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10.1007/s00011-020-01422-1

http://scihub22266oqcxt.onion/10.1007/s00011-020-01422-1
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33206207!7673069!33206207
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suck abstract from ncbi

pmid33206207      Inflamm+Res 2021 ; 70 (1): 67-75
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  • Histamine receptors and COVID-19 #MMPMID33206207
  • Ennis M; Tiligada K
  • Inflamm Res 2021[Jan]; 70 (1): 67-75 PMID33206207show ga
  • OBJECTIVE: Reports that the over-the-counter histamine H(2) receptor antagonist famotidine could help treat the novel coronavirus disease (COVID-19) appeared from April 2020. We, therefore, examined reports on interactions between severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and histamine receptor antagonists. METHODS: A systematic literature search was performed by 19 September 2020, and updated on 28 October 2020, in PubMed, Scopus, Cochrane Library and Google Scholar using (COVID-19 OR coronavirus OR SARS-CoV-2) AND (histamine antagonist OR famotidine OR cimetidine). ClinicalTrials.gov was searched for COVID-19 and (famotidine or histamine). RESULTS: Famotidine may be a useful addition in COVID-19 treatment, but the results from prospective randomized trials are as yet awaited. Bioinformatics/drug repurposing studies indicated that, among several medicines, H(1) and H(2) receptor antagonists may interact with key viral enzymes. However, in vitro studies have to date failed to show a direct inhibition of famotidine on SARS-CoV-2 replication. CONCLUSIONS: Clinical research into the potential benefits of H(2) receptor antagonists in managing COVID-19 inflammation began from a simple observation and now is being tested in multi-centre clinical trials. The positive effects of famotidine may be due to H(2) receptor-mediated immunomodulatory actions on mast cell histamine-cytokine cross-talk, rather than a direct action on SARS-CoV-2.
  • |*COVID-19 Drug Treatment[MESH]
  • |COVID-19/metabolism[MESH]
  • |Histamine Antagonists/*therapeutic use[MESH]
  • |Histamine H2 Antagonists/therapeutic use[MESH]
  • |Humans[MESH]
  • |Receptors, Histamine/*drug effects/metabolism[MESH]


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