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10.1007/s11481-020-09979-8

http://scihub22266oqcxt.onion/10.1007/s11481-020-09979-8
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33426604!7797355!33426604
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suck abstract from ncbi


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pmid33426604      J+Neuroimmune+Pharmacol 2021 ; 16 (1): 59-70
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  • ACE-2-interacting Domain of SARS-CoV-2 (AIDS) Peptide Suppresses Inflammation to Reduce Fever and Protect Lungs and Heart in Mice: Implications for COVID-19 Therapy #MMPMID33426604
  • Paidi RK; Jana M; Mishra RK; Dutta D; Raha S; Pahan K
  • J Neuroimmune Pharmacol 2021[Mar]; 16 (1): 59-70 PMID33426604show ga
  • COVID-19 is an infectious respiratory illness caused by the virus strain severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and until now, there is no effective therapy against COVID-19. Since SARS-CoV-2 binds to angiotensin-converting enzyme 2 (ACE2) for entering into host cells, to target COVID-19 from therapeutic angle, we engineered a hexapeptide corresponding to the ACE2-interacting domain of SARS-CoV-2 (AIDS) that inhibits the association between receptor-binding domain-containing spike S1 and ACE-2. Accordingly, wild type (wt), but not mutated (m), AIDS peptide inhibited SARS-CoV-2 spike S1-induced activation of NF-kappaB and expression of IL-6 in human lungs cells. Interestingly, intranasal intoxication of C57/BL6 mice with recombinant SARS-CoV-2 spike S1 led to fever, increase in IL-6 in lungs, infiltration of neutrophils into the lungs, arrhythmias, and impairment in locomotor activities, mimicking some of the important symptoms of COVID-19. However, intranasal treatment with wtAIDS, but not mAIDS, peptide reduced fever, protected lungs, improved heart function, and enhanced locomotor activities in SARS-CoV-2 spike S1-intoxicated mice. Therefore, selective targeting of ACE2-to-SARS-CoV-2 interaction by wtAIDS may be beneficial for COVID-19.
  • |*COVID-19 Drug Treatment[MESH]
  • |Administration, Intranasal[MESH]
  • |Angiotensin-Converting Enzyme 2/*therapeutic use[MESH]
  • |Animals[MESH]
  • |Arrhythmias, Cardiac/etiology/prevention & control[MESH]
  • |COVID-19/*complications/pathology[MESH]
  • |Female[MESH]
  • |Fever/*drug therapy/*etiology[MESH]
  • |Heart Diseases/*etiology/pathology/*prevention & control[MESH]
  • |Inflammation/*drug therapy/*etiology[MESH]
  • |Interleukin-6/metabolism[MESH]
  • |Lung Diseases/*etiology/pathology/*prevention & control[MESH]
  • |Male[MESH]
  • |Mice[MESH]
  • |Mice, Inbred C57BL[MESH]
  • |Motor Activity/drug effects[MESH]
  • |Neutrophil Infiltration/drug effects[MESH]
  • |Peptide Fragments/*therapeutic use[MESH]


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