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suck abstract from ncbi


10.1007/s12975-020-00818-9

http://scihub22266oqcxt.onion/10.1007/s12975-020-00818-9
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32378030!7202903!32378030
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suck abstract from ncbi

pmid32378030      Transl+Stroke+Res 2020 ; 11 (3): 322-325
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  • COVID-19-Related Stroke #MMPMID32378030
  • Hess DC; Eldahshan W; Rutkowski E
  • Transl Stroke Res 2020[Jun]; 11 (3): 322-325 PMID32378030show ga
  • The COVID-19 pandemic is associated with neurological symptoms and complications including stroke. There is hypercoagulability associated with COVID-19 that is likely a "sepsis-induced coagulopathy" and may predispose to stroke. The SARS-CoV-2 virus binds to angiotensin-converting enzyme 2 (ACE2) present on brain endothelial and smooth muscle cells. ACE2 is a key part of the renin angiotensin system (RAS) and a counterbalance to angiotensin-converting enzyme 1 (ACE1) and angiotensin II. Angiotensin II is proinflammatory, is vasoconstrictive, and promotes organ damage. Depletion of ACE2 by SARS-CoV-2 may tip the balance in favor of the "harmful" ACE1/angiotensin II axis and promote tissue injury including stroke. There is a rationale to continue to treat with tissue plasminogen activator for COVID-19-related stroke and low molecular weight heparinoids may reduce thrombosis and mortality in sepsis-induced coagulopathy.
  • |Angiotensin-Converting Enzyme 2[MESH]
  • |Betacoronavirus/metabolism[MESH]
  • |COVID-19[MESH]
  • |Coronavirus Infections/blood/*complications/drug therapy/epidemiology[MESH]
  • |Disseminated Intravascular Coagulation/drug therapy/virology[MESH]
  • |Female[MESH]
  • |Humans[MESH]
  • |Male[MESH]
  • |Pandemics[MESH]
  • |Peptidyl-Dipeptidase A/administration & dosage/metabolism[MESH]
  • |Pneumonia, Viral/blood/*complications/drug therapy/epidemiology[MESH]
  • |Recombinant Proteins/administration & dosage[MESH]
  • |SARS-CoV-2[MESH]
  • |Stroke/drug therapy/*virology[MESH]


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