Ito M, Sato A, Hirabayashi K, Tanabe F, Shigeta S, Baba M, De Clercq E, Nakashima H, Yamamoto N
Department of Bacteriology, Fukushima Medical College, Japan.
Antiviral Res. 1988 Dec 11;10(6):289-98. doi: 10.1016/0166-3542(88)90047-2.
Glycyrrhizin (GL) achieved a dose-dependent inhibition of the replication of human immunodeficiency virus type 1 (HIV-1) in MOLT-4 (clone No. 8) cells within the concentration range of 0.075 to 0.6 mM. Within this concentration range, GL also effected a dose-dependent reduction in the protein kinase C (PKC) activity of MOLT-4 (clone No. 8) cells. A well-known PKC inhibitor, 1-(5-isoquinolinesulfonyl)-2-methylpiperazine dihydrochloride (H-7), also proved inhibitory to HIV-1 replication in MOLT-4 (clone No. 8) cells. PKC inhibition may thus be considered as one of the mechanisms by which GL inhibits HIV-1 replication. In addition, GL may also owe its anti-HIV-1 activity, at least in part, to an interference with virus-cell binding, since the compound at 1.2 mM partially inhibited the adsorption of radiolabeled HIV-1 particles to MT-4 cells. At this concentration GL also suppressed giant cell formation induced by co-culturing MOLT-4 (clone No. 8) cells with MOLT-4/HTLV-IIIB cells, whereas the PKC inhibitor H-7 failed to do so.
甘草甜素(GL)在0.075至0.6 mM的浓度范围内,对MOLT-4(8号克隆)细胞中1型人类免疫缺陷病毒(HIV-1)的复制具有剂量依赖性抑制作用。在此浓度范围内,GL还使MOLT-4(8号克隆)细胞的蛋白激酶C(PKC)活性呈剂量依赖性降低。一种著名的PKC抑制剂,1-(5-异喹啉磺酰基)-2-甲基哌嗪二盐酸盐(H-7),也被证明对MOLT-4(8号克隆)细胞中的HIV-1复制具有抑制作用。因此,PKC抑制可能被认为是GL抑制HIV-1复制的机制之一。此外,GL的抗HIV-1活性至少部分可能归因于其对病毒与细胞结合的干扰,因为1.2 mM的该化合物可部分抑制放射性标记的HIV-1颗粒吸附到MT-4细胞上。在此浓度下,GL还抑制了将MOLT-4(8号克隆)细胞与MOLT-4/HTLV-IIIB细胞共培养所诱导的巨细胞形成,而PKC抑制剂H-7则无此作用。