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10.3390/ijms21114084

http://scihub22266oqcxt.onion/10.3390/ijms21114084
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32521619!7312898!32521619
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suck abstract from ncbi


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pmid32521619      Int+J+Mol+Sci 2020 ; 21 (11): ä
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  • Redox-Modulating Agents in the Treatment of Viral Infections #MMPMID32521619
  • Checconi P; De Angelis M; Marcocci ME; Fraternale A; Magnani M; Palamara AT; Nencioni L
  • Int J Mol Sci 2020[Jun]; 21 (11): ä PMID32521619show ga
  • Viruses use cell machinery to replicate their genome and produce viral proteins. For this reason, several intracellular factors, including the redox state, might directly or indirectly affect the progression and outcome of viral infection. In physiological conditions, the redox balance between oxidant and antioxidant species is maintained by enzymatic and non-enzymatic systems, and it finely regulates several cell functions. Different viruses break this equilibrium and induce an oxidative stress that in turn facilitates specific steps of the virus lifecycle and activates an inflammatory response. In this context, many studies highlighted the importance of redox-sensitive pathways as novel cell-based targets for therapies aimed at blocking both viral replication and virus-induced inflammation. In the review, we discuss the most recent findings in this field. In particular, we describe the effects of natural or synthetic redox-modulating molecules in inhibiting DNA or RNA virus replication as well as inflammatory pathways. The importance of the antioxidant transcription factor Nrf2 is also discussed. Most of the data reported here are on influenza virus infection. We believe that this approach could be usefully applied to fight other acute respiratory viral infections characterized by a strong inflammatory response, like COVID-19.
  • |Animals[MESH]
  • |Antiviral Agents/*therapeutic use[MESH]
  • |COVID-19 Drug Treatment[MESH]
  • |Coronavirus Infections/drug therapy[MESH]
  • |Glutathione/metabolism[MESH]
  • |Humans[MESH]
  • |Inflammation/drug therapy[MESH]
  • |Influenza, Human/drug therapy[MESH]
  • |Oxidation-Reduction/*drug effects[MESH]
  • |Virus Diseases/*drug therapy/immunology/pathology[MESH]


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