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Influence of Herbal Medicines on HMGB1 Release, SARS-CoV-2 Viral Attachment, Acute Respiratory Failure, and Sepsis. A Literature Review.
Wyganowska-Swiatkowska, Marzena; Nohawica, Michal; Grocholewicz, Katarzyna; Nowak, Gerard.
  • Wyganowska-Swiatkowska M; Chair of Department of Dental Surgery and Periodontology, Poznan University of Medicinal Sciences, Bukowska 70, 60-812 Poznan, Poland.
  • Nohawica M; Chair of Department of Dental Surgery and Periodontology, Poznan University of Medicinal Sciences, Bukowska 70, 60-812 Poznan, Poland.
  • Grocholewicz K; Department of Interdisciplinary Dentistry, Pomeranian Medical University, Al. Powstancow Wlkp. 72, 70-111 Szczecin, Poland.
  • Nowak G; Department of Medicinal and Cosmetic Natural Products, Poznan University of Medicinal Sciences, Mazowiecka 33, 60-623 Poznan, Poland.
Int J Mol Sci ; 21(13)2020 Jun 30.
Article in English | MEDLINE | ID: covidwho-635461
ABSTRACT
By attaching to the angiotensin converting enzyme 2 (ACE2) protein on lung and intestinal cells, Sudden Acute Respiratory Syndrome (SARS-CoV-2) can cause respiratory and homeostatic difficulties leading to sepsis. The progression from acute respiratory failure to sepsis has been correlated with the release of high-mobility group box 1 protein (HMGB1). Lack of effective conventional treatment of this septic state has spiked an interest in alternative medicine. This review of herbal extracts has identified multiple candidates which can target the release of HMGB1 and potentially reduce mortality by preventing progression from respiratory distress to sepsis. Some of the identified mixtures have also been shown to interfere with viral attachment. Due to the wide variability in chemical superstructure of the components of assorted herbal extracts, common motifs have been identified. Looking at the most active compounds in each extract it becomes evident that as a group, phenolic compounds have a broad enzyme inhibiting function. They have been shown to act against the priming of SARS-CoV-2 attachment proteins by host and viral enzymes, and the release of HMGB1 by host immune cells. An argument for the value in a nonspecific inhibitory action has been drawn. Hopefully these findings can drive future drug development and clinical procedures.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Respiratory Insufficiency / Sepsis / HMGB1 Protein / Betacoronavirus Type of study: Prognostic study / Reviews Topics: Traditional medicine Limits: Humans Language: English Year: 2020 Document Type: Article Affiliation country: Ijms21134639

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Respiratory Insufficiency / Sepsis / HMGB1 Protein / Betacoronavirus Type of study: Prognostic study / Reviews Topics: Traditional medicine Limits: Humans Language: English Year: 2020 Document Type: Article Affiliation country: Ijms21134639