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10.1016/j.cbi.2021.109567

http://scihub22266oqcxt.onion/10.1016/j.cbi.2021.109567
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34166652!8217345!34166652
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suck abstract from ncbi

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  • TRP channels in COVID-19 disease: Potential targets for prevention and treatment #MMPMID34166652
  • Jaffal SM; Abbas MA
  • Chem Biol Interact 2021[Aug]; 345 (ä): 109567 PMID34166652show ga
  • Coronavirus disease 2019 [COVID-19] is a global health threat caused by severe acute respiratory syndrome coronavirus 2 [SARS-CoV2] that requires two proteins for entry: angiotensin-converting enzyme 2 [ACE2] and -membrane protease serine 2 [TMPRSS2]. Many patients complain from pneumonia, cough, fever, and gastrointestinal (GI) problems. Notably, different TRP channels are expressed in various tissues infected by SARS-CoV-2. TRP channels are cation channels that show a common architecture with high permeability to calcium [Ca(2+)] in most sub-families. Literature review shed light on the possible role of TRP channels in COVID-19 disease. TRP channels may take part in inflammation, pain, fever, anosmia, ageusia, respiratory, cardiovascular, GI and neurological complications related to COVID-19. Also, TRP channels could be the targets for many active compounds that showed effectiveness against SARS-CoV-2. Desensitization or blocking TRP channels by antibodies, aptamers, small molecules or venoms can be an option for COVID-19 prevention and future treatment. This review provides insights into the involvement of TRP channels in different symptoms and mechanisms of SARS-CoV-2 , potential treatments targeting these channels and highlights missing gaps in literature.
  • |*Molecular Targeted Therapy[MESH]
  • |COVID-19/*drug therapy/metabolism/*prevention & control[MESH]
  • |Humans[MESH]
  • |Transient Receptor Potential Channels/*metabolism[MESH]


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  • suck abstract from ncbi

    109567 ä.345 2021