Mukherjee Saikat, Tripathi Anusri
Department of Biochemistry and Medical Biotechnology, Calcutta School of Tropical, Medicine, Kolkata, West Bengal, India.
Department of Biochemistry and Medical Biotechnology, Calcutta School of Tropical, Medicine, Kolkata, West Bengal, India.
Eur J Med Chem. 2025 Jun 5;290:117536. doi: 10.1016/j.ejmech.2025.117536. Epub 2025 Mar 20.
Currently, there are no clinically approved antiviral agents against dengue-virus (DENV). This study aimed to determine the prophylactic, antiviral, and therapeutic potential of quercetin by its pre-treatment, co-treatment, and post-treatment [24, 48, and 72 h-post-infection (HPI)] of DENV-infected Balb/C mice through both oral and intraperitoneal (I.P) route, respectively. 80 mg/kg/day and 16 mg/kg/day of quercetin were non-toxic for oral and I.P administration, respectively. I.P. was found to be more effective than oral administration which significantly reduced DENV copy-number in co-treatment group (from day 1, p < 0.01); post-treatment (24hpi),and pretreatment groups (day 3 onwards, p < 0.05). Molecular-docking experiments indicated quercetin could act as a double-edged sword by strongly interacting with DENV envelope-glycoprotein (-8.1 kcal/mol) and NS5-RdRp domain (-8.0 kcal/mol), which are crucial for viral-attachment and replication. MD-simulation of docked complexes indicated their stability defined by low RMSD, RMSF, and stable H-bond with active-site residues. Significant reduction (p < 0.001) in TNF-α, IL-6, ROS-production, and vascular leakage was observed among pre-, co-, and post-treatment (24 and 48 HPI) groups with promising hepatic and renal-protective effects. Pharmacological and functional-molecular interaction networks indicate a significant effect of quercetin on vascular integrity byVEGF-KDR signaling pathway (via PI3K-Akt and Ras signalling), oxygen homeostasis through HIF-1 signalling, and the anti-inflammatory response via PI3K-Akt, IL-6 and its receptor signalling (PPI enrichment P = 3.19e-10).Thus, it can be concluded that I.P. co- and post-treatment (24hpi) of quercetin to DENV-infected mice could effectively reduce viral-titer, pro-inflammatory cytokines, ROS-response, and vascular permeability. Taken together this demonstrates quercetin as an important antiviral candidate against dengue.
目前,尚无临床批准的抗登革病毒(DENV)的抗病毒药物。本研究旨在通过分别经口服和腹腔内(I.P)途径对感染DENV的Balb/C小鼠进行预处理、联合治疗和感染后治疗(感染后24、48和72小时)来确定槲皮素的预防、抗病毒和治疗潜力。槲皮素的口服剂量为80mg/kg/天,腹腔内给药剂量为16mg/kg/天,均无毒性。发现腹腔内给药比口服给药更有效,腹腔内给药在联合治疗组(从第1天起,p<0.01)、感染后治疗组(感染后24小时)和预处理组(从第3天起,p<0.05)中显著降低了DENV拷贝数。分子对接实验表明,槲皮素可能是一把双刃剑,它与DENV包膜糖蛋白(-8.1kcal/mol)和NS5-RdRp结构域(-8.0kcal/mol)强烈相互作用,而这两个结构域对病毒附着和复制至关重要。对接复合物的分子动力学模拟表明它们的稳定性由低均方根偏差、均方根波动以及与活性位点残基的稳定氢键所定义。在预处理、联合治疗和感染后治疗(感染后24和48小时)组中观察到肿瘤坏死因子-α、白细胞介素-6、活性氧产生和血管渗漏显著降低(p<0.001),并具有良好的肝脏和肾脏保护作用。药理学和功能分子相互作用网络表明,槲皮素通过血管内皮生长因子-激酶插入结构域受体信号通路(通过磷脂酰肌醇-3-激酶-蛋白激酶B和Ras信号传导)对血管完整性、通过缺氧诱导因子-1信号传导对氧稳态以及通过磷脂酰肌醇-3-激酶-蛋白激酶B、白细胞介素-6及其受体信号传导(蛋白质-蛋白质相互作用富集P=3.19e-10)产生显著影响。因此,可以得出结论,对感染DENV的小鼠进行腹腔内联合治疗和感染后治疗(感染后24小时)可以有效降低病毒滴度、促炎细胞因子、活性氧反应和血管通透性。综上所述,这表明槲皮素是一种重要的抗登革病毒候选药物。