Baicalin, an inhibitor of HIV-1 production in vitro

被引:150
作者
Kitamura, K
Honda, M
Yoshizaki, H
Yamamoto, S
Nakane, H
Fukushima, M
Ono, K
Tokunaga, T
机构
[1] Natl Inst Infect Dis, AIDS Res Ctr, Tokyo 162, Japan
[2] Aichi Canc Ctr, Res Inst, Lab Viral Oncol, Chikusa Ku, Nagoya, Aichi 464, Japan
[3] Aichi Canc Ctr Hosp, Dept Internal Med, Chikusa Ku, Nagoya, Aichi 464, Japan
关键词
baicalin; PBMC; reverse transcriptase inhibition; HIV-1;
D O I
10.1016/S0166-3542(97)00069-7
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The flavonoid baicalin markedly inhibits replication of human immunodeficiency virus type 1 (HIV-1) in a concentration-dependent manner in normal peripheral blood mononuclear cells (PBMC) stimulated with phytohemagglutinin (PHA) in vitro. The effect was more pronounced when the cells were pretreated with baicalin. Furthermore, baicalin inhibits HIV-1 replication in PHA-stimulated PBMC from asymptomatic HIV-1-seropositive carriers. The 50% inhibitory concentration for HIV-1 replication was approximately 0.5 mu g/ml. At the concentration of 2 mu g/ml of baicalin, copy numbers of HIV-1 proviral DNA were approximately 50 times less than in untreated controls. In a cell-free infection system, baicalin inhibited the activity of HIV-1 reverse transcriptase (RT), but not the activity of human DNA polymerases alpha and gamma (DNA polymerase beta was slightly inhibited), suggesting that the anti-HIV-1 effect of baicalin may at least partly be due to inhibition of HIV-1 RT. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:131 / 140
页数:10
相关论文
共 33 条
  • [31] YAMAGUCHI M, 1980, J BIOL CHEM, V255, P7002
  • [32] YARCHOAN R, 1986, LANCET, V1, P575
  • [33] YARCHOAN R, 1988, LANCET, V1, P76