Science and Technology Innovation Centre, Guangzhou University of Chinese Medicine, Guangzhou, China; Lingnan Medical Research Centre, Guangzhou University of Chinese Medicine, Guangzhou, China; The Second Affiliated Hospital, Guangzhou University of Chinese Medicine, Guangzhou, China.
Science and Technology Innovation Centre, Guangzhou University of Chinese Medicine, Guangzhou, China; Lingnan Medical Research Centre, Guangzhou University of Chinese Medicine, Guangzhou, China.
Eur J Pharmacol. 2020 Oct 5;884:173327. doi: 10.1016/j.ejphar.2020.173327. Epub 2020 Jul 26.
AIDS, a serious fatal disease caused by the human immunodeficiency virus (HIV), is an epidemic disease for which no effective vaccine has been established. The current therapeutic interventions for AIDS have limited efficacy because they are unable to clear HIV infections and the continuous occurrence of resistant HIV strains. Therefore, the exploitation of new drugs to prevent the spread of AIDS remains a high priority. In this study, the effects of icariin and its metabolite anhydroicaritin on SIV/HIV replication were investigated. In CEM × 174 cells and PBMC cells, both icariin and anhydroicaritin can significantly inhibit HIV-1 or SIVmac251 replication. Furthermore, molecular docking studies revealed that icariin and anhydroicaritin can act on both HIV reverse transcriptase and protease but could not bind to integrase. Reverse transcriptase and protease inhibition biological assays showed that both icariin and anhydroicaritin could significantly inhibit only HIV reverse transcriptase. In summary, the two compounds can significantly inhibit HIV/SIV in vitro and their targets may be mainly involved with HIV reverse transcriptase.
艾滋病,一种由人类免疫缺陷病毒(HIV)引起的严重致命疾病,是一种尚未建立有效疫苗的传染病。目前治疗艾滋病的干预措施疗效有限,因为它们无法清除 HIV 感染和不断出现的耐药 HIV 株。因此,开发新的药物来预防艾滋病的传播仍然是当务之急。在这项研究中,研究了淫羊藿苷及其代谢物脱水淫羊藿苷对 SIV/HIV 复制的影响。在 CEM×174 细胞和 PBMC 细胞中,淫羊藿苷和脱水淫羊藿苷均可显著抑制 HIV-1 或 SIVmac251 的复制。此外,分子对接研究表明,淫羊藿苷和脱水淫羊藿苷均可作用于 HIV 逆转录酶和蛋白酶,但不能与整合酶结合。逆转录酶和蛋白酶抑制生物测定表明,淫羊藿苷和脱水淫羊藿苷均可显著抑制仅 HIV 逆转录酶。综上所述,这两种化合物可显著抑制 HIV/SIV 体外,其靶点可能主要涉及 HIV 逆转录酶。