1
views
0
recommends
+1 Recommend
1 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Egyptian perspectives on potential risk of paracetamol/acetaminophen-induced toxicities: Lessons learnt during COVID-19 pandemic

      research-article
      a , * , 1 , b , a
      Toxicology Reports
      The Author(s). Published by Elsevier B.V.
      ALF, acute liver failure, CFA, confirmatory factor analysis, COVID-19, Coronavirus disease 2019, FDA, Food and Drug Administration, MERS-CoV, Middle East respiratory syndrome coronavirus, NSAIDs, non-steroidal anti-inflammatory drugs, OTC, over the counter, PHC, primary health care, ROS, reactive oxygen species, REC, Research Ethics committee, SARS-CoV, severe acute respiratory syndrome coronavirus, SARS-CoV-2, severe acute respiratory syndrome coronavirus 2, SD, standard deviation, WHO, World Health Organization, Acetaminophen, Paracetamol, Toxicity, Safe use, COVID-19, Egyptians

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Paracetamol/Acetaminophen was widely used as a first-line antipyretic and analgesic for COVID-19 patients without giving any attention to the potential risk of related toxicities. A survey was conducted on 176 Egyptians using an online survey portal to assess their knowledge, and attitude regarding potential risk of paracetamol toxicities and whether COVID-19 pandemic affected their practices regarding safe use of paracetamol. The self-administered questionnaire was developed by the researchers and was validated by expert opinions. A pilot testing of the questionnaire was done. Alpha Cronbach test used to assess the internal consistency reliability of the survey revealed good reliability. Overall percent-score revealed that only 24.4% of participants had good knowledge about paracetamol and its related potential toxicities. 62.5% of participants considered paracetamol safer than other medications of the same indications. 42.6% of participants could advise others to use paracetamol without prescription. According to the participants' responses, physicians were less concerned to give instructions about possibility of overdosage. Our results also revealed that participants’ administration of paracetamol without physician prescription was more during COVID-19. Practice of paracetamol administration more than the allowed number of tablets/day was significantly more evident during the pandemic. We concluded that the unsupervised use of paracetamol is an alarming sign that should be addressed as this could lead to a high rate of accidental paracetamol toxicity. A lesson learnt from COVID-19 pandemic is the need to implement behavior change measures to mitigate the risk of accidental paracetamol toxicity.

          Graphical Abstract

          Related collections

          Most cited references54

          • Record: found
          • Abstract: found
          • Article: not found

          Angiotensin-converting enzyme 2 is a functional receptor for the SARS coronavirus

          Spike (S) proteins of coronaviruses, including the coronavirus that causes severe acute respiratory syndrome (SARS), associate with cellular receptors to mediate infection of their target cells 1,2 . Here we identify a metallopeptidase, angiotensin-converting enzyme 2 (ACE2) 3,4 , isolated from SARS coronavirus (SARS-CoV)-permissive Vero E6 cells, that efficiently binds the S1 domain of the SARS-CoV S protein. We found that a soluble form of ACE2, but not of the related enzyme ACE1, blocked association of the S1 domain with Vero E6 cells. 293T cells transfected with ACE2, but not those transfected with human immunodeficiency virus-1 receptors, formed multinucleated syncytia with cells expressing S protein. Furthermore, SARS-CoV replicated efficiently on ACE2-transfected but not mock-transfected 293T cells. Finally, anti-ACE2 but not anti-ACE1 antibody blocked viral replication on Vero E6 cells. Together our data indicate that ACE2 is a functional receptor for SARS-CoV. Supplementary information The online version of this article (doi:10.1038/nature02145) contains supplementary material, which is available to authorized users.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Origin and evolution of pathogenic coronaviruses

            Severe acute respiratory syndrome coronavirus (SARS-CoV) and Middle East respiratory syndrome coronavirus (MERS-CoV) are two highly transmissible and pathogenic viruses that emerged in humans at the beginning of the 21st century. Both viruses likely originated in bats, and genetically diverse coronaviruses that are related to SARS-CoV and MERS-CoV were discovered in bats worldwide. In this Review, we summarize the current knowledge on the origin and evolution of these two pathogenic coronaviruses and discuss their receptor usage; we also highlight the diversity and potential of spillover of bat-borne coronaviruses, as evidenced by the recent spillover of swine acute diarrhoea syndrome coronavirus (SADS-CoV) to pigs.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: found
              Is Open Access

              Role of angiotensin-converting enzyme 2 (ACE2) in COVID-19

              Abstract An outbreak of pneumonia caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) that started in Wuhan, China, at the end of 2019 has become a global pandemic. Both SARS-CoV-2 and SARS-CoV enter host cells via the angiotensin-converting enzyme 2 (ACE2) receptor, which is expressed in various human organs. We have reviewed previously published studies on SARS and recent studies on SARS-CoV-2 infection, named coronavirus disease 2019 (COVID-19) by the World Health Organization (WHO), confirming that many other organs besides the lungs are vulnerable to the virus. ACE2 catalyzes angiotensin II conversion to angiotensin-(1–7), and the ACE2/angiotensin-(1–7)/MAS axis counteracts the negative effects of the renin-angiotensin system (RAS), which plays important roles in maintaining the physiological and pathophysiological balance of the body. In addition to the direct viral effects and inflammatory and immune factors associated with COVID-19 pathogenesis, ACE2 downregulation and the imbalance between the RAS and ACE2/angiotensin-(1–7)/MAS after infection may also contribute to multiple organ injury in COVID-19. The SARS-CoV-2 spike glycoprotein, which binds to ACE2, is a potential target for developing specific drugs, antibodies, and vaccines. Restoring the balance between the RAS and ACE2/angiotensin-(1–7)/MAS may help attenuate organ injuries. Graphical abstract SARS-CoV-2 enters lung cells via the ACE2 receptor. The cell-free and macrophage-phagocytosed virus can spread to other organs and infect ACE2-expressing cells at local sites, causing multi-organ injury.
                Bookmark

                Author and article information

                Journal
                Toxicol Rep
                Toxicol Rep
                Toxicology Reports
                The Author(s). Published by Elsevier B.V.
                2214-7500
                29 March 2022
                2022
                29 March 2022
                : 9
                : 541-548
                Affiliations
                [a ]Forensic Medicine and Clinical Toxicology Department, Faculty of Medicine, Suez Canal University, Ismailia, Egypt
                [b ]Public Health and Community Medicine Department, Faculty of Medicine, Port-Said University, Port-Said, Egypt
                Author notes
                [* ]Correspondence to: Faculty of Medicine, Suez Canal University, Ring Road, P.O. Box: 41522, Ismailia, Egypt.
                Article
                S2214-7500(22)00064-6
                10.1016/j.toxrep.2022.03.035
                8961937
                35371923
                aa495524-1b6f-41e6-8175-8dd3a049818d
                © 2022 The Authors

                Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.

                History
                : 1 October 2021
                : 4 January 2022
                : 26 March 2022
                Categories
                Article

                alf, acute liver failure,cfa, confirmatory factor analysis,covid-19, coronavirus disease 2019,fda, food and drug administration,mers-cov, middle east respiratory syndrome coronavirus,nsaids, non-steroidal anti-inflammatory drugs,otc, over the counter,phc, primary health care,ros, reactive oxygen species,rec, research ethics committee,sars-cov, severe acute respiratory syndrome coronavirus,sars-cov-2, severe acute respiratory syndrome coronavirus 2,sd, standard deviation,who, world health organization,acetaminophen,paracetamol,toxicity,safe use,covid-19,egyptians

                Comments

                Comment on this article