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Ex-vivo mucolytic and anti-inflammatory activity of BromAc in tracheal aspirates from COVID-19.
Coelho Dos Reis, Jordana Grazziela A; Ferreira, Geovane Marques; Lourenço, Alice Aparecida; Ribeiro, Ágata Lopes; da Mata, Camila Pacheco da Silveira Martins; de Melo Oliveira, Patrícia; Marques, Daisymara Priscila de Almeida; Ferreira, Linziane Lopes; Clarindo, Felipe Alves; da Silva, Murillo Ferreira; Filho, Heitor Portella Póvoas; Oliveira, Nilson Roberto Ribeiro; Sodré, Maisah Meyhr D'Carmo; Gadelha, Sandra Rocha; Albuquerque, George Rego; Maciel, Bianca Mendes; Mariano, Ana Paula Melo; Silva, Mylene de Melo; Fontana, Renato; Marin, Lauro Juliano; Carlos, Renata Santiago Alberto; Lopes, Amanda Teixeira Sampaio; Ferreira, Fabrício Barbosa; Dos Santos, Uener Ribeiro; Santana, Íris Terezinha Santos de; Fehlberg, Hllytchaikra Ferraz; Rezende, Rachel Passos; Dias, João Carlos T; Gross, Eduardo; Goulart, Gisele Assis Castro; Santiago, Marie Gabriele; de Lemos, Ana Paula Motta Lavigne; da Conceição, Aline O; Romano, Carla Cristina; de Carvalho, Luciana Debortoli; Martins Filho, Olindo Assis; Quadros, Claudio Almeida; Morris, David L; Valle, Sarah J.
  • Coelho Dos Reis JGA; Basic and Applied Virology Laboratory, Department of Microbiology, Institute for Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil. Electronic address: jreis@icb.ufmg.br.
  • Ferreira GM; Basic and Applied Virology Laboratory, Department of Microbiology, Institute for Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
  • Lourenço AA; Basic and Applied Virology Laboratory, Department of Microbiology, Institute for Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
  • Ribeiro ÁL; Basic and Applied Virology Laboratory, Department of Microbiology, Institute for Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
  • da Mata CPDSM; Risoleta Tolentino Neves Hospital, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
  • de Melo Oliveira P; Basic and Applied Virology Laboratory, Department of Microbiology, Institute for Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
  • Marques DPA; Basic and Applied Virology Laboratory, Department of Microbiology, Institute for Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
  • Ferreira LL; Basic and Applied Virology Laboratory, Department of Microbiology, Institute for Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
  • Clarindo FA; Basic and Applied Virology Laboratory, Department of Microbiology, Institute for Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
  • da Silva MF; Department of Biological Sciences, Santa Cruz State University, Ilhéus, BA, Brazil; Laboratory of Pharmacogenomics and Molecular Epidemiology (LAFEM), Santa Cruz State University (UESC), Ilhéus, BA, Brazil.
  • Filho HPP; Hospital de Ilhéus, Ilhéus, BA, Brazil.
  • Oliveira NRR; Hospital de Ilhéus, Ilhéus, BA, Brazil.
  • Sodré MMD; Laboratory of Pharmacogenomics and Molecular Epidemiology (LAFEM), Santa Cruz State University (UESC), Ilhéus, BA, Brazil.
  • Gadelha SR; Department of Biological Sciences, Santa Cruz State University, Ilhéus, BA, Brazil; Laboratory of Pharmacogenomics and Molecular Epidemiology (LAFEM), Santa Cruz State University (UESC), Ilhéus, BA, Brazil.
  • Albuquerque GR; Laboratory of Pharmacogenomics and Molecular Epidemiology (LAFEM), Santa Cruz State University (UESC), Ilhéus, BA, Brazil; Department of Agricultural and Environmental Sciences (DCAA), Santa Cruz State University (UESC), Ilhéus, BA, Brazil.
  • Maciel BM; Department of Biological Sciences, Santa Cruz State University, Ilhéus, BA, Brazil; Laboratory of Pharmacogenomics and Molecular Epidemiology (LAFEM), Santa Cruz State University (UESC), Ilhéus, BA, Brazil.
  • Mariano APM; Department of Biological Sciences, Santa Cruz State University, Ilhéus, BA, Brazil; Laboratory of Pharmacogenomics and Molecular Epidemiology (LAFEM), Santa Cruz State University (UESC), Ilhéus, BA, Brazil.
  • Silva MM; Laboratory of Pharmacogenomics and Molecular Epidemiology (LAFEM), Santa Cruz State University (UESC), Ilhéus, BA, Brazil.
  • Fontana R; Department of Biological Sciences, Santa Cruz State University, Ilhéus, BA, Brazil; Laboratory of Pharmacogenomics and Molecular Epidemiology (LAFEM), Santa Cruz State University (UESC), Ilhéus, BA, Brazil.
  • Marin LJ; Laboratory of Pharmacogenomics and Molecular Epidemiology (LAFEM), Santa Cruz State University (UESC), Ilhéus, BA, Brazil; Department of Health Sciences (DCS), Santa Cruz State University (UESC), Ilhéus, BA, Brazil.
  • Carlos RSA; Department of Agricultural and Environmental Sciences (DCAA), Santa Cruz State University (UESC), Ilhéus, BA, Brazil.
  • Lopes ATS; Laboratory of Pharmacogenomics and Molecular Epidemiology (LAFEM), Santa Cruz State University (UESC), Ilhéus, BA, Brazil.
  • Ferreira FB; Laboratory of Pharmacogenomics and Molecular Epidemiology (LAFEM), Santa Cruz State University (UESC), Ilhéus, BA, Brazil.
  • Dos Santos UR; Department of Biological Sciences, Santa Cruz State University, Ilhéus, BA, Brazil.
  • Santana ÍTS; Laboratory of Pharmacogenomics and Molecular Epidemiology (LAFEM), Santa Cruz State University (UESC), Ilhéus, BA, Brazil.
  • Fehlberg HF; Laboratory of Pharmacogenomics and Molecular Epidemiology (LAFEM), Santa Cruz State University (UESC), Ilhéus, BA, Brazil.
  • Rezende RP; Department of Biological Sciences, Santa Cruz State University, Ilhéus, BA, Brazil.
  • Dias JCT; Department of Biological Sciences, Santa Cruz State University, Ilhéus, BA, Brazil.
  • Gross E; Department of Biological Sciences, Santa Cruz State University, Ilhéus, BA, Brazil.
  • Goulart GAC; Department of Pharmaceuticals, Faculty of Pharmacy, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
  • Santiago MG; Department of Pharmaceuticals, Faculty of Pharmacy, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
  • de Lemos APML; Hospital de Ilhéus, Ilhéus, BA, Brazil.
  • da Conceição AO; Department of Biological Sciences, Santa Cruz State University, Ilhéus, BA, Brazil.
  • Romano CC; Hospital de Ilhéus, Ilhéus, BA, Brazil.
  • de Carvalho LD; Department of Biological Sciences, Santa Cruz State University, Ilhéus, BA, Brazil.
  • Martins Filho OA; Grupo Integrado de Pesquisas em Biomarcadores, Instituto René Rachou, Fiocruz Minas, Belo Horizonte, MG, Brazil.
  • Quadros CA; São Rafael Hospital and Bahia State University, Salvador, Bahia, Brazil.
  • Morris DL; Mucpharm Pty Ltd, Sydney, NSW, Australia; University of New South Wales, St George & Sutherland Hospital Clinical School, Sydney, NSW, Australia; Department of Surgery, St George Hospital, Sydney, NSW, Australia. Electronic address: david.morris@unsw.edu.au.
  • Valle SJ; Mucpharm Pty Ltd, Sydney, NSW, Australia; University of New South Wales, St George & Sutherland Hospital Clinical School, Sydney, NSW, Australia. Electronic address: sarah@mucpharm.com.
Biomed Pharmacother ; 148: 112753, 2022 04.
Article in English | MEDLINE | ID: covidwho-1707727
ABSTRACT
COVID-19 is a lethal disease caused by the pandemic SARS-CoV-2, which continues to be a public health threat. COVID-19 is principally a respiratory disease and is often associated with sputum retention and cytokine storm, for which there are limited therapeutic options. In this regard, we evaluated the use of BromAc®, a combination of Bromelain and Acetylcysteine (NAC). Both drugs present mucolytic effect and have been studied to treat COVID-19. Therefore, we sought to examine the mucolytic and anti-inflammatory effect of BromAc® in tracheal aspirate samples from critically ill COVID-19 patients requiring mechanical ventilation.

