Herbal Medicine Research Centre, Institute for Medical Research, National Institutes of Health, Ministry of Health Malaysia, Shah Alam, Selangor, Malaysia.
BMC Complement Med Ther. 2024 Sep 11;24(1):333. doi: 10.1186/s12906-024-04628-6.
In early 2020, COVID-19 pandemic has mobilized researchers in finding new remedies including repurposing of medicinal plant products focusing on direct-acting antiviral and host-directed therapies. In this study, we performed an in vitro investigation on the standardized Marantodes pumilum extract (SKF7) focusing on anti-SARS-CoV-2 and anti-inflammatory activities.
Anti-SARS-CoV-2 potential of the SKF7 was evaluated in SARS-CoV-2-infected Vero E6 cells and SARS-CoV-2-infected A549 cells by cytopathic effect-based assay and RT-qPCR, respectively. Target based assays were performed on the SKF7 against the S1-ACE2 interaction and 3CL protease activities. Anti-inflammatory activity of the SKF7 was evaluated by nitric oxide inhibitory and TLR2/TLR4 receptor blocker assays.
The SKF7 inhibited wild-type Wuhan (EC of 21.99 µg/mL) and omicron (EC of 16.29 µg/mL) SARS-CoV-2 infections in Vero-E6 cells. The SKF7 also inhibited the wild-type SARS-CoV-2 infection in A549 cells (EC value of 6.31 µg/mL). The SKF7 prominently inhibited 3CL protease activity. The SKF7 inhibited the LPS induced-TLR4 response with the EC of 16.19 µg/mL.
In conclusion, our in vitro study highlighted anti-SARS-CoV-2 and anti-inflammatory potentials of the SKF7. Future pre-clinical in vivo studies focusing on antiviral and immunomodulatory potentials of the SKF7 in affecting the COVID-19 pathogenesis are warranted.
2020 年初,COVID-19 大流行促使研究人员寻找新的治疗方法,包括重新利用药用植物产品,重点关注直接作用的抗病毒和宿主导向疗法。在这项研究中,我们对标准化的 Marantodes pumilum 提取物(SKF7)进行了体外研究,重点研究其抗 SARS-CoV-2 和抗炎活性。
通过细胞病变效应测定法和 RT-qPCR 分别在 SARS-CoV-2 感染的 Vero E6 细胞和 SARS-CoV-2 感染的 A549 细胞中评估 SKF7 的抗 SARS-CoV-2 潜力。针对 S1-ACE2 相互作用和 3CL 蛋白酶活性进行基于靶标的测定。通过一氧化氮抑制和 TLR2/TLR4 受体阻断测定法评估 SKF7 的抗炎活性。
SKF7 抑制了野生型武汉(EC 为 21.99μg/mL)和奥密克戎(EC 为 16.29μg/mL)SARS-CoV-2 在 Vero-E6 细胞中的感染。SKF7 还抑制了 A549 细胞中的野生型 SARS-CoV-2 感染(EC 值为 6.31μg/mL)。SKF7 显著抑制 3CL 蛋白酶活性。SKF7 抑制 LPS 诱导的 TLR4 反应,EC 值为 16.19μg/mL。
总之,我们的体外研究强调了 SKF7 的抗 SARS-CoV-2 和抗炎潜力。未来有必要进行针对 SKF7 的抗病毒和免疫调节潜力的临床前体内研究,以影响 COVID-19 的发病机制。