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10.1016/j.drudis.2021.02.010

http://scihub22266oqcxt.onion/10.1016/j.drudis.2021.02.010
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suck abstract from ncbi


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pmid33609783      Drug+Discov+Today 2021 ; 26 (5): 1311-1318
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  • Developing new drugs that activate the protective arm of the renin-angiotensin system as a potential treatment for respiratory failure in COVID-19 patients #MMPMID33609783
  • Latil M; Camelo S; Veillet S; Lafont R; Dilda PJ
  • Drug Discov Today 2021[May]; 26 (5): 1311-1318 PMID33609783show ga
  • COVID-19, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has reached pandemic proportions with negative impacts on global health, the world economy and human society. The clinical picture of COVID-19, and the fact that Angiotensin converting enzyme 2 (ACE2) is a receptor of SARS-CoV-2, suggests that SARS-CoV-2 infection induces an imbalance in the renin-angiotensin system (RAS). We review clinical strategies that are attempting to rebalance the RAS in COVID-19 patients by using ACE inhibitors, angiotensin receptor blockers, or agonists of angiotensin-II receptor type 2 or Mas receptor (MasR). We also propose that the new MasR activator BIO101, a pharmaceutical grade formulation of 20-hydroxyecdysone that has anti-inflammatory, anti-fibrotic and cardioprotective properties, could restore RAS balance and improve the health of COVID-19 patients who have severe pneumonia.
  • |*COVID-19 Drug Treatment[MESH]
  • |Angiotensin Receptor Antagonists/therapeutic use[MESH]
  • |Angiotensin-Converting Enzyme Inhibitors/therapeutic use[MESH]
  • |Animals[MESH]
  • |COVID-19/metabolism/virology[MESH]
  • |Commelinaceae[MESH]
  • |Drug Development[MESH]
  • |Ecdysone/analogs & derivatives/therapeutic use[MESH]
  • |Host-Pathogen Interactions[MESH]
  • |Humans[MESH]
  • |Plant Extracts/therapeutic use[MESH]
  • |Proto-Oncogene Mas[MESH]
  • |Proto-Oncogene Proteins/agonists/metabolism[MESH]
  • |Receptors, G-Protein-Coupled/agonists/metabolism[MESH]
  • |Renin-Angiotensin System/*drug effects[MESH]


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