrawal, HBV DNA level rebounded back obviously (P < 0.05) in groups with low doses of ETV and LAM. However, there was no apparent change of HBeAg and HBsAg in the whole process among all groups. These results showed that our model could reflect the anti-viral effect of nucleotide analogues. This model can be a useful and convenient tool for anti-HBV drug discovery.
科研通智能强力驱动
Strongly Powered by AbleSci AI