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Coronavirus disease 2019 (COVID-19), human erythrocytes and the PKC-alpha/-beta inhibitor chelerythrine –possible therapeutic implication

Mehrdad Ghashghaeinia, Peter Dreischer, Thomas Wieder, Martin Köberle

2020Cell Cycle21 citationsDOIOpen Access PDF

Abstract

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes COVID-19. Until now, diverse drugs have been used for the treatment of COVID-19. These drugs are associated with severe side effects, e.g. induction of erythrocyte death, named eryptosis. This massively affects the oxygen (O2) supply of the organism. Therefore, three elementary aspects should be considered simultaneously: (1) a potential drug should directly attack the virus, (2) eliminate virus-infected host cells and (3) preserve erythrocyte survival and functionality. It is known that PKC-α inhibition enhances the vitality of human erythrocytes, while it dose-dependently activates the apoptosis machinery in nucleated cells. Thus, the use of chelerythrine as a specific PKC-alpha and -beta (PKC-α/-β) inhibitor should be a promising approach to treat people infected with SARS-CoV-2.

Topics & Concepts

ChelerythrineProtein kinase CCoronavirusApoptosisAlpha (finance)VirusCoronavirus disease 2019 (COVID-19)Programmed cell deathDrugPharmacologyVirologySevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2)BETA (programming language)BiologyMedicineChemistryDiseaseImmunologyCancer researchCell biologySignal transductionBiochemistryInternal medicineInfectious disease (medical specialty)Construct validityComputer scienceNursingPatient satisfactionProgramming languageErythrocyte Function and PathophysiologyCalcium signaling and nucleotide metabolismPancreatic function and diabetes
Coronavirus disease 2019 (COVID-19), human erythrocytes and the PKC-alpha/-beta inhibitor chelerythrine –possible therapeutic implication | Litcius