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Silent hypoxia: higher NO in red blood cells of COVID-19 patients

BACKGROUND: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) that causes coronavirus disease 2019 (COVID-19) has spread to almost 100 countries, infected over 31 M patients and resulted in 961 K deaths worldwide as of 21st September 2020. The major clinical feature of severe COVID-19 req...

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Autores principales: Mortaz, Esmaeil, Malkmohammad, Majid, Jamaati, Hamidreza, Naghan, Parisa Adimi, Hashemian, Seyed MohamadReza, Tabarsi, Payam, Varahram, Maohammad, Zaheri, Hamidreza, Chousein, Efsun Gonca Uğur, Folkerts, Gert, Adcock, Ian M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7563910/
https://www.ncbi.nlm.nih.gov/pubmed/33066765
http://dx.doi.org/10.1186/s12890-020-01310-8
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author Mortaz, Esmaeil
Malkmohammad, Majid
Jamaati, Hamidreza
Naghan, Parisa Adimi
Hashemian, Seyed MohamadReza
Tabarsi, Payam
Varahram, Maohammad
Zaheri, Hamidreza
Chousein, Efsun Gonca Uğur
Folkerts, Gert
Adcock, Ian M.
author_facet Mortaz, Esmaeil
Malkmohammad, Majid
Jamaati, Hamidreza
Naghan, Parisa Adimi
Hashemian, Seyed MohamadReza
Tabarsi, Payam
Varahram, Maohammad
Zaheri, Hamidreza
Chousein, Efsun Gonca Uğur
Folkerts, Gert
Adcock, Ian M.
author_sort Mortaz, Esmaeil
collection PubMed
description BACKGROUND: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) that causes coronavirus disease 2019 (COVID-19) has spread to almost 100 countries, infected over 31 M patients and resulted in 961 K deaths worldwide as of 21st September 2020. The major clinical feature of severe COVID-19 requiring ventilation is acute respiratory distress syndrome (ARDS) with multi-functional failure as a result of a cytokine storm with increased serum levels of cytokines. The pathogenesis of the respiratory failure in COVID-19 is yet unknown, but diffuse alveolar damage with interstitial thickening leading to compromised gas exchange is a plausible mechanism. Hypoxia is seen in the COVID-19 patients, however, patients present with a distinct phenotype. Intracellular levels of nitric oxide (NO) play an important role in the vasodilation of small vessels. To elucidate the intracellular levels of NO inside of RBCs in COVID-19 patients compared with that of healthy control subjects. METHODS: We recruited 14 COVID-19 infected cases who had pulmonary involvement of their disease, 4 non-COVID-19 healthy controls (without pulmonary involvement and were not hypoxic) and 2 hypoxic non-COVID-19 patients subjects who presented at the Masih Daneshvari Hospital of Tehran, Iran between March–May 2020. Whole blood samples were harvested from patients and intracellular NO levels in 1 × 10(6) red blood cells (RBC) was measured by DAF staining using flow cytometry (FACS Calibour, BD, CA, USA). RESULTS: The Mean florescent of intensity for NO was significantly enhanced in COVID-19 patients compared with healthy control subjects (P ≤ 0.05). As a further control for whether hypoxia induced this higher intracellular NO, we evaluated the levels of NO inside RBC of hypoxic patients. No significant differences in NO levels were seen between the hypoxic and non-hypoxic control group. CONCLUSIONS: This pilot study demonstrates increased levels of intracellular NO in RBCs from COVID-19 patients. Future multi-centre studies should examine whether this is seen in a larger number of COVID-19 patients and whether NO therapy may be of use in these severe COVID-19 patients.
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spelling pubmed-75639102020-10-16 Silent hypoxia: higher NO in red blood cells of COVID-19 patients Mortaz, Esmaeil Malkmohammad, Majid Jamaati, Hamidreza Naghan, Parisa Adimi Hashemian, Seyed MohamadReza Tabarsi, Payam Varahram, Maohammad Zaheri, Hamidreza Chousein, Efsun Gonca Uğur Folkerts, Gert Adcock, Ian M. BMC Pulm Med Research Article BACKGROUND: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) that causes coronavirus disease 2019 (COVID-19) has spread to almost 100 countries, infected over 31 M patients and resulted in 961 K deaths worldwide as of 21st September 2020. The major clinical feature of severe COVID-19 requiring ventilation is acute respiratory distress syndrome (ARDS) with multi-functional failure as a result of a cytokine storm with increased serum levels of cytokines. The pathogenesis of the respiratory failure in COVID-19 is yet unknown, but diffuse alveolar damage with interstitial thickening leading to compromised gas exchange is a plausible mechanism. Hypoxia is seen in the COVID-19 patients, however, patients present with a distinct phenotype. Intracellular levels of nitric oxide (NO) play an important role in the vasodilation of small vessels. To elucidate the intracellular levels of NO inside of RBCs in COVID-19 patients compared with that of healthy control subjects. METHODS: We recruited 14 COVID-19 infected cases who had pulmonary involvement of their disease, 4 non-COVID-19 healthy controls (without pulmonary involvement and were not hypoxic) and 2 hypoxic non-COVID-19 patients subjects who presented at the Masih Daneshvari Hospital of Tehran, Iran between March–May 2020. Whole blood samples were harvested from patients and intracellular NO levels in 1 × 10(6) red blood cells (RBC) was measured by DAF staining using flow cytometry (FACS Calibour, BD, CA, USA). RESULTS: The Mean florescent of intensity for NO was significantly enhanced in COVID-19 patients compared with healthy control subjects (P ≤ 0.05). As a further control for whether hypoxia induced this higher intracellular NO, we evaluated the levels of NO inside RBC of hypoxic patients. No significant differences in NO levels were seen between the hypoxic and non-hypoxic control group. CONCLUSIONS: This pilot study demonstrates increased levels of intracellular NO in RBCs from COVID-19 patients. Future multi-centre studies should examine whether this is seen in a larger number of COVID-19 patients and whether NO therapy may be of use in these severe COVID-19 patients. BioMed Central 2020-10-16 /pmc/articles/PMC7563910/ /pubmed/33066765 http://dx.doi.org/10.1186/s12890-020-01310-8 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Mortaz, Esmaeil
Malkmohammad, Majid
Jamaati, Hamidreza
Naghan, Parisa Adimi
Hashemian, Seyed MohamadReza
Tabarsi, Payam
Varahram, Maohammad
Zaheri, Hamidreza
Chousein, Efsun Gonca Uğur
Folkerts, Gert
Adcock, Ian M.
Silent hypoxia: higher NO in red blood cells of COVID-19 patients
title Silent hypoxia: higher NO in red blood cells of COVID-19 patients
title_full Silent hypoxia: higher NO in red blood cells of COVID-19 patients
title_fullStr Silent hypoxia: higher NO in red blood cells of COVID-19 patients
title_full_unstemmed Silent hypoxia: higher NO in red blood cells of COVID-19 patients
title_short Silent hypoxia: higher NO in red blood cells of COVID-19 patients
title_sort silent hypoxia: higher no in red blood cells of covid-19 patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7563910/
https://www.ncbi.nlm.nih.gov/pubmed/33066765
http://dx.doi.org/10.1186/s12890-020-01310-8
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