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10.1016/j.amjms.2020.07.018

http://scihub22266oqcxt.onion/10.1016/j.amjms.2020.07.018
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32736832!7362851!32736832
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suck abstract from ncbi


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pmid32736832      Am+J+Med+Sci 2020 ; 360 (4): 338-341
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  • Can a Combination of AT1R Antagonist and Vitamin D Treat the Lung Complication of COVID-19? #MMPMID32736832
  • Rafiullah M
  • Am J Med Sci 2020[Oct]; 360 (4): 338-341 PMID32736832show ga
  • Severe Acute Respiratory Distress Syndrome caused by a novel human coronavirus SARS-CoV-2 named COVID-19 and declared as a pandemic. This paper reviews the possibility of repurposing angiotensin type 1 receptor (AT1R) antagonists and vitamin D to treat COVID-19. ACE2 protein found on the cell membranes is the target of SARS-CoV-2 for entering into the host cells. Viral spike protein-binding with ACE2 down-regulates it. As ACE2 is known to protect the lung from injuries, SARS-CoV-2-induced ACE2 deficiency may expose patients to lung damage. AT1R antagonists and vitamin D increase the expression of ACE2 independently. Besides, vitamin D suppresses the compensatory increase in renin levels following the inhibition of the renin-angiotensin system by AT1R antagonists. Therefore, a combination of AT1R antagonists and vitamin D may offer protection against COVID-19 induced lung injury.
  • |Angiotensin II Type 1 Receptor Blockers/pharmacology/*therapeutic use[MESH]
  • |Angiotensin-Converting Enzyme 2[MESH]
  • |Animals[MESH]
  • |Betacoronavirus[MESH]
  • |COVID-19[MESH]
  • |COVID-19 Drug Treatment[MESH]
  • |Coronavirus Infections/blood/complications/*drug therapy[MESH]
  • |Host-Pathogen Interactions[MESH]
  • |Humans[MESH]
  • |Pandemics[MESH]
  • |Peptidyl-Dipeptidase A/blood[MESH]
  • |Pneumonia, Viral/blood/complications/*drug therapy[MESH]
  • |Renin-Angiotensin System/drug effects[MESH]
  • |SARS-CoV-2[MESH]
  • |Severe Acute Respiratory Syndrome/*drug therapy/virology[MESH]
  • |Virus Internalization[MESH]
  • |Vitamin D/pharmacology/*therapeutic use[MESH]


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