Chittasupho Chuda, Srisawad Kamonwan, Arjsri Punnida, Phongpradist Rungsinee, Tingya Wipawan, Ampasavate Chadarat, Dejkriengkraikul Pornngarm
Department of Pharmaceutical Sciences, Faculty of Pharmacy, Chiang Mai University, Chiang Mai 50200, Thailand.
Department of Biochemistry, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.
Pharmaceuticals (Basel). 2023 Jun 9;16(6):862. doi: 10.3390/ph16060862.
Chronic inflammation and tissue damage can result from uncontrolled inflammation during SARS-CoV-2 or COVID-19 infections, leading to post-acute COVID conditions or long COVID. Curcumin, found in turmeric, has potent anti-inflammatory properties but limited effectiveness. This study developed nanocurcumin, a curcumin nanoparticle, to enhance its physical and chemical stability and investigate its in vitro anti-inflammatory properties upon CoV2-SP induction in lung epithelial cells. Nanocurcumin was prepared by encapsulating curcumin extract in phospholipids. The particle size, polydispersity index, and zeta potential of nanocurcumin were measured using dynamic light scattering. The encapsulated curcumin content was determined using HPLC analysis. The encapsulation efficiency of curcumin was 90.74 ± 5.35% as determined by HPLC. Regarding the in vitro release of curcumin, nanocurcumin displayed a higher release content than non-nanoparticle curcumin. Nanocurcumin was further investigated for its anti-inflammatory properties using A549 lung epithelial cell line. As determined by ELISA, nanocurcumin showed inhibitory effects on inflammatory cytokine releases in CoV2-SP-stimulated conditions, as evidenced by a significant decrease in IL-6, IL-1β and IL-18 cytokine secretions compared with the spike-stimulated control group ( < 0.05). Additionally, as determined by RT-PCR, nanocurcumin significantly inhibited the CoV2-SP-stimulated expression of inflammatory genes (, , , and ) compared with the spike-stimulated control group ( < 0.05). Regarding the inhibition of NLRP3 inflammasome machinery proteins by Western blot, nanocurcumin decreased the expressions of inflammasome machinery proteins including NLRP3, ASC, pro-caspase-1, and the active form of caspase-1 in CoV2-SP-stimulated A549 cells compared with the spike-stimulated control group ( < 0.05). Overall, the nanoparticle formulation of curcumin improved its solubility and bioavailability, demonstrating anti-inflammatory effects in a CoV2-SP-induced scenario by inhibiting inflammatory mediators and the NLRP3 inflammasome machinery. Nanocurcumin shows promise as an anti-inflammatory product for preventing COVID-19-related airway inflammation.
在严重急性呼吸综合征冠状病毒2(SARS-CoV-2)或冠状病毒病2019(COVID-19)感染期间,不受控制的炎症可导致慢性炎症和组织损伤,进而引发急性后新冠症状或长期新冠症状。姜黄素存在于姜黄中,具有强大的抗炎特性,但效果有限。本研究开发了纳米姜黄素,即姜黄素纳米颗粒,以增强其物理和化学稳定性,并研究其在肺上皮细胞中由新冠病毒刺突蛋白(CoV2-SP)诱导后的体外抗炎特性。纳米姜黄素是通过将姜黄素提取物包裹在磷脂中制备而成。使用动态光散射法测量纳米姜黄素的粒径、多分散指数和zeta电位。使用高效液相色谱(HPLC)分析测定包裹的姜黄素含量。通过HPLC测定,姜黄素的包封率为90.74±5.35%。关于姜黄素的体外释放,纳米姜黄素的释放量高于非纳米颗粒姜黄素。使用A549肺上皮细胞系进一步研究纳米姜黄素的抗炎特性。通过酶联免疫吸附测定(ELISA)确定,纳米姜黄素在CoV2-SP刺激条件下对炎性细胞因子释放具有抑制作用,与刺突蛋白刺激的对照组相比,白细胞介素-6(IL-6)、白细胞介素-1β(IL-1β)和白细胞介素-18(IL-18)细胞因子分泌显著减少(P<0.05)证明了这一点。此外,通过逆转录聚合酶链反应(RT-PCR)确定,与刺突蛋白刺激的对照组相比,纳米姜黄素显著抑制CoV2-SP刺激的炎症基因(IL-6、IL-1β、IL-18和TNF-α)的表达(P<0.05)。关于通过蛋白质免疫印迹法对NLRP3炎性小体机制蛋白的抑制作用,与刺突蛋白刺激的对照组相比,纳米姜黄素降低了CoV2-SP刺激的A549细胞中炎性小体机制蛋白的表达,包括NLRP3、凋亡相关斑点样蛋白(ASC)、前半胱天冬酶-1和活性形式的半胱天冬酶-1(P<0.05)。总体而言,姜黄素的纳米颗粒制剂提高了其溶解度和生物利用度,通过抑制炎症介质和NLRP3炎性小体机制,在CoV2-SP诱导的情况下显示出抗炎作用。纳米姜黄素有望成为预防COVID-19相关气道炎症的抗炎产品。