METHOD:

Tracheal aspirate samples from COVID-19 patients were collected following next of kin consent and mucolysis, rheometry and cytokine analysis using Luminex kit was performed.

RESULTS:

BromAc® displayed a robust mucolytic effect in a dose dependent manner on COVID-19 sputum ex vivo. BromAc® showed anti-inflammatory activity, reducing the action of cytokine storm, chemokines including MIP-1alpha, CXCL8, MIP-1b, MCP-1 and IP-10, and regulatory cytokines IL-5, IL-10, IL-13 IL-1Ra and total reduction for IL-9 compared to NAC alone and control. BromAc® acted on IL-6, demonstrating a reduction in G-CSF and VEGF-D at concentrations of 125 and 250 µg.

CONCLUSION:

These results indicate robust mucolytic and anti-inflammatory effect of BromAc® ex vivo in tracheal aspirates from critically ill COVID-19 patients, indicating its potential to be further assessed as pharmacological treatment for COVID-19.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Acetylcysteine / Sputum / Bromelains / Cytokines / Chemokines / COVID-19 Type of study: Experimental Studies Limits: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged / Young adult Language: English Journal: Biomed Pharmacother Year: 2022 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Acetylcysteine / Sputum / Bromelains / Cytokines / Chemokines / COVID-19 Type of study: Experimental Studies Limits: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged / Young adult Language: English Journal: Biomed Pharmacother Year: 2022 Document Type: Article