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In silico, in vitro: antioxidant and antihepatotoxic activity of gnetol from Gnetum ula Brongn

[Image: see text] Introduction: Gnetum ula is a notable medicinal plant used to cure various ailments. The stem part of the plant is used traditionally to treat jaundice and other disorders. The present work is to investigate the in vitro hepatoprotective and antioxidant activity of ethanol extract...

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Autores principales: Jinadatta, Preetham, Rajshekarappa, Sharath, Sundera Raja Rao, Kiran, Pasura Subbaiah, Sujan Ganapathy, Shastri, Sudhesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tabriz University of Medical Sciences 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6879709/
https://www.ncbi.nlm.nih.gov/pubmed/31799160
http://dx.doi.org/10.15171/bi.2019.29
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author Jinadatta, Preetham
Rajshekarappa, Sharath
Sundera Raja Rao, Kiran
Pasura Subbaiah, Sujan Ganapathy
Shastri, Sudhesh
author_facet Jinadatta, Preetham
Rajshekarappa, Sharath
Sundera Raja Rao, Kiran
Pasura Subbaiah, Sujan Ganapathy
Shastri, Sudhesh
author_sort Jinadatta, Preetham
collection PubMed
description [Image: see text] Introduction: Gnetum ula is a notable medicinal plant used to cure various ailments. The stem part of the plant is used traditionally to treat jaundice and other disorders. The present work is to investigate the in vitro hepatoprotective and antioxidant activity of ethanol extract of stem of G. ula (GUE) and its isolated compound gnetol. Methods: Column chromatography was carried out for GUE and various column fractions were obtained. DPPH and reducing power assays were performed for GUE and column fractions. The potent fraction was characterized, interpreted and tested for in vitro hepatoprotective activity on the BRL3A cell line. In silico docking studies of gnetol compound on the protein TGF-β (transforming growth factor – β) and Peroxisome proliferator-activated receptor α (PPARα) was carried out. Results: DPPH scavenging and reducing power assay showed that the fourth column fraction has antioxidant potential than other fractions. The fourth column fraction was characterized to obtain gnetol compound. BRL3A cell line was used for the toxicity study of GUE and gnetol. Both, the extract and the isolated compound were found to be nontoxic with CTC(50) value more than 1000 µg/mL. At the concentration of 200 µg/mL, GUE and gnetol offered cell protection of 50.2% and 54.3%, however, silymarin showed 77.15% protection at 200 µg/mL concentration against CCl(4) treated BRL3A cell line. The docking results of the ligand molecule TGF-β showed that gnetol has the binding affinity of -7.0 and standard silymarin being -6.8. TGF-β showed good hydrophobic interactions and formed two hydrogen bonds with the amino acids. For PPARα protein, gnetol showed the binding affinity of -8.4 and silymarin with -6.5. Hydrogen bonding and good hydrophobic interactions against the amino acid molecules in relation to the PPARα protein are shown. Conclusion: Gnetum ula stem extract and its isolated compound are safe and offered significant hepatoprotection against CCl4 induced toxicity. Isolated compound gnetol exhibited a potent antioxidant activity offering protection to liver damage. However, in vivo studies need to be carried out to validate the traditional use of G. ula .
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spelling pubmed-68797092019-12-03 In silico, in vitro: antioxidant and antihepatotoxic activity of gnetol from Gnetum ula Brongn Jinadatta, Preetham Rajshekarappa, Sharath Sundera Raja Rao, Kiran Pasura Subbaiah, Sujan Ganapathy Shastri, Sudhesh Bioimpacts Original Research [Image: see text] Introduction: Gnetum ula is a notable medicinal plant used to cure various ailments. The stem part of the plant is used traditionally to treat jaundice and other disorders. The present work is to investigate the in vitro hepatoprotective and antioxidant activity of ethanol extract of stem of G. ula (GUE) and its isolated compound gnetol. Methods: Column chromatography was carried out for GUE and various column fractions were obtained. DPPH and reducing power assays were performed for GUE and column fractions. The potent fraction was characterized, interpreted and tested for in vitro hepatoprotective activity on the BRL3A cell line. In silico docking studies of gnetol compound on the protein TGF-β (transforming growth factor – β) and Peroxisome proliferator-activated receptor α (PPARα) was carried out. Results: DPPH scavenging and reducing power assay showed that the fourth column fraction has antioxidant potential than other fractions. The fourth column fraction was characterized to obtain gnetol compound. BRL3A cell line was used for the toxicity study of GUE and gnetol. Both, the extract and the isolated compound were found to be nontoxic with CTC(50) value more than 1000 µg/mL. At the concentration of 200 µg/mL, GUE and gnetol offered cell protection of 50.2% and 54.3%, however, silymarin showed 77.15% protection at 200 µg/mL concentration against CCl(4) treated BRL3A cell line. The docking results of the ligand molecule TGF-β showed that gnetol has the binding affinity of -7.0 and standard silymarin being -6.8. TGF-β showed good hydrophobic interactions and formed two hydrogen bonds with the amino acids. For PPARα protein, gnetol showed the binding affinity of -8.4 and silymarin with -6.5. Hydrogen bonding and good hydrophobic interactions against the amino acid molecules in relation to the PPARα protein are shown. Conclusion: Gnetum ula stem extract and its isolated compound are safe and offered significant hepatoprotection against CCl4 induced toxicity. Isolated compound gnetol exhibited a potent antioxidant activity offering protection to liver damage. However, in vivo studies need to be carried out to validate the traditional use of G. ula . Tabriz University of Medical Sciences 2019 2019-05-22 /pmc/articles/PMC6879709/ /pubmed/31799160 http://dx.doi.org/10.15171/bi.2019.29 Text en © 2019 The Author(s) This work is published by BioImpacts as an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/). Non-commercial uses of the work are permitted, provided the original work is properly cited.
spellingShingle Original Research
Jinadatta, Preetham
Rajshekarappa, Sharath
Sundera Raja Rao, Kiran
Pasura Subbaiah, Sujan Ganapathy
Shastri, Sudhesh
In silico, in vitro: antioxidant and antihepatotoxic activity of gnetol from Gnetum ula Brongn
title In silico, in vitro: antioxidant and antihepatotoxic activity of gnetol from Gnetum ula Brongn
title_full In silico, in vitro: antioxidant and antihepatotoxic activity of gnetol from Gnetum ula Brongn
title_fullStr In silico, in vitro: antioxidant and antihepatotoxic activity of gnetol from Gnetum ula Brongn
title_full_unstemmed In silico, in vitro: antioxidant and antihepatotoxic activity of gnetol from Gnetum ula Brongn
title_short In silico, in vitro: antioxidant and antihepatotoxic activity of gnetol from Gnetum ula Brongn
title_sort in silico, in vitro: antioxidant and antihepatotoxic activity of gnetol from gnetum ula brongn
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6879709/
https://www.ncbi.nlm.nih.gov/pubmed/31799160
http://dx.doi.org/10.15171/bi.2019.29
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