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COVID-19 Calls for Mathematics, Part 2: Interleukin IL-6 and Myo-Inositol, Suicide-substrate Enzyme Inhibitors

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  • Additional Information
    • Contributors:
      Dipartimento di Matematica = Istituto Matematico "Guido Castelnuovo" La Sapienza, Rome; Università degli Studi di Roma "La Sapienza" = Sapienza University Rome (UNIROMA); Laboratoire Jean Alexandre Dieudonné (LJAD); Université Nice Sophia Antipolis (1965 - 2019) (UNS)-Centre National de la Recherche Scientifique (CNRS)-Université Côte d'Azur (UniCA); This project is partially supported by the French government, managed by the ANR under the UCA JEDI Investments for the Future project (reference No. ANR-15-IDEX-01); ANR-15-IDEX-0001,UCA JEDI,Idex UCA JEDI(2015)
    • Publication Information:
      CCSD
      Sapienza University of Rome
    • Publication Date:
      2020
    • Collection:
      HAL Université Côte d'Azur
    • Abstract:
      International audience ; Interleukin IL-6 is a cytokine produced in response to various types of damage (infections, tissue injuries, autoimmune diseases, etc.) whose action contributes to host defense through stimulation of acute phase responses and immune reactions. However, experimental data show that high concentration levels of interleukin IL-6, and the subsequent inflammatory cascade induced into the organisms, could lead to several complications, such as organs progressive deterioration. The abnormal release of interleukin IL-6 is also a consequence of SARS-CoV-2 virus contagion, usually causing interstitial pneumonia and respiratory failure, which appear to be the source of decease in most of patients. Tocilizumab and myo-Inositol are two possible remedies proposed in the clinical literature to contrast the uncontrolled synthesis of interleukin IL-6, although the former exhibits non negligible collateral effects, differently from the latter. For this reason, the mathematical investigation of myo-Inositol interaction with other relevant substances involved in the SARS-CoV-2 could support the bio-medical research in determining, the optimal doses and administration timing necessary to minimize damages, in order to support the clinical results. The preliminaries of this approach are the subject of this article. Moreover, because a vaccine against the SARS-CoV-2 virus will not be available shortly, we consider another possible pharmacological strategy to contrast its activity. There exist several candidate medicines which may inhibit infection and replication of SARS-CoV-2, and we focus our attention on the process of enzymatic inhibition through mechanism-based enzyme inactivators. The so-called suicide-substrate strategies constitute a fascinating area of interdisciplinary research. We explain the procedure to represent mathematically how a hypothetical drug would act to inhibit the essential enzymes used by the SARS-CoV-2 virus to replicate and spread. Considering the biological aspects and the ...
    • Accession Number:
      10.13133/2532-5876/16969
    • Online Access:
      https://hal.science/hal-03032440
      https://hal.science/hal-03032440v1/document
      https://hal.science/hal-03032440v1/file/covid_math2_2020.pdf
      https://doi.org/10.13133/2532-5876/16969
    • Rights:
      https://about.hal.science/hal-authorisation-v1/ ; info:eu-repo/semantics/OpenAccess
    • Accession Number:
      edsbas.DD7D5834