Ultradiluted Eupatorium perfoliatum Prevents and Alleviates SARS-CoV-2 Spike Protein-Induced Lung Pathogenesis by Regulating Inflammatory Response and Apoptosis.

IF 2.9 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Anirban Roy, Avipsha Sarkar, Asit Kumar Roy, Tanusree Ghorai, Debadatta Nayak, Subhash Kaushik, Satadal Das
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引用次数: 0

Abstract

Background/objectives: SARS-CoV-2 provokes acute oxidative stress in the lungs via cytokines, inflammatory mediators, and apoptotic factors, which might cause alveolar injury followed by severe respiratory syndrome during COVID-19 infection. The lack of particular antivirals for SARS-CoV-2 has opened novel avenues of complementary and alternative medicine as a potential remedy. The current study explored the mechanistic role of the ultradiluted formulation of Eupatorium (UDE) against SARS-CoV-2 recombinant S protein-mediated oxidative stress and mitochondriopathy.

Methods: Cell line and BALB/c mice were used to report that SARS-CoV-2 S protein caused an inflammatory response and subsequent cytokine storm via the NF-κB pathway in the lung along with oxidative damage. Morphological examination was performed using DAPI staining and histology for treated cells and lung tissues of animals, respectively. The molecular mechanism of action of UDE was investigated through qRT-PCR for the genetic expressions of various cytokines, inflammatory, and apoptotic mediators; ELISA, immunofluorescence, immunohistochemistry, and Western blot for the translational expression of the same molecules assayed for genetic expressions; and biochemical assays for various enzymes and ROS.

Results: UDE treatment suppressed the inflammatory cell infiltration and tissue-level oxidative stress and safeguarded mitochondrial integrity from free radical-mediated oxidative damage. Additionally, UDE played a direct role in restoring cellular redox homeostasis and reducing the inflammatory response by suppressing NF-κB, IL-1β, IL-18, caspase-1 expression, and ROS formation. Further, a plausible mechanism of action of UDE against S protein-induced damage was proposed.

Conclusions: This study described a novel therapeutic approach against S protein-mediated hyperinflammation, apoptosis, and oxidative damage. Hence, UDE may be considered as a prospective alternative to combat life-threatening consequences of SARS-CoV-2 infection.

背景/目的:SARS-CoV-2 通过细胞因子、炎症介质和细胞凋亡因子在肺部引发急性氧化应激,可能导致肺泡损伤,继而在 COVID-19 感染期间引发严重的呼吸综合征。由于缺乏针对 SARS-CoV-2 的特效抗病毒药物,这为补充和替代医学提供了新的潜在治疗途径。本研究探讨了大戟超稀释制剂(UDE)对 SARS-CoV-2 重组 S 蛋白介导的氧化应激和线粒体病变的机理作用:方法:使用细胞系和 BALB/c 小鼠报道了 SARS-CoV-2 S 蛋白通过 NF-κB 通路在肺部引起炎症反应和随后的细胞因子风暴以及氧化损伤。对处理过的细胞和动物肺组织分别采用 DAPI 染色和组织学方法进行了形态学检查。通过 qRT-PCR 检测各种细胞因子、炎症和凋亡介质的基因表达;ELISA、免疫荧光、免疫组织化学和 Western 印迹检测基因表达检测的相同分子的翻译表达;以及各种酶和 ROS 的生化检测,研究了 UDE 的分子作用机制:结果:UDE 治疗抑制了炎症细胞浸润和组织水平的氧化应激,保护了线粒体完整性免受自由基介导的氧化损伤。此外,UDE 通过抑制 NF-κB、IL-1β、IL-18、caspase-1 的表达和 ROS 的形成,在恢复细胞氧化还原平衡和减轻炎症反应方面发挥了直接作用。此外,还提出了 UDE 对抗 S 蛋白诱导的损伤的合理作用机制:本研究描述了一种针对 S 蛋白介导的过度炎症、细胞凋亡和氧化损伤的新型治疗方法。因此,UDE 可被视为对抗 SARS-CoV-2 感染危及生命后果的一种前瞻性替代疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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