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In silico and in vitro studies of lupeol and iso-orientin as potential antidiabetic agents in a rat model

Background: In silico characterization can help to explain the interaction between molecules and predict three-dimensional structures. Various studies have confirmed the glucose-lowering effects of plant extracts, ie, lupeol and iso-orientin, which enable them to be used as antidiabetic agents. Purp...

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Autores principales: Malik, Arif, Jamil, Uzma, Butt, Tariq Tahir, Waquar, Sulayman, Gan, Siew Hua, Shafique, Hassan, Jafar, Tassadaq Hussain
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6510393/
https://www.ncbi.nlm.nih.gov/pubmed/31123393
http://dx.doi.org/10.2147/DDDT.S176698
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author Malik, Arif
Jamil, Uzma
Butt, Tariq Tahir
Waquar, Sulayman
Gan, Siew Hua
Shafique, Hassan
Jafar, Tassadaq Hussain
author_facet Malik, Arif
Jamil, Uzma
Butt, Tariq Tahir
Waquar, Sulayman
Gan, Siew Hua
Shafique, Hassan
Jafar, Tassadaq Hussain
author_sort Malik, Arif
collection PubMed
description Background: In silico characterization can help to explain the interaction between molecules and predict three-dimensional structures. Various studies have confirmed the glucose-lowering effects of plant extracts, ie, lupeol and iso-orientin, which enable them to be used as antidiabetic agents. Purpose: Aims of the present study were to evaluate the hypoglycemic activities of lupeol and iso-orientin in a rat model. The study proposed the effects of alloxan on blood glucose level, body weight, and oxidative stress. Materials and Methods: Thirty (n=30) Wistar albino rats were divided into six groups and were subjected to different combinations of the compounds. Levels of different stress markers, ie, malondialdehyde, superoxide dismutase, catalase, nitric oxide, glutathione, glutathione peroxide, glutathione reductase, and blood glucose levels were estimated with their respective methods. Whereas, for their in silico analysis, identified target proteins, GPR40, glucose-6-phosphatase, UCP2, glycogen phosphorylase, aldose reductase, and glucose transporter-4 were docked with lupeol and iso-orientin. Three-dimensional structures were predicted by ERRAT, Rampage, Verify3D, threading and homology approaches. Results: Blood glucose levels were significantly increased in rats receiving intraperitoneal injection of alloxan (208±6.94 mg/dL) as compared to controls (90±7.38 mg/dL). Infected rats were administered plant extracts; combined treatment of both extracts (lupeol+iso-orientin) significantly reduced the levels of blood glucose (129.06±6.29 mg/dL) and improved the antioxidant status. Fifteen structures of each selected protein were evaluated using various techniques. Consequently, satisfactory quality factors [GPR40 (96.41%), glucose-6-phosphatase (96.56%), UCP2 (72.56%), glycogen phosphorylase (87.24%), aldose reductase (82.46%), and glucose transporter-4 (94.29%)] were selected. Molecular docking revealed interacting residues, effective drug properties and their binding affinities (ie, −8.9 to −12.6 Kcal/mol). Conclusion: Results of the study affirmed the antidiabetic activities of lupeol and iso-orientin. Administration of these extracts (either individually or in combination) significantly reduced blood glucose levels and oxidative stress. Hence, it may be considered beneficial in the treatment of diabetes.
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spelling pubmed-65103932019-05-23 In silico and in vitro studies of lupeol and iso-orientin as potential antidiabetic agents in a rat model Malik, Arif Jamil, Uzma Butt, Tariq Tahir Waquar, Sulayman Gan, Siew Hua Shafique, Hassan Jafar, Tassadaq Hussain Drug Des Devel Ther Original Research Background: In silico characterization can help to explain the interaction between molecules and predict three-dimensional structures. Various studies have confirmed the glucose-lowering effects of plant extracts, ie, lupeol and iso-orientin, which enable them to be used as antidiabetic agents. Purpose: Aims of the present study were to evaluate the hypoglycemic activities of lupeol and iso-orientin in a rat model. The study proposed the effects of alloxan on blood glucose level, body weight, and oxidative stress. Materials and Methods: Thirty (n=30) Wistar albino rats were divided into six groups and were subjected to different combinations of the compounds. Levels of different stress markers, ie, malondialdehyde, superoxide dismutase, catalase, nitric oxide, glutathione, glutathione peroxide, glutathione reductase, and blood glucose levels were estimated with their respective methods. Whereas, for their in silico analysis, identified target proteins, GPR40, glucose-6-phosphatase, UCP2, glycogen phosphorylase, aldose reductase, and glucose transporter-4 were docked with lupeol and iso-orientin. Three-dimensional structures were predicted by ERRAT, Rampage, Verify3D, threading and homology approaches. Results: Blood glucose levels were significantly increased in rats receiving intraperitoneal injection of alloxan (208±6.94 mg/dL) as compared to controls (90±7.38 mg/dL). Infected rats were administered plant extracts; combined treatment of both extracts (lupeol+iso-orientin) significantly reduced the levels of blood glucose (129.06±6.29 mg/dL) and improved the antioxidant status. Fifteen structures of each selected protein were evaluated using various techniques. Consequently, satisfactory quality factors [GPR40 (96.41%), glucose-6-phosphatase (96.56%), UCP2 (72.56%), glycogen phosphorylase (87.24%), aldose reductase (82.46%), and glucose transporter-4 (94.29%)] were selected. Molecular docking revealed interacting residues, effective drug properties and their binding affinities (ie, −8.9 to −12.6 Kcal/mol). Conclusion: Results of the study affirmed the antidiabetic activities of lupeol and iso-orientin. Administration of these extracts (either individually or in combination) significantly reduced blood glucose levels and oxidative stress. Hence, it may be considered beneficial in the treatment of diabetes. Dove 2019-05-06 /pmc/articles/PMC6510393/ /pubmed/31123393 http://dx.doi.org/10.2147/DDDT.S176698 Text en © 2019 Malik et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Malik, Arif
Jamil, Uzma
Butt, Tariq Tahir
Waquar, Sulayman
Gan, Siew Hua
Shafique, Hassan
Jafar, Tassadaq Hussain
In silico and in vitro studies of lupeol and iso-orientin as potential antidiabetic agents in a rat model
title In silico and in vitro studies of lupeol and iso-orientin as potential antidiabetic agents in a rat model
title_full In silico and in vitro studies of lupeol and iso-orientin as potential antidiabetic agents in a rat model
title_fullStr In silico and in vitro studies of lupeol and iso-orientin as potential antidiabetic agents in a rat model
title_full_unstemmed In silico and in vitro studies of lupeol and iso-orientin as potential antidiabetic agents in a rat model
title_short In silico and in vitro studies of lupeol and iso-orientin as potential antidiabetic agents in a rat model
title_sort in silico and in vitro studies of lupeol and iso-orientin as potential antidiabetic agents in a rat model
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6510393/
https://www.ncbi.nlm.nih.gov/pubmed/31123393
http://dx.doi.org/10.2147/DDDT.S176698
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