泰国草药提取物 Kerra™ 的抗人类免疫缺陷病毒-1 特性

Pharmaceuticals Pub Date : 2024-07-09 DOI:10.3390/ph17070917
Siriwan Saehlee, Supaphorn Seetaha, Wiwat Klankaew, Pussadee Srathong, K. Choowongkomon, Khuanjarat Choengpanya
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引用次数: 0

摘要

Kerra™ 是一种泰国传统草药,源自《Tak-Ka-Si-La 经》,由九种药用植物组成,具有潜在的抗 HIV 病毒特性。本研究调查了 Kerra™ 对 HIV-1 逆转录酶(RT)的抑制作用及其在 HEK293 细胞中预防假性 HIV 病毒感染的能力。结果表明,Kerra™ 提取物对 HIV-1 RT 的相对抑制率为 95.73 ± 4.24%,IC50 值为 42.66 ± 8.74 µg/mL。对接研究显示,Kerra™中的主要植物化学物质,如油酰胺、甲萘素和生物香豆素A,与RT非核苷结合袋中的几个残基相互作用,从而产生抑制作用。此外,当 Kerra™ 的浓度为 10 µg/mL 时,它还能减少 HEK293 细胞中的假性 HIV 感染,这表明它具有作为 HIV 辅助疗法的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anti-Human Immunodeficiency Virus-1 Property of Thai Herbal Extract Kerra™
Kerra™, a Thai traditional herbal medicine derived from the “Tak-Ka-Si-La Scripture” and composed of nine medicinal plants, has demonstrated potential antiviral properties against HIV. This study investigated the inhibitory effects of Kerra™ on HIV-1 reverse transcriptase (RT) and its ability to prevent pseudo-HIV viral infection in HEK293 cells. The results showed that Kerra™ extract achieved a 95.73 ± 4.24% relative inhibition of HIV-1 RT, with an IC50 value of 42.66 ± 8.74 µg/mL. Docking studies revealed that key phytochemicals in Kerra™, such as oleamide, formononetin, and biochanin A, interact with several residues in the RT non-nucleoside binding pocket, contributing to their inhibitory effects. Furthermore, Kerra™ was able to reduce pseudo-HIV infection in HEK293 cells at a concentration of 10 µg/mL, suggesting its potential as a supplementary treatment for HIV.
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