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In vitro biological assessment of Homalium zeylanicum and isolation of lucidenic acid A triterpenoid
Homalium zeylanicum (Gardner) Benth. (Flacourtiaceae) is a medicinal plant useful in controlling rheumatism, inflammation and diabetes. The objective of this work evaluates in vitro antioxidant, antidiabetic, and antiinflammatory properties of hydroalcohol extract of bark of H. zeylanicum (HAHZ). It...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Elsevier
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5615128/ https://www.ncbi.nlm.nih.gov/pubmed/28959649 http://dx.doi.org/10.1016/j.toxrep.2017.04.004 |
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author | Sahoo, Atish Kumar Dash, Umesh Chandra Kanhar, Satish Mahapatra, Ajay Kumar |
author_facet | Sahoo, Atish Kumar Dash, Umesh Chandra Kanhar, Satish Mahapatra, Ajay Kumar |
author_sort | Sahoo, Atish Kumar |
collection | PubMed |
description | Homalium zeylanicum (Gardner) Benth. (Flacourtiaceae) is a medicinal plant useful in controlling rheumatism, inflammation and diabetes. The objective of this work evaluates in vitro antioxidant, antidiabetic, and antiinflammatory properties of hydroalcohol extract of bark of H. zeylanicum (HAHZ). It also describes isolation and structure determination of lucidenic acid A, which is the first report in this plant. In order to explain the role of antioxidant principles, DPPH, nitric oxide, hydroxyl, superoxide and metal chelating assays were performed. Antidiabetic and anti-inflammatory activities were investigated by quantifying α-amylase, α-glucosidase and protein denaturation inhibitory activities of HAHZ. Biochemical estimations were performed. The chemical structure of the triterpenoid was elucidated using (1)H, (13)C NMR and high resolution-MS. IC(50) of DPPH, nitric oxide, hydroxyl, superoxide and metal chelating activities were of 36.23 ± 0.27, 40.11 ± 0.32, 35.23 ± 0.57, 43.34 ± 0.22 and 11.54 ± 0.08 μg/mL, respectively. IC(50) of α-amylase and α-glucosidase activities were 29.12 ± 0.54, and 18.55 ± 0.15 μg/mL. Total phenolic and total flavonoid contents were recorded at 233.65 mg/g GAE and 172.7 mg/g QE. Regarding kinetic behaviour, HAHZ showed competitive inhibition on α-glucosidase and mixed competitive inhibition on α-amylase. Lucidenic acid A was confirmed by spectroscopic studies. Anti-inflammatory activity of lucidenic acid A was determined by using protein denaturation assay with IC(50) 13 μg/mL but HAHZ showed 30.34 ± 0.13 μg/mL. Phenols and flavonoids could be attributed to inhibition of intestinal carbohydrases for anti-diabetic activities whereas triterpenoids could be responsible for anti-inflammatory activity of H. zeylanicum. |
format | Online Article Text |
id | pubmed-5615128 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-56151282017-09-28 In vitro biological assessment of Homalium zeylanicum and isolation of lucidenic acid A triterpenoid Sahoo, Atish Kumar Dash, Umesh Chandra Kanhar, Satish Mahapatra, Ajay Kumar Toxicol Rep Article Homalium zeylanicum (Gardner) Benth. (Flacourtiaceae) is a medicinal plant useful in controlling rheumatism, inflammation and diabetes. The objective of this work evaluates in vitro antioxidant, antidiabetic, and antiinflammatory properties of hydroalcohol extract of bark of H. zeylanicum (HAHZ). It also describes isolation and structure determination of lucidenic acid A, which is the first report in this plant. In order to explain the role of antioxidant principles, DPPH, nitric oxide, hydroxyl, superoxide and metal chelating assays were performed. Antidiabetic and anti-inflammatory activities were investigated by quantifying α-amylase, α-glucosidase and protein denaturation inhibitory activities of HAHZ. Biochemical estimations were performed. The chemical structure of the triterpenoid was elucidated using (1)H, (13)C NMR and high resolution-MS. IC(50) of DPPH, nitric oxide, hydroxyl, superoxide and metal chelating activities were of 36.23 ± 0.27, 40.11 ± 0.32, 35.23 ± 0.57, 43.34 ± 0.22 and 11.54 ± 0.08 μg/mL, respectively. IC(50) of α-amylase and α-glucosidase activities were 29.12 ± 0.54, and 18.55 ± 0.15 μg/mL. Total phenolic and total flavonoid contents were recorded at 233.65 mg/g GAE and 172.7 mg/g QE. Regarding kinetic behaviour, HAHZ showed competitive inhibition on α-glucosidase and mixed competitive inhibition on α-amylase. Lucidenic acid A was confirmed by spectroscopic studies. Anti-inflammatory activity of lucidenic acid A was determined by using protein denaturation assay with IC(50) 13 μg/mL but HAHZ showed 30.34 ± 0.13 μg/mL. Phenols and flavonoids could be attributed to inhibition of intestinal carbohydrases for anti-diabetic activities whereas triterpenoids could be responsible for anti-inflammatory activity of H. zeylanicum. Elsevier 2017-06-04 /pmc/articles/PMC5615128/ /pubmed/28959649 http://dx.doi.org/10.1016/j.toxrep.2017.04.004 Text en © 2017 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Sahoo, Atish Kumar Dash, Umesh Chandra Kanhar, Satish Mahapatra, Ajay Kumar In vitro biological assessment of Homalium zeylanicum and isolation of lucidenic acid A triterpenoid |
title | In vitro biological assessment of Homalium zeylanicum and isolation of lucidenic acid A triterpenoid |
title_full | In vitro biological assessment of Homalium zeylanicum and isolation of lucidenic acid A triterpenoid |
title_fullStr | In vitro biological assessment of Homalium zeylanicum and isolation of lucidenic acid A triterpenoid |
title_full_unstemmed | In vitro biological assessment of Homalium zeylanicum and isolation of lucidenic acid A triterpenoid |
title_short | In vitro biological assessment of Homalium zeylanicum and isolation of lucidenic acid A triterpenoid |
title_sort | in vitro biological assessment of homalium zeylanicum and isolation of lucidenic acid a triterpenoid |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5615128/ https://www.ncbi.nlm.nih.gov/pubmed/28959649 http://dx.doi.org/10.1016/j.toxrep.2017.04.004 |
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