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10.1016/j.peptides.2020.170428

http://scihub22266oqcxt.onion/10.1016/j.peptides.2020.170428
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suck abstract from ncbi


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pmid33065209      Peptides 2021 ; 135 (ä): 170428
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  • The role of kallikrein-kinin and renin-angiotensin systems in COVID-19 infection #MMPMID33065209
  • Carvalho PR; Sirois P; Fernandes PD
  • Peptides 2021[Jan]; 135 (ä): 170428 PMID33065209show ga
  • In November 2019 the first cases of a novel acute respiratory syndrome has been reported in Wuhan province, China. Soon after, in January 2020 the World Health Organization declared a pandemic state due to the dissemination of a virus named SARS-CoV-2 (severe acute respiratory syndrome coronavirus 2), the cause of coronavirus disease 2019 (COVID-19). Being an unknown disease, it is essential to assess not only its main characteristic features and overall clinical symptomatology but also its patient infection mode and propagation to design appropriate clinical interventions and treatments. In this review the pathophysiology of SARS-CoV-2 infection and how the virus enters the cells and activates the immune system are described. The role of three systems involved in the SARS- CoV-2 infection (renin-angiotensin, kinin and coagulation systems) is discussed with the objectives to identify and try to explain several of the events observed during the evolution of the disease and to suggest possible targets for therapeutic interventions.
  • |Animals[MESH]
  • |Antiviral Agents/pharmacology[MESH]
  • |COVID-19 Drug Treatment[MESH]
  • |COVID-19/immunology/metabolism/*physiopathology/transmission[MESH]
  • |Drug Repositioning[MESH]
  • |Host-Pathogen Interactions[MESH]
  • |Humans[MESH]
  • |Kallikreins/*metabolism[MESH]
  • |Kinins/*metabolism[MESH]
  • |Renin-Angiotensin System/*physiology[MESH]
  • |Renin/metabolism[MESH]
  • |SARS-CoV-2/genetics/*pathogenicity[MESH]


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