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May 4, 2026Pharmaceuticals0 citationsOpen Access

Integrated Evaluation of Urtica dioica Extract Assessing Physiochemical Analysis with Antioxidant, Antiviral, and Immunomodulatory Effects Against SARS-CoV-2

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GAGülşah AkbaşŞAŞeyma AydınlıkJDJenya Dursun

Key Points

  • This study aims to evaluate the antioxidant, antiviral, and immunomodulatory effects of Urtica dioica extract against SARS-CoV-2.
  • Evaluated the physicochemical properties of Urtica dioica extract using microtiter assays and HPLC analysis.
  • Assessed cytocompatibility in HEK293T, Vero E6, Caco-2, and Calu-3 cell lines.
  • Conducted ELISA and FRET assays to measure inhibition of SARS-CoV-2 receptor and main protease activity.
  • UdE at 100 µg/mL inhibited RBD–ACE2 binding by 94%.
  • Suppressed Mpro activity by 74% and showed 33.6% inhibition of pseudovirus entry at 300 µg/mL.
  • Significantly suppressed IL-1β and IL-6 production while increasing TNF-α and IL-8 levels.

Abstract

Background: A major challenge in antiviral development is the identification of novel virus–host interactions while ensuring therapeutic efficacy and safety. These challenges have renewed interest in phytochemicals derived from medicinal plants as alternative antiviral agents. Objectives: In this study, we investigated the antioxidant, antiviral, and immunomodulatory properties of a Mediterranean Urtica dioica extract (UdE) against SARS-CoV-2 using chemical, biochemical, and in vitro approaches. Methods: The physicochemical properties of UdE were characterized using microtiter assays and HPLC analysis. Cytocompatibility was evaluated in HEK293T, Vero E6, Caco-2, and Calu-3 cell lines while antioxidant activity was assessed using both chemical and cell-based assays. Antiviral activity was evaluated by assessing inhibition of SARS-CoV-2 receptor binding domain (RBD)–ACE2 interaction using ELISA, inhibition of SARS-CoV-2 main protease (Mpro) activity via FRET assay and inhibition of viral entry using SARS-CoV-2 S1 pseudovirus neutralization assay. Results: UdE (100 µg/mL) inhibited RBD–ACE2 binding by 94% and suppressed Mpro activity by 74%, while reducing moderate but significant inhibition of pseudovirus entry (33.6%) at 300 µg/mL dose level in ACE2 expressing HEK293T cells. Immunomodulatory analysis revealed significant suppression of IL-1β and IL-6 production, accompanied by increased TNF-α and IL-8 levels. Conclusions: Collectively, these findings highlight that UdE exhibits multi-target in vitro antioxidant, antiviral, and immunomodulatory activity against SARS-CoV-2; therefore, UdE represents a promising bioactive extract for the management of SARS-CoV-2 infection.

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Cite This Study

Akbaş et al. (2026) studied this question.

synapsesocial.com/papers/69f836d93ed186a739980f80https://doi.org/10.3390/ph19050693
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