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甘草酸对人类免疫缺陷病毒(HIV)复制的抑制作用机制。

Mechanism of inhibitory effect of glycyrrhizin on replication of human immunodeficiency virus (HIV).

作者信息

Ito M, Sato A, Hirabayashi K, Tanabe F, Shigeta S, Baba M, De Clercq E, Nakashima H, Yamamoto N

机构信息

Department of Bacteriology, Fukushima Medical College, Japan.

出版信息

Antiviral Res. 1988 Dec 11;10(6):289-98. doi: 10.1016/0166-3542(88)90047-2.

Abstract

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.

摘要

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。

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