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10.1016/j.mehy.2020.110201

http://scihub22266oqcxt.onion/10.1016/j.mehy.2020.110201
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33017909!7430244!33017909
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suck abstract from ncbi

pmid33017909      Med+Hypotheses 2020 ; 143 (?): 110201
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  • Could aquaporin modulators be employed as prospective drugs for COVID-19 related pulmonary comorbidity? #MMPMID33017909
  • Mariajoseph-Antony LF; Kannan A; Panneerselvam A; Loganathan C; Anbarasu K; Prahalathan C
  • Med Hypotheses 2020[Oct]; 143 (?): 110201 PMID33017909show ga
  • COVID-19 initially an epidemic caused by SARS-CoV-2 has turned out to be a life- threatening global pandemic with increased morbidity and mortality. The presence of cytokine storm has been linked with the pathogenesis of severe lung injury as evinced in COVID-19. Aquaporins (AQPs) are molecular water channels, facilitating water transport across the cell membrane in response to osmotic gradients. Impairment in alveolar fluid clearance due to altered functional expression of respiratory AQPs highlight their pathophysiological significance in pulmonary edema associated respiratory illness. Therefore, we hypothesize that targeted modulation of AQPs in lungs in the intervening period of time, could diminish the dreadful effects of inflammation- induced comorbidity in COVID-19.
  • |Animals[MESH]
  • |Aquaporins/*metabolism[MESH]
  • |Betacoronavirus[MESH]
  • |Biological Transport[MESH]
  • |COVID-19[MESH]
  • |COVID-19 Drug Treatment[MESH]
  • |Comorbidity[MESH]
  • |Coronavirus Infections/*drug therapy[MESH]
  • |Cytokines/metabolism[MESH]
  • |Humans[MESH]
  • |Inflammation[MESH]
  • |Lung/immunology/virology[MESH]
  • |Mice[MESH]
  • |Pandemics[MESH]
  • |Pneumonia, Viral/*drug therapy[MESH]
  • |Pulmonary Edema/*drug therapy[MESH]


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