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10.1016/j.heliyon.2020.e04900

http://scihub22266oqcxt.onion/10.1016/j.heliyon.2020.e04900
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suck abstract from ncbi


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pmid32935064      Heliyon 2020 ; 6 (9): e04900
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  • Chloroquine to fight COVID-19: A consideration of mechanisms and adverse effects? #MMPMID32935064
  • Zhan X; Dowell S; Shen Y; Lee DL
  • Heliyon 2020[Sep]; 6 (9): e04900 PMID32935064show ga
  • The COVID-19 outbreak emerged in December 2019 and has rapidly become a global pandemic. A great deal of effort has been made to find effective drugs against this disease. Chloroquine (CQ) and hydroxychloroquine (HCQ) were widely adopted in treating COVID-19, but the results were contradictive. CQ/HCQ have been used to prevent and treat malaria and are efficacious anti-inflammatory agents in rheumatoid arthritis and systemic lupus erythematosus. These drugs have potential broad-spectrum antiviral properties, but the underlying mechanisms are speculative. In this review, we re-evaluated the treatment outcomes and current hypothesis for the working mechanisms of CQ/HCQ as COVID-19 therapy with a special focus on disruption of Ca(2+) signaling. In so doing, we attempt to show how the different hypotheses for CQ/HCQ action on coronavirus may interact and reinforce each other. The potential toxicity is also noted due to its action on Ca(2+) and hyperpolarization-activated cyclic nucleotide-gated channels in cardiac myocytes and neuronal cells. We propose that intracellular calcium homeostasis is an alternative mechanism for CQ/HCQ pharmacology, which should be considered when evaluating the risks and benefits of therapy in these patients and other perspective applications.
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