Atish Gheware1,2,3,4, Dhwani Dholakia1,3,4, Sadasivam Kannan5, Lipsa Panda6,4, Ritu Rani1,2,3,4, Bijay Ranjan Pattnaik6, Vaibhav Jain6,4, Yash Parekh7, M Ghalib Enayathullah7, Kiran Kumar Bokara7,4, Venkatesan Subramanian5,4, Mitali Mukerji1,2,3,4, Anurag Agrawal8,9, Bhavana Prasher10,11,12,13. 1. Genomics and Molecular Medicine, Council of Scientific and Industrial Research -Institute of Genomics and Integrative Biology (CSIR-IGIB), Delhi, 110007, India. 2. CSIR's Ayurgenomics Unit-TRISUTRA (Translational Research and Innovative Science ThRoughAyurgenomics) CSIR-IGIB, Delhi, 110007, India. 3. Centre of Excellence for Applied Development of Ayurveda, Prakriti and Genomics, CSIR's Ayurgenomics Unit-TRISUTRA (Translational Research and Innovative Science ThRoughAyurgenomics), CSIR- IGIB, Delhi, 110007, India. 4. Academy of Scientific and Innovative Research (AcSIR), Ghaziabad, 201002, India. 5. Center for High Computing, CSIR- Central Leather Research Institute (CLRI), Chennai, 600020, India. 6. Center for Translational Research in Lung Disease, CSIR- IGIB, Delhi, 110007, India. 7. CSIR-Center for Cellular and Molecular Biology, Annexe-II, Medical Biotechnology Complex, Uppal Road, Hyderabad, Telangana, 500007, India. 8. Center for Translational Research in Lung Disease, CSIR- IGIB, Delhi, 110007, India. a.agrawal@igib.in. 9. Academy of Scientific and Innovative Research (AcSIR), Ghaziabad, 201002, India. a.agrawal@igib.in. 10. Genomics and Molecular Medicine, Council of Scientific and Industrial Research -Institute of Genomics and Integrative Biology (CSIR-IGIB), Delhi, 110007, India. bhavana.p@igib.res.in. 11. CSIR's Ayurgenomics Unit-TRISUTRA (Translational Research and Innovative Science ThRoughAyurgenomics) CSIR-IGIB, Delhi, 110007, India. bhavana.p@igib.res.in. 12. Centre of Excellence for Applied Development of Ayurveda, Prakriti and Genomics, CSIR's Ayurgenomics Unit-TRISUTRA (Translational Research and Innovative Science ThRoughAyurgenomics), CSIR- IGIB, Delhi, 110007, India. bhavana.p@igib.res.in. 13. Academy of Scientific and Innovative Research (AcSIR), Ghaziabad, 201002, India. bhavana.p@igib.res.in.
Abstract
BACKGROUND: COVID-19 pneumonia has been associated with severe acute hypoxia, sepsis-like states, thrombosis and chronic sequelae including persisting hypoxia and fibrosis. The molecular hypoxia response pathway has been associated with such pathologies and our recent observations on anti-hypoxic and anti-inflammatory effects of whole aqueous extract of Adhatoda Vasica (AV) prompted us to explore its effects on relevant preclinical mouse models. METHODS: In this study, we tested the effect of whole aqueous extract of AV, in murine models of bleomycin induced pulmonary fibrosis, Cecum Ligation and Puncture (CLP) induced sepsis, and siRNA induced hypoxia-thrombosis phenotype. The effect on lung of AV treated naïve mice was also studied at transcriptome level. We also determined if the extract may have any effect on SARS-CoV2 replication. RESULTS: Oral administration AV extract attenuates increased airway inflammation, levels of transforming growth factor-β1 (TGF-β1), IL-6, HIF-1α and improves the overall survival rates of mice in the models of pulmonary fibrosis and sepsis and rescues the siRNA induced inflammation and associated blood coagulation phenotypes in mice. We observed downregulation of hypoxia, inflammation, TGF-β1, and angiogenesis genes and upregulation of adaptive immunity-related genes in the lung transcriptome. AV treatment also reduced the viral load in Vero cells infected with SARS-CoV2. CONCLUSION: Our results provide a scientific rationale for this ayurvedic herbal medicine in ameliorating the hypoxia-hyperinflammation features and highlights the repurposing potential of AV in COVID-19-like conditions.
BACKGROUND:COVID-19 pneumonia has been associated with severe acute hypoxia, sepsis-like states, thrombosis and chronic sequelae including persisting hypoxia and fibrosis. The molecular hypoxia response pathway has been associated with such pathologies and our recent observations on anti-hypoxic and anti-inflammatory effects of whole aqueous extract of Adhatoda Vasica (AV) prompted us to explore its effects on relevant preclinical mouse models. METHODS: In this study, we tested the effect of whole aqueous extract of AV, in murine models of bleomycin induced pulmonary fibrosis, Cecum Ligation and Puncture (CLP) induced sepsis, and siRNA induced hypoxia-thrombosisphenotype. The effect on lung of AV treated naïve mice was also studied at transcriptome level. We also determined if the extract may have any effect on SARS-CoV2 replication. RESULTS: Oral administration AV extract attenuates increased airway inflammation, levels of transforming growth factor-β1 (TGF-β1), IL-6, HIF-1α and improves the overall survival rates of mice in the models of pulmonary fibrosis and sepsis and rescues the siRNA induced inflammation and associated blood coagulationphenotypes in mice. We observed downregulation of hypoxia, inflammation, TGF-β1, and angiogenesis genes and upregulation of adaptive immunity-related genes in the lung transcriptome. AV treatment also reduced the viral load in Vero cells infected with SARS-CoV2. CONCLUSION: Our results provide a scientific rationale for this ayurvedic herbal medicine in ameliorating the hypoxia-hyperinflammation features and highlights the repurposing potential of AV in COVID-19-like conditions.
Authors: Min Lang; Avik Som; Dexter P Mendoza; Efren J Flores; Nicholas Reid; Denston Carey; Matthew D Li; Alison Witkin; Josanna M Rodriguez-Lopez; Jo-Anne O Shepard; Brent P Little Journal: Lancet Infect Dis Date: 2020-04-30 Impact factor: 25.071
Authors: Ana Campos Codo; Gustavo Gastão Davanzo; Lauar de Brito Monteiro; Gabriela Fabiano de Souza; Stéfanie Primon Muraro; João Victor Virgilio-da-Silva; Juliana Silveira Prodonoff; Victor Corasolla Carregari; Carlos Alberto Oliveira de Biagi Junior; Fernanda Crunfli; Jeffersson Leandro Jimenez Restrepo; Pedro Henrique Vendramini; Guilherme Reis-de-Oliveira; Karina Bispo Dos Santos; Daniel A Toledo-Teixeira; Pierina Lorencini Parise; Matheus Cavalheiro Martini; Rafael Elias Marques; Helison R Carmo; Alexandre Borin; Laís Durço Coimbra; Vinícius O Boldrini; Natalia S Brunetti; Andre S Vieira; Eli Mansour; Raisa G Ulaf; Ana F Bernardes; Thyago A Nunes; Luciana C Ribeiro; Andre C Palma; Marcus V Agrela; Maria Luiza Moretti; Andrei C Sposito; Fabrício Bíscaro Pereira; Licio Augusto Velloso; Marco Aurélio Ramirez Vinolo; André Damasio; José Luiz Proença-Módena; Robson Francisco Carvalho; Marcelo A Mori; Daniel Martins-de-Souza; Helder I Nakaya; Alessandro S Farias; Pedro M Moraes-Vieira Journal: Cell Metab Date: 2020-07-17 Impact factor: 27.287